Global Variome shared LOVD
TAB2 (TGF-beta activated kinase 1/MAP3K7 binding pr...)
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The variants shown are described using the
NM_015093.4
NM_001292034.2
transcript reference sequence.
Legend
Please note that a short description of a certain column can be displayed when you move your mouse cursor over the column's header and hold it still. Below, a more detailed description is shown per column.
Effect
: The variant's effect on the function of the gene/protein, displayed in the format 'R/C'. R is the value reported by the source (publication, submitter) and this classification may vary between records. C is the value concluded by the curator. Note that in some database the curator uses Summary records to give details on the classification of the variant.Values used: '+' indicating the variant affects function, '+?' probably affects function, '-' does not affect function, '-?' probably does not affect function, '?' effect unknown, '.' effect was not classified.
Exon
: number of exon/intron containing variant; 2 = exon 2, 12i = intron 12, 2i_7i = from intron 2 to intron 7, 8i_9 = intron 8/exon 9 boundary, _1 = 5' to exon 1, 18_ = 3' of exon 18, _1_18_ = encompassing the entire 18-exon gene
DNA change (cDNA)
: description of variant at DNA level, based on a coding DNA reference sequence (following HGVS recommendations); e.g. c.123C>T, c.123_145del, c.123_126dup. For deletions/duplications extending beyond the reference transcript resp. {0}/{2} is used to replace del/dup. Extent of the deletion/duplication should be specified using the genomic description (g.). "-" indicates the variant described on genomic level does not affect the coding DNA reference sequence.
RNA change
: description of variant at RNA level (following HGVS recommendations).
r.123c>u
r.? = unknown
r.(?) = RNA not analysed but probably transcribed copy of DNA variant
r.spl? = RNA not analysed but variant probably affects splicing
r.(spl?) = RNA not analysed but variant may affect splicing
r.0? = change expected to abolish transcription
Protein
: description of variant at protein level (following HGVS recommendations).
p.(Arg345Pro) = change predicted from DNA (RNA not analysed)
p.Arg345Pro = change derived from RNA analysis
p.? = unknown effect
p.0? = probably no protein produced
Allele
: On which allele is the variant located? Does not necessarily imply inheritance! 'Paternal' (confirmed or inferred), 'Maternal' (confirmed or inferred), 'Parent #1' or #2 for compound heterozygosity without having screened the parents, 'Unknown' for heterozygosity without having screened the parents, 'Both' for homozygozity.
Classification method
: The method used for the clinical classification of this variant.
All options:
ACMG
ACGS
EAHAD-CFDB
ENIGMA
IARC
InSiGHT
kConFab
other
Clinical classification
: Clinical classification of variant, preferably based on standardised criteria (e.g. ACMG), directed on the clinical consequences as published/submitted, indicated using an enriched system including inheritance: e.g. pathogenic, pathogenic (dominant), pathogenic (recessive), pathogenic (!), pathogenic (maternal), pathogenic (paternal). Standard inheritance is covered by dominant/recessive, imprinting by maternal/paternal. A '!' warns for exceptional circumstances to be explained in the 'Remarks' field (low penetrance, variants pathogenic in heterozygous state only, hypomorphic/hypermorphic variants, protective variants, etc.). Non-disease consequences (e.g. drug metabolism (pharmacogenetics), risk factor, blood group, tasting bitter) are indicated using additions to the benign classification; benign (dominant), benign (recessive), benign (!), etc. The value 'association' is used for variants associated with a phenotype and 'NA' for variants from in vitro/in silico records. NOTE: classification may differ from the opinion of the curator as given in a variant SUMMARY-record or the 'Functional effect concluded'). NOTE: pathogenic/likely pathogenic should go together with "variant (probably) affects function" In ClassFunctional.
All options:
pathogenic
pathogenic (dominant)
pathogenic (recessive)
pathogenic (!)
pathogenic (maternal)
pathogenic (paternal)
likely pathogenic
likely pathogenic (dominant)
likely pathogenic (recessive)
likely pathogenic (!)
likely pathogenic (maternal)
likely pathogenic (paternal)
VUS
VUS (!)
likely benign
likely benign (dominant)
likely benign (recessive)
likely benign (!)
likely benign (maternal)
likely benign (paternal)
benign
benign (dominant)
benign (recessive)
benign (!)
benign (maternal)
benign (paternal)
conflicting
association
NA
DNA change (genomic) (hg19)
: HGVS description of variant at DNA level, based on the genomic (chromosomal) DNA reference sequence; e.g. g.12345678C>T, g.12345679del, g.12345678_12345890dup
DNA change (hg38)
: HGVS description of variant at DNA level, based on the hg38 genomic (chromosomal) eference sequence; e.g. g.12345678C>T, g.12345679del, g.12345678_12345890dup
Published as
: listed only when different from "DNA change"; variant as reported originally (e.g. 521delT). Variants seen in animal models, tested in vitro, predicted from RNA analysis, etc. are described between brackets like c.(456C>G)
ISCN
: description of the variant according to ISCN nomenclature
DB-ID
: database ID of variant, grouping multiple observations of the same variant together, starting with the HGNC gene symbol, followed by an underscore (_) and a six digit number (e.g. DMD_012345). _000000 is used for variants where DNA was not analysed (change predicted from RNA analysis), variants seen in animal models or variants not seen in humans but functionally tested in vitro
Variant remarks
: remarks regarding variant described, e.g. germline mosaicism in mother, 345 kb deletion, muscle RNA analysed, not in 200 control chromosomes tested, on founder haplotype, etc.
Reference
: publication describing the variant submitted, incl. links to OMIM, PubMed or other source, e.g. "den Dunnen ASHG2003 P2346"
ClinVar ID
: ID of variant in ClinVar database
dbSNP ID
: the dbSNP ID
Origin
: Origin of variant/record: Germline = in all cells, De novo = in all cells, but not in either parent, Germline/De novo (untested) = in all cells, parents not tested (use only when De novo is likely, e.g. isolated/sporadic cases with dominant disease), Somatic = present in a subset of cells, but not in either parent, Uniparental disomy = from parental disomy (maternal or paternal), CLASSIFICATION record = submitter only sharing variant classification (note another report may share Individual data), SUMMARY record = master summary record from curator (may link to another database), In vitro (cloned) = data resulting from in vitro functional assays, animal model = data from animal model, Artefact = false positive variant call, DUPLICATE record = variant already described on another chromosome (e.g. unbalanced translocation, duplicating transposition, 2nd fusion transcript, etc.)
All options:
Germline
De novo
Germline/De novo (untested)
Somatic
Uniparental disomy
Uniparental disomy, maternal allele
Uniparental disomy, paternal allele
CLASSIFICATION record
SUMMARY record
In vitro (cloned)
In silico
animal model
Artefact
DUPLICATE record
Unknown
Not applicable
Segregation
: Indicates whether the variant segregates with the phenotype (yes), does not segregate with the phenotype (no) or segregation is unknown (?)
All options:
? = unknown
yes = segregates with phenotype
no = does not segregate with phenotype
- = not applicable
Frequency
: frequency in which the variant was found; e.g 5/760 chromosomes (in 5 of 760 chromosomes tested), 1/33 patients (in 1 of 33 patients analysed in study), 0.05 controls (in 5% of control cases tested)
Re-site
: restriction enzyme recognition site created (+) or destroyed (-); e.g. BglII+;BamHI-
VIP
: variant VIP-status was requested for matchmaking - need collaboration(s) to crack the case - please contact the submitter/curator. NOTE: to get VIP status ask the curator.
Methylation
: result of methylation test; GOM (gain of methylation), LOM (loss of methylation), 30% (30% methylated). NOTE: when several tests were done mention the method as well (e.g. MS-PCR 75%)
Template
: Template(s) used to detect the sequence variant; DNA (genomic DNA), RNA (cDNA) or protein
All options:
DNA
RNA = RNA (cDNA)
protein
? = unknown
Technique
: technique(s) used to identify the sequence variant.
