Global Variome shared LOVD
ALDOB (aldolase B, fructose-bisphosphate)
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Unique variants in the ALDOB gene
The variants shown are described using the NM_000035.3 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.
Reported
: The number of times this variant has been reported in the database.
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
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%)
How to query this table
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Operator
Column type
Example
Matches
Text
Arg
all entries containing 'Arg'
space
Text
Arg Ser
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|
Text
Arg|Ser
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!
Text
!fs
all entries not containing 'fs'
^
Text
^p.(Arg
all entries beginning with 'p.(Arg'
$
Text
Ser)$
all entries ending with 'Ser)'
=""
Text
=""
all entries with this field empty
=""
Text
="p.0"
all entries exactly matching 'p.0'
!=""
Text
!=""
all entries with this field not empty
!=""
Text
!="p.0"
all entries not exactly matching 'p.0?'
combination
Text
*|Ter !fs
all entries containing '*' or 'Ter' but not containing 'fs'
Date
2020
all entries matching the year 2020
|
Date
2020-03|2020-04
all entries matching March or April, 2020
!
Date
!2020-03
all entries not matching March, 2020
<
Date
<2020
all entries before the year 2020
<=
Date
<=2020-06
all entries in or before June, 2020
>
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
all entries in 2019 or 2020, and before March, 2020
Numeric
23
all entries exactly matching 23
|
Numeric
23|24
all entries exactly matching 23 or 24
!
Numeric
!23
all entries not exactly matching 23
<
Numeric
<23
all entries lower than 23
<=
Numeric
<=23
all entries lower than, or equal to, 23
>
Numeric
>23
all entries higher than 23
>=
Numeric
>=23
all entries higher than, or equal to, 23
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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Legend
How to query
Effect
Reported
Exon
DNA change (cDNA)
RNA change
Protein
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
Owner
+?/.
2
_1
-
r.(=)
p.(=)
-
likely pathogenic (recessive)
g.104198184C>T
g.101435902C>T
g.-132G>A
-
ALDOB_000070
in vitro expression cloning decreased transcription using luciferase reporter plasmids,
1 more item
PubMed: Coffee 2010
-
-
Germline
-
g.-132G>A
-
-
-
Johan den Dunnen
?/.
1
-
c.-214G>A
r.(?)
p.(=)
-
VUS
g.104198194C>T
-
-
-
ALDOB_000076
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Nijmegen
-/.
1
-
c.-211T>A
r.(?)
p.(=)
-
benign
g.104198191A>T
-
-
-
ALDOB_000071
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Nijmegen
+/.
5
1i_6i
c.-10-2043_624+63del
r.?
p.0?
-
pathogenic (recessive)
g.104188775_104195223del
g.101426493_101432941del
g.2840_9288del
-
ALDOB_000036
6,548 bp deletion, unknown variant 2nd chromosome
PubMed: Esposito 2010
-
-
Germline
-
6/244 chromosomes (cases)
-
-
-
Johan den Dunnen
-?/.
1
-
c.-10-17C>T
r.(=)
p.(=)
-
likely benign
g.104193196G>A
-
ALDOB(NM_000035.4):c.-10-17C>T
-
ALDOB_000073
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Utrecht
+/.
4
1i
c.-10-1G>C
r.?
p.?
-
pathogenic (recessive)
g.104193180C>G
g.101430898C>G
-
-
ALDOB_000069
unknown variant 2nd chromosome
PubMed: Coffee 2010
-
-
Germline
-
-
-
-
-
Johan den Dunnen
+/.
1
2
c.2T>C
r.(?)
p.(Met1?)
-
pathogenic (recessive)
g.104193168A>G
g.101430886A>G
M1T
-
ALDOB_000068
-
PubMed: Ali 1993
-
-
Germline
-
-
-
-
-
Johan den Dunnen
+/., +?/.