All options:
? = unknown
ARMS = amplification refractory mutation system
arrayCGH = array for Comparative Genomic Hybridisation
arrayMET = array for methylation analysis
arraySEQ = array for resequencing
arraySNP = array for SNP typing
arrayCNV = array for Copy Number Variation (SNP and CNV probes)
ASO = allele-specific oligo hybridisation
BESS = Base Excision Sequence Scanning
CMC = Chemical Mismatch Cleavage
COBRA = Combined Bisulfite Restriction Analysis
CSCE = Conformation Sensitive Capillary Electrophoresis
CSGE = Conformation Sensitive Gel Electrophoresis
ddF = dideoxy Fingerprinting
DGGE = Denaturing-Gradient Gel-Electrophoresis
DHPLC = Denaturing High-Performance Liquid Chromatography
DOVAM = Detection Of Virtually All Mutations (SSCA variant)
DSCA = Double-Strand DNA Conformation Analysis
DSDI = Detection Small Deletions and Insertions
EMC = Enzymatic Mismatch Cleavage
expr = expression analysis
FISH = Fluorescent In-Situ Hybridisation
FISHf = fiberFISH
HD = HeteroDuplex analysis
HPLC = High-Performance Liquid Chromatography
IEF = IsoElectric Focussing
IHC = Immuno-Histo-Chemistry
Invader = Invader assay
MAPH = Multiplex Amplifiable Probe Hybridisation
MAQ = Multiplex Amplicon Quantification
MCA = Melting Curve Analysis, high-resolution (HRMA)
microscope = microscopic analysis (karyotype)
microsat = microsatellite genotyping
minigene = expression minigene construct
MIP = Molecular Inversion Probe amplification
MIPsm = single molecule Molecular Inversion Probe amplification
MLPA = Multiplex Ligation-dependent Probe Amplification
MLPA-ms = Multiplex Ligation-dependent Probe Amplification, methylation specific
MS = mass spectrometry
Northern = Northern blotting
NUC = nuclease digestion (RNAseT1, S1)
OM = optical mapping
PAGE = Poly-Acrylamide Gel-Electrophoresis
PCR = Polymerase Chain Reaction
PCRdd = PCR, digital droplet
PCRdig = PCR + restriction enzyme digestion
PCRh = PCR, haloplex
PCRlr = PCR, long-range
PCRm = PCR, multiplex
PCRms = PCR, methylation sensitive
PCRq = PCR, quantitative (qPCR)
PCRrp = PCR, repeat-primed (RP-PCR)
PCRsqd = PCR, semi-quantitative duplex
PE = primer extension (APEX, SNaPshot)
PEms = primer extension, methylation-sensitive single-nucleotide
PFGE = Pulsed-Field Gel-Electrophoresis (+Southern)
PTT = Protein Truncation Test
RFLP = Restriction Fragment Length Polymorphisms
RT-PCR = Reverse Transcription and PCR
RT-PCRq = Reverse Transcription and PCR, quantitative
SBE = Single Base Extension
SEQ = SEQuencing (Sanger)
SEQb = bisulfite SEQuencing
SEQp = pyroSequencing
SEQms = sequencing, methylation specific
SEQ-ON = next-generation sequencing - Oxford Nanopore
SEQ-NG = next-generation sequencing
SEQ-NG-RNA = next-generation sequencing RNA
SEQ-NG-H = next-generation sequencing - Helicos
SEQ-NG-I = next-generation sequencing - Illumina/Solexa
SEQ-NG-IT = next-generation sequencing - Ion Torrent
SEQ-NG-R = next-generation sequencing - Roche/454
SEQ-NG-S = next-generation sequencing - SOLiD
SEQ-PB = next-generation sequencing - Pacific Biosciences
SNPlex = SNPlex
Southern = Southern blotting
SSCA = Single-Strand DNA Conformation polymorphism Analysis (SSCP)
SSCAf = fluorescent SSCA (SSCP)
STR = Short Tandem Repeat
TaqMan = TaqMan assay
Western = Western blotting
- = not applicable
Tissue
: tissue type used for analysis
Remarks
: remarks regarding the screening like WGS (whole genome sequencing), WES (whole exome sequencing, gene panel (incl. a list of genes analysed), etc.
ID_report
: ID of the individual that can be publically shared, e.g. as listed in a publication
Reference
: reference to publication describing the individual/family, possibly giving more phenotypic details than listed in this database entry, incl. link to PubMed or other source, e.g. "den Dunnen ASHG2003 P2346"
Remarks
: remarks about the individual
Gender
: gender individual
All options:
? = unknown
- = not applicable
F = female
M = male
rF = raised as female
rM = raised as male
Consanguinity
: indicates whether the parents are related (consanguineous), not related (non-consanguineous) or whether consanguinity is not known (unknown)
All options:
no = non-consanguineous parents
yes = consanguineous parents
likely = consanguinity likely
? = unknown
- = not applicable
Country
: where (country) does the individual live/recently came from. Give additional details (population, specific sub-group) and when parents come from different countries in "Population". Belgium = individual lives in/recently came from Belgium, (France) = reported by laboratory in France, individual's country of origin not sure
All options:
? (unknown)
- (not applicable)
Afghanistan
(Afghanistan)
Albania
(Albania)
Algeria
(Algeria)
American Samoa
(American Samoa)
Andorra
(Andorra)
Angola
(Angola)
Anguilla
(Anguilla)
Antarctica
(Antarctica)
Antigua and Barbuda
(Antigua and Barbuda)
Argentina
(Argentina)
Armenia
(Armenia)
Aruba
(Aruba)
Australia
(Australia)
Austria
(Austria)
Azerbaijan
(Azerbaijan)
Bahamas
(Bahamas)
Bahrain
(Bahrain)
Bangladesh
(Bangladesh)
Barbados
(Barbados)
Belarus
(Belarus)
Belgium
(Belgium)
Belize
(Belize)
Benin
(Benin)
Bermuda
(Bermuda)
Bhutan
(Bhutan)
Bolivia
(Bolivia)
Bosnia and Herzegovina
(Bosnia and Herzegovina)
Botswana
(Botswana)
Bouvet Island
(Bouvet Island)
Brazil
(Brazil)
British Indian Ocean Territory
(British Indian Ocean Territory)
Brunei Darussalam
(Brunei Darussalam)
Bulgaria
(Bulgaria)
Burkina Faso
(Burkina Faso)
Burundi
(Burundi)
Cambodia
(Cambodia)
Cameroon
(Cameroon)
Canada
(Canada)
Cape Verde
(Cape Verde)
Cayman Islands
(Cayman Islands)
Central African Republic
(Central African Republic)
Central Europe
Chad
(Chad)
Chile
(Chile)
China
(China)
Christmas Island
(Christmas Island)
Cocos (Keeling Islands)
(Cocos (Keeling Islands))
Colombia
(Colombia)
Comoros
(Comoros)
Congo
(Congo)
Cook Islands
(Cook Islands)
Costa Rica
(Costa Rica)
Cote D'Ivoire (Ivory Coast)
(Cote D'Ivoire (Ivory Coast))
Croatia (Hrvatska)
(Croatia (Hrvatska))
Cuba
(Cuba)
Cyprus
(Cyprus)
Czech Republic
(Czech Republic)
Denmark
(Denmark)
Djibouti
(Djibouti)
Dominica
(Dominica)
Dominican Republic
(Dominican Republic)
East Timor
(East Timor)
Ecuador
(Ecuador)
Egypt
(Egypt)
El Salvador
(El Salvador)
England
(England)
Equatorial Guinea
(Equatorial Guinea)
Eritrea
(Eritrea)
Estonia
(Estonia)
Ethiopia
(Ethiopia)
Falkland Islands (Malvinas)
(Falkland Islands (Malvinas))
Faroe Islands
(Faroe Islands)
Fiji
(Fiji)
Finland
(Finland)
France
(France)
Gabon
(Gabon)
Gambia
(Gambia)
Georgia
(Georgia)
Germany
(Germany)
Ghana
(Ghana)
Gibraltar
(Gibraltar)
Greece
(Greece)
Greenland
(Greenland)
Grenada
(Grenada)
Guadeloupe
(Guadeloupe)
Guam
(Guam)
Guatemala
(Guatemala)
Guiana, French
(Guiana, French)
Guinea
(Guinea)
Guinea-Bissau
(Guinea-Bissau)
Guyana
(Guyana)
Haiti
(Haiti)
Heard and McDonald Islands
(Heard and McDonald Islands)
Honduras
(Honduras)
Hong Kong
(Hong Kong)
Hungary
(Hungary)
Iceland
(Iceland)
India
(India)
Indonesia
(Indonesia)
Iran
(Iran)
Iraq
(Iraq)
Ireland
(Ireland)
Israel
(Israel)
Italy
(Italy)
Jamaica
(Jamaica)
Japan
(Japan)
Jordan
(Jordan)
Kazakhstan
(Kazakhstan)
Kenya
(Kenya)
Kiribati
(Kiribati)
Korea
(Korea)
Korea, North (People's Republic)
(Korea, North (People's Republic))
Korea, South (Republic)
(Korea, South (Republic))
Kosovo
(Kosovo)
Kuwait
(Kuwait)
Kyrgyzstan (Kyrgyz Republic)
(Kyrgyzstan (Kyrgyz Republic))
Laos
(Laos)
Latvia
(Latvia)
Lebanon
(Lebanon)
Lesotho
(Lesotho)
Liberia
(Liberia)
Libya
(Libya)
Liechtenstein
(Liechtenstein)
Lithuania
(Lithuania)
Luxembourg
(Luxembourg)
Macau
(Macau)
Macedonia
(Macedonia)
Madagascar
(Madagascar)
Malawi
(Malawi)
Malaysia
(Malaysia)
Maldives
(Maldives)
Mali
(Mali)
Mallorca
(Mallorca)
Malta
(Malta)
Marshall Islands
(Marshall Islands)
Martinique
(Martinique)
Mauritania
(Mauritania)
Mauritius
(Mauritius)
Mayotte
(Mayotte)
Mexico
(Mexico)
Micronesia
(Micronesia)
Moldova
(Moldova)
Monaco
(Monaco)
Mongolia
(Mongolia)
Montserrat
(Montserrat)
Morocco
(Morocco)
Mozambique
(Mozambique)
Myanmar
(Myanmar)
Namibia
(Namibia)
Nauru
(Nauru)
Nepal
(Nepal)
Netherlands
(Netherlands)
Netherlands Antilles
(Netherlands Antilles)
Neutral Zone (Saudia Arabia/Iraq)
(Neutral Zone (Saudia Arabia/Iraq))
New Caledonia
(New Caledonia)
New Zealand
(New Zealand)
Nicaragua
(Nicaragua)
Niger
(Niger)
Nigeria
(Nigeria)
Niue
(Niue)
Norfolk Island
(Norfolk Island)
Northern Ireland
(Northern Ireland)
Northern Mariana Islands
(Northern Mariana Islands)
Norway
(Norway)
Oman
(Oman)
Pakistan
(Pakistan)
Palau
(Palau)
Palestine
(Palestine)
Panama
(Panama)
Papua New Guinea
(Papua New Guinea)
Paraguay
(Paraguay)
Peru
(Peru)
Philippines
(Philippines)
Pitcairn
(Pitcairn)
Poland
(Poland)
Polynesia, French
(Polynesia, French)
Portugal
(Portugal)
Puerto Rico
(Puerto Rico)
Qatar
(Qatar)
Reunion
(Reunion)
Romania
(Romania)
Russia
(Russia)
Russian Federation
(Russian Federation)
Rwanda
(Rwanda)
S. Georgia and S. Sandwich Isls.
(S. Georgia and S. Sandwich Isls.)
Saint Kitts and Nevis
(Saint Kitts and Nevis)
Saint Lucia
(Saint Lucia)
Saint Vincent and The Grenadines
(Saint Vincent and The Grenadines)
Samoa
(Samoa)
San Marino
(San Marino)
Sao Tome and Principe
(Sao Tome and Principe)
Saudi Arabia
(Saudi Arabia)
Scotland
(Scotland)
Senegal
(Senegal)
Serbia
(Serbia)
Seychelles
(Seychelles)
Sierra Leone
(Sierra Leone)
Singapore
(Singapore)
Slovakia (Slovak Republic)
(Slovakia (Slovak Republic))
Slovenia
(Slovenia)
Solomon Islands
(Solomon Islands)
Somalia
(Somalia)
South Africa
(South Africa)
Southern Territories, French
(Southern Territories, French)
Soviet Union (former)
(Soviet Union (former))
Spain
(Spain)
Sri Lanka
(Sri Lanka)
St. Helena, Ascension and Tristan da
Cunha
(St. Helena, Ascension and Tristan da
Cunha)
St. Pierre and Miquelon
(St. Pierre and Miquelon)
Sudan
(Sudan)
Sudan, South
(Sudan, South)
Suriname
(Suriname)
Svalbard and Jan Mayen Islands
(Svalbard and Jan Mayen Islands)
Swaziland
(Swaziland)
Sweden
(Sweden)
Switzerland
(Switzerland)
Syria
(Syria)
Taiwan
(Taiwan)
Tajikistan
(Tajikistan)
Tanzania
(Tanzania)
Thailand
(Thailand)
Togo
(Togo)
Tokelau
(Tokelau)
Tonga
(Tonga)
Trinidad and Tobago
(Trinidad and Tobago)
Tunisia
(Tunisia)
Turkey
(Turkey)
Turkmenistan
(Turkmenistan)
Turks and Caicos Islands
(Turks and Caicos Islands)
Tuvalu
(Tuvalu)
Uganda
(Uganda)
Ukraine
(Ukraine)
United Arab Emirates
(United Arab Emirates)
United Kingdom (Great Britain)
(United Kingdom (Great Britain))
United States
(United States)
Uruguay
(Uruguay)
US Minor Outlying Islands
(US Minor Outlying Islands)
Uzbekistan
(Uzbekistan)
Vanuatu
(Vanuatu)
Vatican City State (Holy See)
(Vatican City State (Holy See))
Venezuela
(Venezuela)
Viet Nam
(Viet Nam)
Virgin Islands (British)
(Virgin Islands (British))
Virgin Islands (US)
(Virgin Islands (US))
Wales
(Wales)
Wallis and Futuna Islands
(Wallis and Futuna Islands)
Western Sahara
(Western Sahara)
Yemen
(Yemen)
Yugoslavia
(Yugoslavia)
Zaire
(Zaire)
Zambia
(Zambia)
Zimbabwe
(Zimbabwe)
Population
: population the individual (or ancestors) belongs to; e.g. white, gypsy, Jewish-Ashkenazi, Africa-N, Sardinia, etc.
Age at death
: age at which the individual deceased (when applicable):
35y = 35 years
>43y = still alive at 43y
04y08m = 4 years and 8 months
00y00m01d12h = 1 day and 12 hours
18y? = around 18 years
30y-40y = between 30 and 40 years
>54y = older than 54
? = unknown
VIP
: individual/phenotype VIP-status was requested for matchmaking - need collaboration(s) to crack the case - please contact the submitter/curator. NOTE: to get VIP status ask the curator.
Data_av
: are additional data available upon request: e.g. pedigree (yes/no/?)