2
2
c.10C>T
r.(?)
p.(Arg4*)
-
likely pathogenic, pathogenic (recessive)
g.104193160G>A
g.101430878G>A
-
-
ALDOB_000014
1 heterozygous, no homozygous;
Clinindb (India)
PubMed: Ali 1994
,
PubMed: Narang 2020
,
Journal: Narang 2020
-
rs118204428
Germline
-
1/2795 individuals
-
-
-
Johan den Dunnen
,
Mohammed Faruq
+/.
3
2
c.62del
r.(?)
p.(Gln21Argfs*17)
-
pathogenic (recessive)
g.104193108del
g.101430826del
AA20delA
-
ALDOB_000067
unknown variant 2nd chromosome
PubMed: Esposito 2010
,
PubMed: Santamaria 1996
-
-
Germline
-
1/244 chromosomes (cases)
-
-
-
Johan den Dunnen
+/.
1
2i
c.112+1G>A
r.spl
p.?
-
pathogenic (recessive)
g.104193057C>T
g.101430775C>T
-
-
ALDOB_000066
-
PubMed: Davit-Spraul 2008
-
-
Germline
-
1/92 cases
-
-
-
Johan den Dunnen
+/.
1
2i
c.113-1G>A
r.spl
p.?
-
pathogenic (recessive)
g.104192249C>T
g.101429967C>T
IVS2-1G>A
-
ALDOB_000065
unknown variant 2nd chromosome
PubMed: Santer 2005
-
-
Germline
-
1/144 chromosomes cases
-
-
-
Johan den Dunnen
+/.
5
2i
c.113-1_115del
r.spl
p.?
-
pathogenic (recessive)
g.104192248_104192251del
g.101429966_101429969del
113-1_115delGGTA, del4, g922_925delgGTA
-
ALDOB_000064
-
PubMed: Ali 1995
,
PubMed: Cross 1990
,
PubMed: Gruchota 2006
-
-
Germline
-
1/52 chromosomes cases
-
-
-
Johan den Dunnen
+/.
1
3
c.136A>T
r.(?)
p.(Arg46Trp)
-
pathogenic (recessive)
g.104192225T>A
g.101429943T>A
-
-
ALDOB_000063
unknown variant 2nd chromosome
PubMed: Esposito 2010
-
-
Germline
-
1/244 chromosomes (cases)
-
-
-
Johan den Dunnen
+/.
1
3
c.146del
r.(?)
p.(Val49Glyfs*29)
-
pathogenic (recessive)
g.104192215del
g.101429933del
146delT
-
ALDOB_000062
-
PubMed: Davit-Spraul 2008
-
-
Germline
-
1/92 cases
-
-
-
Johan den Dunnen
-/.
1
-
c.156T>G
r.(?)
p.(Thr52=)
-
benign
g.104192205A>C
g.101429923A>C
ALDOB(NM_000035.4):c.156T>G (p.T52=)
-
ALDOB_000011
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Rotterdam
+/.
1
3
c.170G>C
r.(?)
p.(Arg57Pro)
-
pathogenic (recessive)
g.104192191C>G
g.101429909C>G
-
-
ALDOB_000061
-
PubMed: Davit-Spraul 2008
-
-
Germline
-
1/92 cases
-
-
-
Johan den Dunnen
+/.
7
3
c.178C>T
r.(?)
p.(Arg60*)
-
pathogenic, pathogenic (recessive)
g.104192183G>A
g.101429901G>A
R59X
-
ALDOB_000060
unknown variant 2nd chromosome, VKGL data sharing initiative Nederland
PubMed: Ali 1994
,
PubMed: Brooks 1994
,
PubMed: Coffee 2010
,
PubMed: Davit-Spraul 2008
,
1 more item
-
-
CLASSIFICATION record, Germline
-
2/144 chromosomes cases, 2/92 cases
-
-
-
Johan den Dunnen
,
VKGL-NL_Nijmegen
+/.