Treatment
: treatment of patient
How to query this table
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Operator
Column type
Example
Matches
Text
Arg
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space
Text
Arg Ser
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|
Text
Arg|Ser
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!
Text
!fs
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^
Text
^p.(Arg
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$
Text
Ser)$
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=""
Text
=""
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=""
Text
="p.0"
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!=""
Text
!=""
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!=""
Text
!="p.0"
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combination
Text
*|Ter !fs
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Date
2020
all entries matching the year 2020
|
Date
2020-03|2020-04
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!
Date
!2020-03
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<
Date
<2020
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<=
Date
<=2020-06
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>
Date
>2020-06
all entries after June, 2020
>=
Date
>=2020-06-15
all entries on or after June 15th, 2020
combination
Date
2019|2020 <2020-03
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Numeric
23
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|
Numeric
23|24
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!
Numeric
!23
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<
Numeric
<23
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<=
Numeric
<=23
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>
Numeric
>23
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>=
Numeric
>=23
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combination
Numeric
>=20 <30 !23
all entries with values from 20 to 29, but not equal to 23
Some more advanced examples:
Example
Matches
Asian
all entries containing 'Asian', 'asian', including 'Caucasian', 'caucasian', etc.
Asian !Caucasian
all entries containing 'Asian' but not containing 'Caucasian'
Asian|African !Caucasian
all entries containing 'Asian' or 'African', but not containing 'Caucasian'
"South Asian"
all entries containing 'South Asian', but not containing 'South East Asian'
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112 entries on 2 pages. Showing entries 1 - 100.
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Effect
Exon
DNA change (cDNA)
RNA change
Protein
Allele
Classification method
Clinical classification
DNA change (genomic) (hg19)
DNA change (hg38)
Published as
ISCN
DB-ID
Variant remarks
Reference
ClinVar ID
dbSNP ID
Origin
Segregation
Frequency
Re-site
VIP
Methylation
Template
Technique
Tissue
Remarks
Disease
ID_report
Reference
Remarks
Gender
Consanguinity
Country
Population
Age at death
VIP
Data_av
Treatment
Panel size
Owner
+/.
_1_9_
c.-421_*1892{0}
r.0
p.0
Unknown
-
pathogenic (dominant)
g.(?_149056337)_(151113208_?)del
-
149056337-151113208del
-
TAB2_000045
-
PubMed: Ritelli 2018
-
-
De novo
-
-
-
-
-
DNA
arrayCGH, SEQ-NG
-
WES
CHTD
Fam2Pat4
PubMed: Ritelli 2018
-
F
-
Italy
-
-
-
-
-
1
Johan den Dunnen
?/.
-
c.-100100A>G
r.(?)
p.(=)
Unknown
-
VUS
g.149539757A>G
-
TAB2(NM_001292035.3):c.-148-2A>G
-
TAB2_000060
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
?/.
-
c.-680C>T
r.(?)
p.(=)
Unknown
-
VUS
g.149639177C>T
-
TAB2(NM_001292034.3):c.-90+26C>T
-
TAB2_000069
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
?/.
-
c.-89-12623T>C
r.(=)
p.(=)
Both (homozygous)
-
VUS
g.149678422T>C
g.149357286T>C
-
-
TAB2_000004
-
-
-
-
Germline
-
-
-
-
-
DNA
SEQ-NG-I
-
-
CHTE
-
PubMed: Sun 2011
,
Journal: Sun 2011
-
M
no
Netherlands
-
-
-
-
-
1
Yu Sun
?/.
-
c.-89-12611C>G
r.(=)
p.(=)
Both (homozygous)
-
VUS
g.149678434C>G
g.149357298C>G
-
-
TAB2_000005
-
-
-
-
Germline
-
-
-
-
-
DNA
SEQ-NG-I
-
-
CHTE
-
PubMed: Sun 2011
,
Journal: Sun 2011
-
M
no
Netherlands
-
-
-
-
-
1
Yu Sun
-?/.
-
c.-89-12479A>C
r.(=)
p.(=)
Unknown
-
likely benign
g.149678566A>C
-
TAB2(NM_001292034.3):c.-89-12479A>C
-
TAB2_000070
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-?/.
-
c.-89-8_-89-5dup
r.spl?
p.?
Unknown
-
likely benign
g.149691037_149691040dup
-
TAB2(NM_015093.6):c.-89-8_-89-5dupTTTC
-
TAB2_000042
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
+/.
-
c.(-89-12805_103-3935)_*1892{0}
r.?
p.?
Maternal (confirmed)
-
pathogenic (dominant)
g.(149678240_149695219)_qterdelins[NC_000002.11:g.(131691033_131705253)_qter)]
-
-
t(2;6)(q21;q25)
TAB2_000046
-
PubMed: Thienpont 2010
-
-
Germline
yes
-
-
-
-
DNA
arrayCGH, FISH
-
-
CHTD
FamNPatIII2
PubMed: Thienpont 2010
4-generation family, 3 affected (mother, daughter/son); son
M
-
-
-
-
-
-
-
3
Johan den Dunnen
+/.
_1_9_
c.-421_*1892{0}
r.0
p.0
Maternal (confirmed)
-
pathogenic (dominant)
g.(?_149580983)_(149861981_?)del
-
-
-
TAB2_000045
281 kb deletion incl. TAB2, SUMO4, ZC3H12D, PPIL4; FISH RP1-144O21 deleted
PubMed: Weiss 2015
-
-
Germline
yes
-
-
-
-
DNA
arrayCGH
-
Infinium CytoSNP-850K beadchip
CHTD
FamPatIII1
PubMed: Weiss 2015
3-generation family, 3 affected (3F)
F
-
United States
-
-
-
-
-
3
Johan den Dunnen
+/.
_1_9_
c.-421_*1892{0}
r.0
p.0
Unknown
-
pathogenic (dominant)
g.(?_149580983)_(149861981_?)del
-
-
-
TAB2_000045
281 kb deletion incl. TAB2, SUMO4, ZC3H12D, PPIL4; FISH RP1-144O21 deleted
PubMed: Weiss 2015
-
-
Germline/De novo (untested)
yes
-
-
-
-
DNA
arrayCGH
-
Infinium CytoSNP-850K beadchip
CHTD
FamPatI1
PubMed: Weiss 2015
grandmother
F
-
United States
-
-
-
-
-
1
Johan den Dunnen
+/.
_1_9_
c.-421_*1892{0}
r.0
p.0
Maternal (confirmed)
-
pathogenic (dominant)
g.(?_149580983)_(149861981_?)del
-
-
-
TAB2_000045
281 kb deletion incl. TAB2, SUMO4, ZC3H12D, PPIL4; FISH RP1-144O21 deleted
PubMed: Weiss 2015
-
-
Germline
yes
-
-
-
-
DNA
arrayCGH
-
Infinium CytoSNP-850K beadchip
CHTD
FamPatII3
PubMed: Weiss 2015
mother
F
-
United States
-
-
-
-
-
1
Johan den Dunnen
?/.
-
c.25G>A
r.(?)
p.(Asp9Asn)
Unknown
-
VUS
g.149691158G>A
-
TAB2(NM_001369506.1):c.25G>A (p.D9N)
-
TAB2_000051
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-?/.
-
c.103-65A>G
r.(=)
p.(=)
Unknown
-
likely benign
g.149699089A>G
-
TAB2(NM_015093.6):c.103-65A>G
-
TAB2_000061
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-?/.
-
c.282A>G
r.(?)
p.(=)
Unknown
-
likely benign
g.149699333A>G
-
TAB2(NM_001292034.3):c.282A>G (p.(Gly94=))
-
TAB2_000071
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-?/.
-
c.353A>G
r.(?)
p.(Asn118Ser)
Unknown
-
likely benign
g.149699404A>G
-
TAB2(NM_015093.4):c.353A>G (p.(Asn118Ser))
-
TAB2_000063
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
+/.
-
c.446C>G
r.(?)
p.(Ser149*)
Maternal (confirmed)
ACMG
pathogenic (dominant)
g.149699497C>G
-
C446G
-
TAB2_000048
ACMG PVS1, PM2, PP1, PP3, PP4
PubMed: Chen 2020
-
-
Germline
yes
-
-
-
-
DNA
SEQ, SEQ-NG
-
WES
CHTD
FamPatII5
PubMed: Chen 2020
3-generation family, 8 affected (6F, M, fetus)
F
-
China
-
-
-
-
-
8
Johan den Dunnen
?/.
-
c.566G>A
r.(?)
p.(Arg189His)
Unknown
-
VUS
g.149699617G>A
-
TAB2(NM_015093.4):c.566G>A (p.(Arg189His))
-
TAB2_000064
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
+?/.
-
c.619dup
r.(?)
p.(Ser207LysfsTer10)
Unknown
-
likely pathogenic
g.149699670dup
g.149378534dup
-
-
TAB2_000019
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
+/.
-
c.619dup
r.(?)
p.(Ser207LysfsTer10)
Unknown
-
pathogenic (dominant)
g.149699670dup
g.149378534dup
-
-
TAB2_000019
linked to variant 610078 VKGL initiative
Journal: Engwerda 2021
-
-
De novo
-
-
-
-
-
DNA
SEQ-NG
-
WES
CHTD
PatA1
Journal: Engwerda 2021
2-generation family, 1 affected, unaffected heterozygous carrier parents
M
-
Netherlands
-
-
-
-
-
1
Aafke Engwerda
+/.
5
c.622C>T
r.(?)
p.(Pro208Ser)
Unknown
-
pathogenic (dominant)
g.149699673C>T
g.149378537C>T
-
-
TAB2_000001
-
PubMed: Thienpont 2010
-
-
Germline/De novo (untested)
-
-
-
-
-
DNA
SEQ
-
-
?
PatL
PubMed: Thienpont 2010
-
F
-
-
-
61y
-
-
-
1
LOVD
?/.
-
c.641A>G
r.(?)
p.(Tyr214Cys)
Unknown
-
VUS
g.149699692A>G
-
TAB2(NM_001292034.2):c.641A>G (p.(Tyr214Cys))
-
TAB2_000056
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
+/.
-
c.679C>T
r.(?)
p.(Arg227*)
Unknown
ACMG
pathogenic
g.149699730C>T
g.149378594C>T
-
-
TAB2_000044
-
-
VCV000561124.1
-
Germline
-
-
-
-
-
DNA
SEQ-NG-I
Blood
Clinical exome (4400 genes)
CHTD
patient
-
-
F
no
Finland
-
-
-
-
-
1
Maria K Haanpää
+?/.
-
c.682C>T
r.(?)
p.(Gln228Ter)
Unknown
-
likely pathogenic
g.149699733C>T
g.149378597C>T
-
-
TAB2_000020
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
+/.
-
c.682C>T
r.(?)
p.(Gln228Ter)
Unknown
-
pathogenic (dominant)
g.149699733C>T
g.149378597C>T
-
-
TAB2_000020
linked to variant 610079 VKGL initiative; variant not maternal
Journal: Engwerda 2021
-
-
Germline/De novo (untested)
-
-
-
-
-
DNA
SEQ-NG
-
WES
CHTD
PatB1
Journal: Engwerda 2021
2-generation family, 1 affected, unaffected parents
M
-
Netherlands
-
-
-
-
-
1
Aafke Engwerda
+/.
-
c.688C>A
r.(?)
p.(Gln230Lys)
Unknown
-
pathogenic (dominant)
g.149699739C>A
g.149378603C>A
-
-
TAB2_000002
-
PubMed: Thienpont 2010
-
-
Germline/De novo (untested)
-
-
-
-
-
DNA
SEQ
-
-
?
PatM
PubMed: Thienpont 2010
-
M
-
-
-
-
-
-
-
1
LOVD
-?/.
-
c.725T>G
r.(?)
p.(Met242Arg)
Unknown
-
likely benign
g.149699776T>G
-
TAB2(NM_001292034.3):c.725T>G (p.(Met242Arg))
-
TAB2_000068
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
?/.
-
c.725T>G
r.(?)
p.(Met242Arg)
Unknown
-
VUS
g.149699776T>G
-
TAB2(NM_001292034.3):c.725T>G (p.(Met242Arg))
-
TAB2_000068
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
+/.
4
c.731del
r.(?)
p.(Pro244Leufs*117)
Unknown
ACMG
pathogenic (dominant)
g.149699782del
g.149378646del
731delC
-
TAB2_000038
-
-
-
-
Germline
yes
-
-
-
-
DNA
SEQ-NG-I
-
-
CHD
I2
-
-
M
no
Italy
-
-
-
-
-
1
Lucia Micale
+?/.
-
c.733C>T
r.(?)
p.(Gln245Ter)
Unknown
-
likely pathogenic
g.149699784C>T
g.149378648C>T
TAB2(NM_015093.4):c.733C>T (p.(Gln245Ter))
-
TAB2_000026
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-?/.
-
c.774T>C
r.(?)
p.(Thr258=)
Unknown
-
likely benign
g.149699825T>C
g.149378689T>C
-
-
TAB2_000021
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-?/.
-
c.809C>G
r.(?)
p.(Ser270Cys)
Unknown
-
likely benign
g.149699860C>G
-
TAB2(NM_015093.4):c.809C>G (p.(Ser270Cys))
-
TAB2_000065
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
?/.
-
c.853A>C
r.(?)
p.(Met285Leu)
Unknown
-
VUS
g.149699904A>C
g.149378768A>C
TAB2(NM_015093.6):c.853A>C (p.M285L)
-
TAB2_000013
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
?/.
-
c.859A>G
r.(?)
p.(Ile287Val)
Unknown
-
VUS
g.149699910A>G
-
TAB2(NM_001292034.3):c.859A>G (p.(Ile287Val)), TAB2(NM_015093.5):c.859A>G (p.I287V)
-
TAB2_000032
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
?/.
-
c.859A>G
r.(?)
p.(Ile287Val)
Unknown
-
VUS
g.149699910A>G
-
TAB2(NM_001292034.3):c.859A>G (p.(Ile287Val)), TAB2(NM_015093.5):c.859A>G (p.I287V)
-
TAB2_000032
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
+/.
-
c.872_873del
r.(?)
p.(Thr291Asnfs*12)
Unknown
-
pathogenic
g.149699923_149699924del
g.149378787_149378788del
-
-
TAB2_000031
-
-
-
-
Unknown
-
-
-
-
-
DNA
SEQ
-
-
?
-
-
-
F
-
-
-
-
-
-
-
1
IMGAG
+/.
-
c.885_886del
r.(?)
p.(Pro296AsnfsTer7)
Unknown
-
pathogenic
g.149699936_149699937del
-
TAB2(NM_015093.6):c.885_886delAC (p.P296Nfs*7)
-
TAB2_000009
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
+/.
-
c.885_886del
r.(?)
p.(Pro296AsnfsTer7)
Unknown
-
pathogenic (dominant)
g.149699936_149699937del
g.149378800_149378801del
-
-
TAB2_000009
linked to variant 720715 VKGL initiative
Journal: Engwerda 2021
-
-
Germline/De novo (untested)
-
-
-
-
-
DNA
SEQ
-
-
CHTD
PatC1
Journal: Engwerda 2021
2-generation family, 3 affected (2F, M), unaffected heterozygous carrier parents
F
-
Netherlands
-
-
-
-
-
3
Aafke Engwerda
+/.