1
3
c.221T>C
r.(?)
p.(Ile74Thr)
-
pathogenic (recessive)
g.104192140A>G
g.101429858A>G
g.6846T>C
-
ALDOB_000059
-
PubMed: Esposito 2004
,
PubMed: Esposito 2010
-
-
Germline
-
1/244 chromosomes (cases)
-
-
-
Johan den Dunnen
+/.
2
3
c.250del
r.(?)
p.(Leu84Serfs*26)
-
pathogenic (recessive)
g.104192113del
g.101429831del
250delC
-
ALDOB_000058
-
PubMed: Gruchota 2006
-
-
Germline
-
2/52 chromosomes cases
-
-
-
Johan den Dunnen
+/.
1
-
c.264C>A
r.(?)
p.(Asp88Glu)
-
pathogenic
g.104192097G>T
g.101429815G>T
-
-
ALDOB_000077
variants reported seperately, unknown if mono-allelic or bi-allelic
PubMed: Retterer 2016
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
+/.
2
3
c.306_317dup
r.(?)
p.(Val104_Ile107dup)
-
pathogenic (recessive)
g.104192047_104192058dup
g.101429765_101429776dup
314-315ins12, 314_315insGGGGATCGTGGT
-
ALDOB_000057
unknown variant 2nd chromosome
PubMed: Esposito 2010
,
PubMed: Gruchota 2006
-
-
Germline
-
1/244 chromosomes (cases), 1/52 chromosomes cases
-
-
-
Johan den Dunnen
+/.
2
3
c.324G>A
r.313_324del, r.spl
p.(Val105_Lys108del), p.Val105_Lys108del
-
pathogenic (recessive)
g.104192037C>T
g.101429755C>T
g.1133G>A
-
ALDOB_000056
unknown variant 2nd chromosome
PubMed: Davit-Spraul 2008
,
PubMed: Sanchez-Gutierrez 2002
-
-
Germline
-
1/42 chromosomes cases, 1/92 cases
-
-
-
Johan den Dunnen
+/.
1
5
c.324+568_480del
r.(?)
p.?
-
pathogenic (recessive)
g.104189826_104191471del
g.101427544_101429189del
g.6594-8239del
-
ALDOB_000048
1646 bp deletion from IVS3 to part of E5
PubMed: Cross 1990
-
-
Germline
-
-
-
-
-
Johan den Dunnen
-?/.
1
-
c.325-19T>G
r.(=)
p.(=)
-
likely benign
g.104190824A>C
-
ALDOB(NM_000035.4):c.325-19T>G
-
ALDOB_000075
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Utrecht
+/.
1
3i
c.325-1G>C
r.spl
p.?
-
pathogenic (recessive)
g.104190806C>G
g.101428524C>G
g.8180G>C
-
ALDOB_000055
-
PubMed: Esposito 2004
,
PubMed: Esposito 2010
-
-
Germline
-
1/244 chromosomes (cases)
-
-
-
Johan den Dunnen
+/.
1
4
c.331C>T
r.(?)
p.(Gln111*)
-
pathogenic (recessive)
g.104190799G>A
g.101428517G>A
-
-
ALDOB_000054
-
PubMed: Esposito 2004
,
PubMed: Esposito 2010
-
-
Germline
-
1/244 chromosomes (cases)
-
-
-
Johan den Dunnen
+/.
2
4
c.345_372del
r.(?)
p.(Leu116Phefs*28)
-
pathogenic (recessive)
g.104190760_104190787del
g.101428478_101428505del
345-72del28
-
ALDOB_000053
unknown variant 2nd chromosome
PubMed: Esposito 2010
,
PubMed: Santer 2005
-
-
Germline
-
1/144 chromosomes cases, 1/244 chromosomes (cases)
-
-
-
Johan den Dunnen
?/.
1
-
c.352G>A
r.(?)
p.(Gly118Arg)
-
VUS
g.104190778C>T
-
ALDOB(NM_000035.4):c.352G>A (p.G118R)
-
ALDOB_000072
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Groningen
+/., +?/.
18
4
c.360_363del
r.(?)
p.(Asn120Lysfs*32)
ACMG
likely pathogenic, pathogenic, pathogenic (recessive)
g.104190773_104190776del
g.101428491_101428494del
357delAAAC, 360-363delCAAA, 360-3delCAAA, ALDOB, NM_000035.3, c.360_363del, p.Asn120Lysfs*32, del4E4,
1 more item
-
ALDOB_000002
homozygous, unknown variant 2nd chromosome
PubMed: Alfares 2018
,
PubMed: Coffee 2010
,
PubMed: Davit-Spraul 2008
,
PubMed: Dazzo 1990
,
7 more items
-
rs1800546
Germline, Unknown
?
1/52 chromosomes cases, 1/92 cases, 11/244 chromosomes (cases), 4/144 chromosomes cases,
2 more items
-
-
-
Johan den Dunnen
,
Daniel Trujillano
+?/.
1
-
c.379+1G>T
r.spl?
p.?
-
likely pathogenic
g.104190750C>A
g.101428468C>A
-
-
ALDOB_000013
1 heterozygous, no homozygous;
Clinindb (India)
PubMed: Narang 2020
,
Journal: Narang 2020
-
rs138121153
Germline
-
1/2795 individuals
-
-
-
Mohammed Faruq
?/.
1
5
c.400C>A
r.(?)
p.(Arg134Ser)
-
VUS
g.104189904G>T
g.101427622G>T
-
-
ALDOB_000052
no variant 2nd chromosome
PubMed: Santer 2005
-
-
Germline
-
-
-
-
-
Johan den Dunnen
+/.
1
5
c.403T>C
r.(?)
p.(Cys135Arg)
-
pathogenic (recessive)
g.104189901A>G
g.101427619A>G
C134R
-
ALDOB_000051
-
PubMed: Brooks 1994
-
-
Germline
-
-
-
-
-
Johan den Dunnen
?/.
1
-
c.422A>T
r.(?)
p.(Asp141Val)
-
VUS
g.104189882T>A
g.101427600T>A
ALDOB(NM_000035.4):c.422A>T (p.D141V)
-
ALDOB_000010
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Groningen
+/.
1
5
c.442T>C
r.(?)
p.(Trp148Arg)
-
pathogenic (recessive)
g.104189862A>G
g.101427580A>G
W147R
-
ALDOB_000050
-
PubMed: Ali 1995
-
-
Germline
-
-
-
-
-
Johan den Dunnen
+/.
1
5
c.444G>A
r.(?)
p.(Trp148*)
-
pathogenic (recessive)
g.104189860C>T
g.101427578C>T
-
-
ALDOB_000049
-
PubMed: Davit-Spraul 2008
-
-
Germline
-
1/92 cases
-
-
-
Johan den Dunnen
+/., +?/.
104
5
c.448G>C
r.(?)
p.(Ala150Pro)
-
likely pathogenic, pathogenic, pathogenic (recessive)
g.104189856C>G
g.101427574C>G
A149P, A150P, ALDOB(NM_000035.4):c.448G>C (p.A150P)
-
ALDOB_000006
4 heterozygous, no homozygous;
Clinindb (India)
, no variant 2nd chromosome,
2 more items
PubMed: Ali 1994
,
PubMed: Ali 1994
,
PubMed: Ali 1995
,
PubMed: Ali 1996
,
PubMed: Ali 1998
,
14 more items
-
rs1800546
CLASSIFICATION record, Germline, Unknown
-
17/2000 controls, 29/42 chromosomes cases, 32/52 chromosomes cases, 4/2795 individuals, 73/92 cases,
2 more items
-
-
-
Johan den Dunnen
,
VKGL-NL_Rotterdam
,
VKGL-NL_Groningen
,
VKGL-NL_Utrecht
,
VKGL-NL_Nijmegen
,
VKGL-NL_VUmc
,
Mohammed Faruq
,
MobiDetails
-?/.