-
c.885_886del
r.(?)
p.(Pro296AsnfsTer7)
Maternal (confirmed)
-
pathogenic (dominant)
g.149699936_149699937del
g.149378800_149378801del
-
-
TAB2_000009
linked to variant 720715 VKGL initiative
Journal: Engwerda 2021
-
-
Germline
-
-
-
-
-
DNA
SEQ
-
-
CHTD
PatC2
Journal: Engwerda 2021
son
M
-
Netherlands
-
-
-
-
-
1
Aafke Engwerda
+/.
-
c.885_886del
r.(?)
p.(Pro296AsnfsTer7)
Maternal (confirmed)
-
pathogenic (dominant)
g.149699936_149699937del
g.149378800_149378801del
-
-
TAB2_000009
linked to variant 720715 VKGL initiative
Journal: Engwerda 2021
-
-
Germline
-
-
-
-
-
DNA
SEQ
-
-
CHTD
PatC3
Journal: Engwerda 2021
daughter
F
-
Netherlands
-
-
-
-
-
1
Aafke Engwerda
+/.
4
c.889A>G
r.(?)
p.(Thr297Ala)
Unknown
ACMG
pathogenic (dominant)
g.149699940A>G
-
-
-
TAB2_000039
-
-
-
-
Germline
yes
-
-
-
-
DNA
SEQ-NG-I
-
-
CHD
IIII
-
-
F
no
Italy
-
-
-
-
-
1
Lucia Micale
+/.
-
c.899C>A
r.(?)
p.(Ser300Ter)
Unknown
-
pathogenic
g.149699950C>A
g.149378814C>A
TAB2(NM_015093.6):c.899C>A (p.S300*)
-
TAB2_000010
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
+/.
-
c.899C>A
r.(?)
p.(Ser300Ter)
Unknown
-
pathogenic
g.149699950C>A
-
TAB2(NM_015093.6):c.899C>A (p.S300*)
-
TAB2_000010
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
+/.
-
c.899C>A
r.(?)
p.(Ser300Ter)
Unknown
-
pathogenic (dominant)
g.149699950C>A
g.149378814C>A
-
-
TAB2_000010
linked to variants 348920/720716 (same family) VKGL initiative
Journal: Engwerda 2021
-
-
Germline/De novo (untested)
-
-
-
-
-
DNA
SEQ
-
-
CHTD
PatD1
Journal: Engwerda 2021
family, 6 affected (4F, 2M), unaffected heterozygous carrier parents
F
-
Netherlands
-
46y
-
-
-
6
Aafke Engwerda
+/.
-
c.899C>A
r.(?)
p.(Ser300Ter)
Maternal (confirmed)
-
pathogenic (dominant)
g.149699950C>A
g.149378814C>A
-
-
TAB2_000010
linked to variants 348920/720716 (same family) VKGL initiative
Journal: Engwerda 2021
-
-
Germline
-
-
-
-
-
DNA
SEQ
-
-
CHTD
PatD2
Journal: Engwerda 2021
-
M
-
Netherlands
-
-
-
-
-
1
Aafke Engwerda
+/.
-
c.899C>A
r.(?)
p.(Ser300Ter)
Maternal (confirmed)
-
pathogenic (dominant)
g.149699950C>A
g.149378814C>A
-
-
TAB2_000010
linked to variants 348920/720716 (same family) VKGL initiative
Journal: Engwerda 2021
-
-
Germline
-
-
-
-
-
DNA
SEQ
-
-
CHTD
PatD3
Journal: Engwerda 2021
-
F
-
Netherlands
-
-
-
-
-
1
Aafke Engwerda
+/.
-
c.899C>A
r.(?)
p.(Ser300Ter)
Paternal (confirmed)
-
pathogenic (dominant)
g.149699950C>A
g.149378814C>A
-
-
TAB2_000010
linked to variants 348920/720716 (same family) VKGL initiative
Journal: Engwerda 2021
-
-
Germline
-
-
-
-
-
DNA
SEQ
-
-
CHTD
PatD4
Journal: Engwerda 2021
-
F
-
Netherlands
-
-
-
-
-
1
Aafke Engwerda
+/.
-
c.899C>A
r.(?)
p.(Ser300Ter)
Paternal (confirmed)
-
pathogenic (dominant)
g.149699950C>A
g.149378814C>A
-
-
TAB2_000010
linked to variants 348920/720716 (same family) VKGL initiative
Journal: Engwerda 2021
-
-
Germline
-
-
-
-
-
DNA
SEQ
-
-
CHTD
PatD5
Journal: Engwerda 2021
-
F
-
Netherlands
-
-
-
-
-
1
Aafke Engwerda
+/.
-
c.899C>A
r.(?)
p.(Ser300Ter)
Maternal (confirmed)
-
pathogenic (dominant)
g.149699950C>A
g.149378814C>A
-
-
TAB2_000010
linked to variants 348920/720716 (same family) VKGL initiative
Journal: Engwerda 2021
-
-
Germline
-
-
-
-
-
DNA
SEQ-NG
-
WES
CHTD
PatD6
Journal: Engwerda 2021
-
M
-
Netherlands
-
-
-
-
-
1
Aafke Engwerda
?/.
-
c.972C>A
r.(?)
p.(Asn324Lys)
Unknown
-
VUS
g.149700023C>A
-
TAB2(NM_015093.6):c.972C>A (p.N324K)
-
TAB2_000052
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-?/.
-
c.1077C>T
r.(?)
p.(Thr359=)
Unknown
-
likely benign
g.149700128C>T
g.149378992C>T
TAB2(NM_015093.5):c.1077C>T (p.T359=)
-
TAB2_000027
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
?/.
-
c.1121dup
r.(?)
p.(Asn375LysfsTer4)
Unknown
-
VUS
g.149700172dup
g.149379036dup
TAB2(NM_015093.4):c.1121dup (p.(Asn375LysfsTer4))
-
TAB2_000014
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
?/.
-
c.1123A>G
r.(?)
p.(Asn375Asp)
Unknown
-
VUS
g.149700174A>G
-
TAB2(NM_015093.6):c.1123A>G (p.N375D)
-
TAB2_000057
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
?/.
-
c.1127C>T
r.(?)
p.(Thr376Met)
Unknown
-
VUS
g.149700178C>T
g.149379042C>T
TAB2(NM_015093.5):c.1127C>T (p.T376M)
-
TAB2_000028
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-/.
-
c.1128G>A
r.(?)
p.(Thr376=)
Unknown
-
benign
g.149700179G>A
g.149379043G>A
TAB2(NM_001292034.3):c.1128G>A (p.(Thr376=)), TAB2(NM_015093.5):c.1128G>A (p.T376=)
-
TAB2_000015
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-?/.
-
c.1128G>A
r.(?)
p.(Thr376=)
Unknown
-
likely benign
g.149700179G>A
g.149379043G>A
TAB2(NM_001292034.3):c.1128G>A (p.(Thr376=)), TAB2(NM_015093.5):c.1128G>A (p.T376=)
-
TAB2_000015
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-?/.
-
c.1128G>A
r.(?)
p.(Thr376=)
Unknown
-
likely benign
g.149700179G>A
-
TAB2(NM_001292034.3):c.1128G>A (p.(Thr376=)), TAB2(NM_015093.5):c.1128G>A (p.T376=)
-
TAB2_000015
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-?/.
-
c.1155T>C
r.(?)
p.(Pro385=)
Unknown
-
likely benign
g.149700206T>C
g.149379070T>C
TAB2(NM_015093.5):c.1155T>C (p.P385=)
-
TAB2_000029
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
?/.
-
c.1192G>A
r.(?)
p.(Glu398Lys)
Unknown
-
VUS
g.149700243G>A
-
TAB2(NM_015093.5):c.1192G>A (p.E398K)
-
TAB2_000049
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
+/.
-
c.1227dup
r.(?)
p.(Ser410Ilefs*37)
Unknown
-
pathogenic
g.149700278dup
-
TAB2(NM_015093.6):c.1227dupA (p.S410Ifs*37)
-
SUMO4_000005
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
+/.