1
-
c.468C>T
r.(?)
p.(Asp156=)
-
likely benign
g.104189836G>A
g.101427554G>A
ALDOB(NM_000035.4):c.468C>T (p.D156=)
-
ALDOB_000004
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Groningen
?/.
1
5
c.488C>T
r.(?)
p.(Ala163Val)
-
VUS
g.104189816G>A
g.101427534G>A
-
-
ALDOB_000047
no variant 2nd chromosome
PubMed: Santer 2005
-
-
Germline
-
-
-
-
-
Johan den Dunnen
+/.
1
5
c.497A>T
r.(?)
p.(Glu166Val)
-
pathogenic (recessive)
g.104189807T>A
g.101427525T>A
-
-
ALDOB_000046
unknown variant 2nd chromosome
PubMed: Esposito 2010
-
-
Germline
-
1/244 chromosomes (cases)
-
-
-
Johan den Dunnen
+/.
2
5
c.522C>G
r.(?)
p.(Tyr174*)
-
pathogenic (recessive)
g.104189782G>C
g.101427500G>C
-
-
ALDOB_000045
-
PubMed: Gruchota 2006
-
-
Germline
-
2/52 chromosomes cases
-
-
-
Johan den Dunnen
+/., +?/.
41
5
c.524C>A
r.(?)
p.(Ala175Asp)
-
likely pathogenic, pathogenic, pathogenic (recessive)
g.104189780G>T
g.101427498G>T
A174D, A175D, ALDOB(NM_000035.4):c.524C>A (p.A175D), NM_000035.3:c.524C>A; p.Ala175Asp
-
ALDOB_000009
no variant 2nd chromosome, unknown variant 2nd chromosome, VKGL data sharing initiative Nederland
PubMed: Ali 1994
,
PubMed: Ali 1995
,
PubMed: Cross 1990
,
PubMed: Cross 1990
,
PubMed: Davit-Spraul 2008
,
8 more items
-
rs76917243
CLASSIFICATION record, Germline, Unknown
?
16/144 chromosomes cases, 21/92 cases, 3/2000 controls, 3/52 chromosomes cases, 4/42 chromosomes cases,
1 more item
-
-
-
Johan den Dunnen
,
VKGL-NL_Groningen
,
VKGL-NL_Nijmegen
,
MobiDetails
+/.
1
5
c.532T>C
r.(?)
p.(Cys178Arg)
-
pathogenic (recessive)
g.104189772A>G
g.101427490A>G
-
-
ALDOB_000044
unknown variant 2nd chromosome
PubMed: Santer 2005
-
-
Germline
-
1/144 chromosomes cases
-
-
-
Johan den Dunnen
?/.
1
5
c.538C>A
r.(?)
p.(Gln180Lys)
-
VUS
g.104189766G>T
g.101427484G>T
-
-
ALDOB_000043
no variant 2nd chromosome
PubMed: Santer 2005
-
-
Germline
-
-
-
-
-
Johan den Dunnen
+/.
1
5i
c.540+1G>C
r.spl
p.?
-
pathogenic (recessive)
g.104189763C>G
g.101427481C>G
IVS5+1G>C
-
ALDOB_000042
-
PubMed: Ali 1996
-
-
Germline
-
-
-
-
-
Johan den Dunnen
+/.
1
5i_7i
c.541-154_800-178del
r.spl
p.?
-
pathogenic (recessive)
g.104187503_104189075del
g.101425221_101426793del
g.8989-10457del
-
ALDOB_000027
1469 bp deletion from IVS5 to IVS7
PubMed: Cross 1990
-
-
Germline
-
-
-
-
-
Johan den Dunnen
+/.
1
6
c.548_552del
r.(?)
p.(Leu183Profs*4)
-
pathogenic (recessive)
g.104188909_104188913del
g.101426627_101426631del
-
-
ALDOB_000040
unknown variant 2nd chromosome
PubMed: Esposito 2010
-
-
Germline
-
1/244 chromosomes (cases)
-
-
-
Johan den Dunnen
+/.
1
6
c.548_553del
r.(?)
p.(Leu183_Val184del)
-
pathogenic (recessive)
g.104188910_104188915del
g.101426628_101426633del
g10072–10077delTGGTAC
-
ALDOB_000041
-
PubMed: Santamaria 1999
-
-
Germline
-
-
-
-
-
Johan den Dunnen
+/.
1
6
c.554C>G
r.(?)
p.(Pro185Arg)
-
pathogenic (recessive)
g.104188907G>C
g.101426625G>C
g.4271C>G
-
ALDOB_000039
-
PubMed: Sanchez-Gutierrez 2002
-
-
Germline
-
1/42 chromosomes cases
-
-
-
Johan den Dunnen
+/.
6
6
c.612T>A
r.(?)
p.(Tyr204*)
-
pathogenic (recessive)
g.104188849A>T
g.101426567A>T
Y203X, Y204X
-
ALDOB_000037
unknown variant 2nd chromosome
PubMed: Ali 1993
,
PubMed: Esposito 2010
,
PubMed: Gruchota 2006
,
PubMed: Santamaria 1996
,
1 more item
-
-
Germline
-
1/144 chromosomes cases, 1/52 chromosomes cases, 19/244 chromosomes (cases)
-
-
-
Johan den Dunnen
+/.
1
6
c.612T>G
r.(?)
p.(Tyr204*)
-
pathogenic (recessive)
g.104188849A>C
g.101426567A>C
-
-
ALDOB_000038
unknown variant 2nd chromosome
PubMed: Santer 2005
-
-
Germline
-
1/144 chromosomes cases
-
-
-
Johan den Dunnen
?/.
1
-
c.619G>C
r.(?)
p.(Glu207Gln)
-
VUS
g.104188842C>G
g.101426560C>G
-
-
ALDOB_000012
conflicting interpretations of pathogenicity; 12 heterozygous, no homozygous;
Clinindb (India)
PubMed: Narang 2020
,
Journal: Narang 2020
-
rs3739721
Germline
-
12/2791 individuals
-
-
-
Mohammed Faruq
+/.
2
6i
c.625-2A>G
r.spl
p.?
-
pathogenic (recessive)
g.104187911T>C
g.101425629T>C
-
-
ALDOB_000035
-
PubMed: Esposito 2004
,
PubMed: Esposito 2010
-
-
Germline
-
2/244 chromosomes (cases)
-
-
-
Johan den Dunnen
+/.
2
6i
c.625-1G>A
r.spl
p.?
-
pathogenic (recessive)
g.104187910C>T
g.101425628C>T
IVS6-1G>A
-
ALDOB_000034
unknown variant 2nd chromosome
PubMed: Ali 1994
,
PubMed: Davit-Spraul 2008
-
-
Germline
-
1/92 cases
-
-
-
Johan den Dunnen
+/.
1
7
c.664G>T
r.(?)
p.(Val222Phe)
-
pathogenic (recessive)
g.104187870C>A
g.101425588C>A
-
-
ALDOB_000033
-
PubMed: Esposito 2004
,
PubMed: Esposito 2010
-
-
Germline
-
1/244 chromosomes (cases)
-
-
-
Johan den Dunnen
+/.
1
7
c.686T>C
r.(?)
p.(Leu229Pro)
-
pathogenic (recessive)
g.104187848A>G
g.101425566A>G
-
-
ALDOB_000032
-
PubMed: Esposito 2004
,
PubMed: Esposito 2010
-
-
Germline
-
1/244 chromosomes (cases)
-
-
-
Johan den Dunnen
+/.