-
c.1227dup
r.(?)
p.(Ser410IlefsTer37)
Unknown
-
pathogenic (dominant)
g.149700278dup
g.149379142dup
-
-
SUMO4_000005
linked to variant 720717 VKGL initiative (c.1227dup)
Journal: Engwerda 2021
-
-
De novo
-
-
-
-
-
DNA
SEQ-NG
-
WES
CHTD
PatE1
Journal: Engwerda 2021
2-generation family, affected mother/son, unaffected heterozygous carrier parents
F
-
Netherlands
-
-
-
-
-
2
Aafke Engwerda
+/.
-
c.1227dup
r.(?)
p.(Ser410IlefsTer37)
Maternal (confirmed)
-
pathogenic (dominant)
g.149700278dup
g.149379142dup
-
-
SUMO4_000005
linked to variant 720717 VKGL initiative (c.1227dup)
Journal: Engwerda 2021
-
-
Germline
-
-
-
-
-
DNA
SEQ
-
-
CHTD
PatE2
Journal: Engwerda 2021
son
M
-
Netherlands
-
-
-
-
-
1
Aafke Engwerda
+/.
-
c.1321C>T
r.(?)
p.(Arg441*)
Unknown
ACMG
likely pathogenic (dominant)
g.149700372C>T
g.149379236C>T
-
-
TAB2_000037
-
-
-
-
De novo
-
-
-
-
-
DNA
SEQ-NG-I
blood
WES
cutis laxa
-
-
-
F
no
-
-
-
-
-
-
1
Bert Callewaert
+/.
-
c.1340_1341del
r.(?)
p.(Ser447CysfsTer25)
Unknown
-
pathogenic
g.149700391_149700392del
-
TAB2(NM_015093.5):c.1340_1341delCT (p.S447Cfs*25), TAB2(NM_015093.6):c.1340_1341delCT (p.S447Cfs*25)
-
TAB2_000016
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
+/.
-
c.1340_1341del
r.(?)
p.(Ser447CysfsTer25)
Unknown
-
pathogenic
g.149700391_149700392del
-
TAB2(NM_015093.5):c.1340_1341delCT (p.S447Cfs*25), TAB2(NM_015093.6):c.1340_1341delCT (p.S447Cfs*25)
-
TAB2_000016
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
+?/.
-
c.1354C>T
r.(?)
p.(Arg452Ter)
Unknown
-
likely pathogenic
g.149700405C>T
g.149379269C>T
TAB2(NM_015093.6):c.1354C>T (p.R452*)
-
TAB2_000008
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
+?/.
-
c.1354C>T
r.(?)
p.(Arg452*)
Unknown
-
pathogenic (dominant)
g.149700405C>T
g.149379269C>T
-
-
TAB2_000008
-
-
-
-
Germline
?
-
-
-
-
DNA
SEQ-NG
-
-
CHTD2
-
-
-
M
no
Belgium
whitet
-
-
-
-
1
Jeroen Breckpot
+?/.
-
c.1385dup
r.(?)
p.(Tyr462*)
Unknown
ACMG
pathogenic (dominant)
g.149700436dup
g.149379300dup
-
-
TAB2_000040
-
-
-
-
Germline/De novo (untested)
yes
-
-
-
-
DNA
SEQ-NG-I
-
-
CHTD2
P I8
-
-
F
no
(Switzerland)
central european, white
>05y
-
-
-
1
Cecilia Giunta
+/.
-
c.1398dup
r.1398dup
p.Thr467Tyrfs*6
Unknown
-
pathogenic
g.149700449dup
g.149379313dup
-
-
TAB2_000012
nonsense-mediated mRNA decay; truncated protein loses ability to bind TAK1, alteration TAK1 autophosphorylation status; patient fibroblasts display ECM disorganization and altered expression of selected ECM components and collagen-related pathways
PubMed: Morlino 2019
,
PubMed: Ritelli 2018
-
-
Germline
-
-
-
-
-
DNA
SEQ-NG
peripheral blood
-
?
-
PubMed: Morlino 2019
,
PubMed: Ritelli 2018
2-generation family, 3 affected individuals
F
no
Italy
white
-
-
-
-
3
Lucia Micale
+/.
-
c.1398dup
r.(?)
p.(Thr467Tyrfs*6)
Paternal (inferred)
-
pathogenic (dominant)
g.149700449dup
g.149379313dup
-
-
TAB2_000012
-
PubMed: Ritelli 2018
-
-
Germline
yes
-
-
-
-
DNA
SEQ, SEQ-NG
-
WES
CHTD
Fam1Pat1
PubMed: Ritelli 2018
3-generation family, 3 affected (2F, M)
F
-
Italy
-
-
-
-
-
3
Johan den Dunnen
+/.
-
c.1398dup
r.(?)
p.(Thr467Tyrfs*6)
Unknown
-
pathogenic (dominant)
g.149700449dup
g.149379313dup
-
-
TAB2_000012
-
PubMed: Ritelli 2018
-
-
Germline
yes
-
-
-
-
DNA
SEQ, SEQ-NG
-
WES
CHTD
Fam1Pat2
PubMed: Ritelli 2018
-
F
-
Italy
-
-
-
-
-
1
Johan den Dunnen
+/.
-
c.1398dup
r.(?)
p.(Thr467Tyrfs*6)
Unknown
-
pathogenic (dominant)
g.149700449dup
g.149379313dup
-
-
TAB2_000012
-
PubMed: Ritelli 2018
-
-
Germline
yes
-
-
-
-
DNA
SEQ, SEQ-NG
-
WES
CHTD
Fam1Pat3
PubMed: Ritelli 2018
-
M
-
Italy
-
-
-
-
-
1
Johan den Dunnen
+/.
-
c.1491T>A
r.(?)
p.(Tyr497*)
Unknown
ACMG
pathogenic (dominant)
g.149700542T>A
g.149379406T>A
-
-
TAB2_000047
ACMG PVS1, PS2, PS3
PubMed: Ackerman 2016
-
-
De novo
-
-
-
-
-
DNA
SEQ, SEQ-NG
-
trio WES
CHTD
patient
PubMed: Ackerman 2016
2-generation family, 1 affected, unaffected non-carrier parents
M
no
United States
-
-
-
-
-
1
Johan den Dunnen
-?/.
-
c.1501G>A
r.(?)
p.(Glu501Lys)
Unknown
-
likely benign
g.149700552G>A
-
TAB2(NM_001292034.3):c.1501G>A (p.(Glu501Lys))
-
TAB2_000073
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
+?/.
-
c.1510C>T
r.(?)
p.(Gln504*)
Unknown
ACMG
pathogenic (dominant)
g.149700561C>T
g.149379425C>T
g.14969973C>T
-
TAB2_000036
-
-
-
-
Germline/De novo (untested)
yes
-
-
-
-
DNA
SEQ-NG-I
-
-
CHTD2
P I9
-
-
F
no
Switzerland
central european, white
>13y
-
-
-
1
Cecilia Giunta
+?/.
4
c.1516del
r.(?)
p.(Leu506Serfs*6)
Unknown
ACMG
pathogenic
g.149700567del
g.149379431del
1516delC
-
TAB2_000041
-
-
-
-
Germline
yes
-
-
-
-
DNA
SEQ-NG-I
-
-
CHD
I10
-
-
-
-
Italy
-
-
-
-
-
1
Lucia Micale
-?/.
-
c.1537C>G
r.(?)
p.(His513Asp)
Unknown
-
likely benign
g.149700588C>G
-
TAB2(NM_015093.4):c.1537C>G (p.(His513Asp))
-
TAB2_000066
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-?/.