1
7
c.689_690insTGCTAA
r.(?)
p.(Leu229_Lys230insAsnAla)
-
pathogenic (recessive)
g.104187844_104187845insTTAGCA
g.101425562_101425563insTTAGCA
K230MfsX136
-
ALDOB_000031
-
PubMed: Davit-Spraul 2008
-
-
Germline
-
1/92 cases
-
-
-
Johan den Dunnen
+/.
1
-
c.709G>T
r.(?)
p.(Gly237*)
-
pathogenic
g.104187825C>A
-
ALDOB(NM_000035.4):c.709G>T (p.G237*)
-
ALDOB_000074
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Utrecht
+/.
1
7
c.720C>A
r.(?)
p.(Cys240*)
-
pathogenic (recessive)
g.104187814G>T
g.101425532G>T
-
-
ALDOB_000030
-
PubMed: Kajihara 1990
-
-
Germline
-
-
-
-
-
Johan den Dunnen
?/.
1
-
c.736C>T
r.(?)
p.(Pro246Ser)
-
VUS
g.104187798G>A
g.101425516G>A
ALDOB(NM_000035.4):c.736C>T (p.P246S)
-
ALDOB_000003
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Rotterdam
+/.
3
7
c.770T>C
r.(?)
p.(Leu257Pro)
-
pathogenic (recessive)
g.104187764A>G
g.101425482A>G
L256P
-
ALDOB_000029
unknown variant 2nd chromosome
PubMed: Ali 1994
,
PubMed: Esposito 2010
,
PubMed: Santamaria 1996
-
-
Germline
-
5/244 chromosomes (cases)
-
-
-
Johan den Dunnen
+/.
1
7i
c.799+2T>A
r.spl
p.?
-
pathogenic (recessive)
g.104187733A>T
g.101425451A>T
IVS7+2T>A
-
ALDOB_000028
unknown variant 2nd chromosome
PubMed: Santer 2005
-
-
Germline
-
2/144 chromosomes cases
-
-
-
Johan den Dunnen
+/.
1
8
c.839C>A
r.(?)
p.(Ala280Asp)
-
pathogenic (recessive)
g.104187285G>T
g.101425003G>T
-
-
ALDOB_000026
-
PubMed: Davit-Spraul 2008
-
-
Germline
-
1/92 cases
-
-
-
Johan den Dunnen
+/.
1
8
c.841_842del
r.(?)
p.(Thr281Serfs*54)
-
pathogenic (recessive)
g.104187283_104187284del
g.101425001_101425002del
841-2delAC
-
ALDOB_000025
unknown variant 2nd chromosome
PubMed: Santer 2005
-
-
Germline
-
2/144 chromosomes cases
-
-
-
Johan den Dunnen
+/.
1
8
c.851T>C
r.(?)
p.(Leu284Pro)
-
pathogenic (recessive)
g.104187273A>G
g.101424991A>G
-
-
ALDOB_000024
unknown variant 2nd chromosome
PubMed: Santer 2005
-
-
Germline
-
1/144 chromosomes cases
-
-
-
Johan den Dunnen
+/.
4
8
c.865del
r.(?)
p.(Leu289Phefs*10)
-
pathogenic (recessive)
g.104187260del
g.101424978del
865delC, L288delC
-
ALDOB_000023
unknown variant 2nd chromosome
PubMed: Cross 1990
,
PubMed: Esposito 2010
,
PubMed: Santer 2005
-
-
Germline
-
1/244 chromosomes (cases), 2/144 chromosomes cases
-
-
-
Johan den Dunnen
+/., ?/.
2
-
c.887G>A
r.(?)
p.(Trp296Ter)
-
pathogenic, VUS
g.104187237C>T
g.101424955C>T
ALDOB(NM_000035.3):c.887G>A (p.(Trp296Ter))
-
ALDOB_000005
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Leiden
,
VKGL-NL_Nijmegen
+/.
3
8
c.910C>T
r.(?)
p.(Arg304Trp)
-
pathogenic (recessive)
g.104187214G>A
g.101424932G>A
R303W
-
ALDOB_000022
unknown variant 2nd chromosome
PubMed: Esposito 2010
,
PubMed: Santamaria 1996
,
PubMed: Tolan 1995
, Cox ASHG1991
-
-
Germline
-
1/244 chromosomes (cases)
-
-
-
Johan den Dunnen
+/., ?/.
3
8
c.911G>A
r.(?)
p.(Arg304Gln)
-
pathogenic (recessive), VUS
g.104187213C>T
g.101424931C>T
g.11125G>A
-
ALDOB_000001
unknown variant 2nd chromosome
PubMed: Esposito 2010
,
PubMed: Santamaria 2000
-
-
Germline
-
1/244 chromosomes (cases)
-
-
-
Gerard C.P. Schaafsma
,
Johan den Dunnen
+/.
1
8
c.932T>C
r.(?)
p.(Leu311Pro)
-
pathogenic (recessive)
g.104187192A>G
g.101424910A>G
-
-
ALDOB_000021
-
PubMed: Davit-Spraul 2008
-
-
Germline
-
1/92 cases
-
-
-
Johan den Dunnen
+/.
3
8
c.954_995del
r.(?)
p.(Ala319_Ala332del)
-
pathogenic (recessive)
g.104187132_104187173del
g.101424850_101424891del
953_994del42
-
ALDOB_000020
-
PubMed: Davit-Spraul 2008
-
-
Germline
-
3/92 cases
-
-
-
Johan den Dunnen
+/.
1
8i_9
c.1000-1_1006delinsTG
r.spl
p.?
-
pathogenic (recessive)
g.104184180_104184187delinsCA
g.101421898_101421905delinsCA
-
-
ALDOB_000018
-
PubMed: Ali 1994
-
-
Germline
-
-
-
-
-
Johan den Dunnen
+/.
20
9
c.1005C>G
r.(?)
p.(Asn335Lys)
-
pathogenic, pathogenic (recessive)
g.104184181G>C
g.101421899G>C
N334K, N335K
-
ALDOB_000019
no variant 2nd chromosome, unknown variant 2nd chromosome, VKGL data sharing initiative Nederland
PubMed: Ali 1994
,
PubMed: Coffee 2010
,
PubMed: Cross 1990
,
PubMed: Davit-Spraul 2008
,
8 more items
-
rs78340951
CLASSIFICATION record, Germline
-
1/2000 controls, 1/42 chromosomes cases, 1/73,755 controls, 11/144 chromosomes cases, 7/92 cases,
1 more item
-
-
-
Johan den Dunnen
,
VKGL-NL_Nijmegen
+/.
6
9
c.1013C>T
r.(?)
p.(Ala338Val)
-
pathogenic (recessive)
g.104184173G>A
g.101421891G>A
A337V
-
ALDOB_000017
unknown variant 2nd chromosome
PubMed: Ali 1998
,
PubMed: Davit-Spraul 2008
,
PubMed: Esposito 2010
,
PubMed: Relos 1999
-
-
Germline
-
2/244 chromosomes (cases), 4/92 cases
-
-
-
Johan den Dunnen
+/.
1
9
c.1027T>C
r.(?)
p.(Tyr343His)
-
pathogenic (recessive)
g.104184159A>G
g.101421877A>G
-
-
ALDOB_000016
unknown variant 2nd chromosome
PubMed: Esposito 2010
-
-
Germline
-
1/244 chromosomes (cases)
-
-
-
Johan den Dunnen
+/.
1
9
c.1044_1049delinsACACT
r.(?)
p.(Ser349Hisfs*24)
-
pathogenic (recessive)
g.104184137_104184142delinsAGTGT
g.101421855_101421860delinsAGTGT
1044_1049delTTCTGGinsACACT
-
ALDOB_000015
unknown variant 2nd chromosome
PubMed: Santer 2005
-
-
Germline
-
1/144 chromosomes cases
-
-
-
Johan den Dunnen
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