-
c.1603+7T>C
r.(=)
p.(=)
Unknown
-
likely benign
g.149700661T>C
g.149379525T>C
-
-
TAB2_000017
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
+/.
-
c.1619A>G
r.(?)
p.(Gln540Arg)
Unknown
-
pathogenic
g.149718755A>G
g.149397619A>G
-
-
TAB2_000011
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
+?/.
6
c.1636C>T
r.(1636c>u)
p.(Arg546Ter)
Maternal (confirmed)
-
pathogenic
g.149718772C>T
g.149397636C>T
-
-
TAB2_000030
-
PubMed: Liu 2020
,
Journal: Liu 2020
-
-
Germline
yes
1/80 patients
-
-
-
DNA
SEQ, SEQ-NG-I
Thymus
-
CHD, HLHS1
Pt5521
PubMed: Liu 2020
,
Journal: Liu 2020
-
F
no
France
-
00y
-
-
-
4
Patrice Bouvagnet
+?/.
6
c.1636C>T
r.(1636c>u)
p.(Arg546Ter)
Unknown
-
pathogenic
g.149718772C>T
g.149397636C>T
-
-
TAB2_000030
-
PubMed: Liu 2020
,
Journal: Liu 2020
-
-
De novo
yes
-
-
-
-
DNA
SEQ
Blood
-
ASD
Pt5519
PubMed: Liu 2020
,
Journal: Liu 2020
-
F
no
France
-
>42y
-
-
-
2
Patrice Bouvagnet
+?/.
6
c.1636C>T
r.(1636c>u)
p.(Arg546Ter)
Maternal (confirmed)
-
pathogenic
g.149718772C>T
g.149397636C>T
-
-
TAB2_000030
-
PubMed: Liu 2020
,
Journal: Liu 2020
-
-
Germline
yes
-
-
-
-
DNA
SEQ
Blood
-
ASD
Pt5518
PubMed: Liu 2020
,
Journal: Liu 2020
-
F
no
France
-
>18y
-
-
-
3
Patrice Bouvagnet
+?/.
6
c.1636C>T
r.(1636c>u)
p.(Arg546Ter)
Maternal (confirmed)
-
pathogenic
g.149718772C>T
g.149397636C>T
-
-
TAB2_000030
-
PubMed: Liu 2020
,
Journal: Liu 2020
-
-
Germline
yes
-
-
-
-
DNA
SEQ
Blood
-
ASD1
Pt5519
PubMed: Liu 2020
,
Journal: Liu 2020
-
F
no
France
-
>16y
-
-
-
3
Patrice Bouvagnet
+/.
-
c.1636C>T
r.(?)
p.(Arg546*)
Unknown
-
pathogenic
g.149718772C>T
-
-
-
TAB2_000030
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-?/.
-
c.1644A>G
r.(?)
p.(Gln548=)
Unknown
-
likely benign
g.149718780A>G
g.149397644A>G
-
-
TAB2_000022
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
+/?
-
c.1705G>A
r.(?)
p.(Glu569Lys)
Parent #1
-
pathogenic
g.149718841G>A
g.149397705G>A
-
-
TAB2_000007
curator: variant classified as VUS because its contribution to frontometaphyseal dysplasia has not been confirmed
PubMed: Wade 2016
,
Journal: Wade 2016
-
-
De novo
-
-
-
-
-
DNA, RNA
PCRq, SEQ, SEQ-NG-I, Western
-
-
FMD1
27426733-Pat17
PubMed: Wade 2016
,
Journal: Wade 2016
-
F
-
Australia
European
-
-
-
-
1
Jamie Zeegers
?/.
-
c.1727G>A
r.(?)
p.(Arg576His)
Unknown
-
VUS
g.149718863G>A
g.149397727G>A
TAB2(NM_015093.4):c.1727G>A (p.(Arg576His))
-
TAB2_000023
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
?/.
-
c.1739C>T
r.(?)
p.(Ser580Leu)
Unknown
-
VUS
g.149718875C>T
-
TAB2(NM_015093.5):c.1739C>T (p.S580L)
-
TAB2_000050
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-?/.
-
c.1764C>T
r.(?)
p.(=)
Unknown
-
likely benign
g.149718900C>T
-
TAB2(NM_015093.6):c.1764C>T (p.S588=)
-
TAB2_000059
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-?/.
-
c.1765-3C>T
r.spl?
p.?
Unknown
-
likely benign
g.149719102C>T
-
TAB2(NM_015093.5):c.1765-3C>T
-
TAB2_000043
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
+?/.
-
c.1855C>T
r.(?)
p.(Arg619Ter)
Unknown
-
likely pathogenic
g.149719195C>T
g.149398059C>T
-
-
TAB2_000024
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
+/.
-
c.1855C>T
r.(?)
p.(Arg619Ter)
Unknown
-
pathogenic (dominant)
g.149719195C>T
g.149398059C>T
-
-
TAB2_000024
linked to variant 610084 VKGL initiative
Journal: Engwerda 2021
-
-
De novo
-
-
-
-
-
DNA
SEQ-NG
-
WES
CHTD
PatF1
Journal: Engwerda 2021
2-generation family, 1 affected, unaffected heterozygous carrier parents
F
-
Netherlands
-
-
-
-
-
1
Aafke Engwerda
?/.
-
c.1883T>A
r.(?)
p.(Ile628Asn)
Unknown
-
VUS
g.149720264T>A
-
TAB2(NM_015093.4):c.1883T>A (p.(Ile628Asn))
-
TAB2_000067
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-?/.
-
c.1926A>T
r.(?)
p.(Pro642=)
Unknown
-
likely benign
g.149720307A>T
-
TAB2(NM_015093.6):c.1926A>T (p.P642=)
-
TAB2_000053
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-?/.
-
c.1939+278T>C
r.(=)
p.(=)
Unknown
-
likely benign
g.149720598T>C
-
TAB2(NM_015093.6):c.1939+278T>C
-
TAB2_000058
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-?/.
-
c.1939+1209T>C
r.(=)
p.(=)
Unknown
-
likely benign
g.149721529T>C
-
SUMO4(NM_001002255.2):c.2T>C (p.(Met1?))
-
TAB2_000072
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-?/.
-
c.1939+1234A>C
r.(=)
p.(=)
Unknown
-
likely benign
g.149721554A>C
-
SUMO4(NM_001002255.2):c.27A>C (p.(Glu9Asp))
-
TAB2_000062
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
?/.
-
c.1939+1370G>A
r.(=)
p.(=)
Both (homozygous)
-
VUS
g.149721690G>A
g.149400554G>A
-
-
SUMO4_000002
-
-
-
-
Germline
-
-
-
-
-
DNA
SEQ-NG-I
-
-
CHTE
-
PubMed: Sun 2011
,
Journal: Sun 2011
-
M
no
Netherlands
-
-
-
-
-
1
Yu Sun
?/.
-
c.1939+1370G>A
r.(=)
p.(=)
Both (homozygous)
-
VUS
g.149721690G>A
g.149400554G>A
-
-
SUMO4_000002
-
-
-
-
Germline
-
-
-
-
-
DNA
SEQ-NG-I
-
-
CHTE
-
PubMed: Sun 2011
,
Journal: Sun 2011
-
M
no
Netherlands
-
-
-
-
-
1
Yu Sun
-/.
-
c.1939+1370G>A
r.(=)
p.(=)
Unknown
-
benign
g.149721690G>A
g.149400554G>A
SUMO4(NM_001002255.2):c.163G>A (p.V55M), TAB2(NM_015093.5):c.1939+1370G>A
-
SUMO4_000002
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-/.
-
c.1939+1370G>A
r.(=)
p.(=)
Unknown
-
benign
g.149721690G>A
-
SUMO4(NM_001002255.2):c.163G>A (p.V55M), TAB2(NM_015093.5):c.1939+1370G>A
-
SUMO4_000002
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
-
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