Global Variome shared LOVD
AIPL1 (aryl hydrocarbon receptor interacting protei...)
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Global Variome, with Curator vacancy
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Unique variants in the AIPL1 gene
This database is one of the
"Eye disease"
gene variant databases.
The variants shown are described using the NM_014336.3 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
all entries containing 'Arg' and 'Ser'
|
Text
Arg|Ser
all entries containing 'Arg' or 'Ser'
!
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'
To sort on a certain column, click on the column header or on the arrows. If that column is already selected to sort on, the sort order will be swapped. The column currently sorted on has a darker blue background color than the other columns. The up and down arrows next to the column name indicate the current sorting direction. When sorting on any field other than the default, LOVD will sort secondarily on the default sort column.
163 entries on 2 pages. Showing entries 1 - 100.
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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
1i
c.-106C>A
r.(?)
p.(=)
-
likely benign
g.6338530G>T
g.6435210G>T
1-106C>A IVS1-106C>A
-
AIPL1_000005
homozygous SNP
PubMed: Tan 2012
-
rs7211442
Unknown
-
-
-
-
-
Raheel Qamar
-/.
1
-
c.-17C>A
r.(?)
p.(=)
-
benign
g.6338441G>T
g.6435121G>T
AIPL1(NM_014336.5):c.-17C>A
-
AIPL1_000182
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_AMC
+?/.
1
-
c.(?_-1)_(276+1_277-1)del
r.(?)
p.(?)
ACMG
likely pathogenic
g.?
g.?
AIPL1 c.(?_-1) _(276+1_277-1)del, c.815G>C, p.(Arg272Pro)
-
MYH2_000008
-
PubMed: Jespersgaar 2019
-
-
Germline
?
-
-
-
-
LOVD
+?/., -?/.
11
6
c.?
r.(?), r.?
p.?, p.Leu241del, p.Val33fs
-
likely benign, likely pathogenic, likely pathogenic (recessive)
g.6319593C>T, g.?
-
AF148864:111T>C (TTT?TTC) Phe37Phe, AF148864:287C>T (TGC?TGT) Cys89Cys, c.10342G>A,
7 more items
-
AIPL1_000000, MYH2_000008
-
PubMed: Eisenberger-2013
,
PubMed: Jacobson 2011
,
PubMed: Sohocki 2001
,
PubMed: Wang 2016
-
-
CLASSIFICATION record, Germline
-
-
-
-
-
Julia Lopez
+?/.
1
-
c.34dup
r.(?)
p.(Val12Glyfs*32)
-
likely pathogenic
g.6338394dup
g.6435074dup
AIPL1, variant 1: c.34dup/p.V12Gfs*32, variant 2: c.238C>T/p.R80W
-
AIPL1_000209
possibly solved, compound heterozygous
PubMed: Weisschuh 2020
-
-
Unknown
?
-
-
-
-
LOVD
+/., +?/.
6
1
c.50T>C
r.(?)
p.(Leu17Pro)
-
likely pathogenic, pathogenic
g.6338375A>G
g.6435055A>G
AIPL1, variant 1: c.50T>C/p.L17P, variant 2: c.50T>C/p.L17P, c.50T>C, Leu17Pro, p.Leu17Pro
-
AIPL1_000019
compound heterozygous missense variant, solved, homozygous
PubMed: Eisenberger-2013
,
PubMed: Pennesi 2011
,
PubMed: Weisschuh 2020
-
-
Germline, Unknown
?
-
-
-
-
Raheel Qamar
-?/.
2
1
c.51G>A
r.(?)
p.(=)
-
likely benign
g.6338374C>T
g.6435054C>T
-
-
AIPL1_000023
homozygous missense variant
PubMed: Tan 2012
-
-
Unknown
-
-
-
-
-
Raheel Qamar
-?/.
1
-
c.86C>A
r.(?)
p.(Thr29Asn)
-
likely benign
g.6338339G>T
-
AIPL1(NM_014336.4):c.86C>A (p.T29N)
-
AIPL1_000204
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Rotterdam
-?/.
2
2i
c.97-16C>T
r.(?)
p.(=)
-
likely benign
g.6337434G>A
g.6434114G>A
-
-
AIPL1_000031
homozygous splice site variant
PubMed: Tan 2012
-
-
Unknown
-
-
-
-
-
Raheel Qamar
-?/.
1
-
c.97-15C>T
r.(=)
p.(=)
-
likely benign
g.6337433G>A
g.6434113G>A
AIPL1(NM_014336.5):c.97-15C>T
-
AIPL1_000172
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_AMC
-/., -?/.
4
1i
c.97-9G>A
r.(=), r.(?)
p.(=)
-
benign, likely benign
g.6337427C>T
g.6434107C>T
AIPL1(NM_014336.4):c.97-9G>A, AIPL1(NM_014336.5):c.97-9G>A, IVS1-9 G>A
-
AIPL1_000029
SNP, VKGL data sharing initiative Nederland
PubMed: Sohocki 2000
-
-
CLASSIFICATION record, Germline
-
-
-
-
-
Raheel Qamar
,
VKGL-NL_Rotterdam
,
VKGL-NL_AMC
+/.
5
2
c.97_104dup
r.(?), r.(spl?)
p.(Phe35Leufs*2)
ACMG
pathogenic
g.6337411_6337418dup
g.6434091_6434098dup
96_97insGTGATCTT, AIPL1:NM_014336 c.97_104dup, p.(Phe35Leufs*2), c.97_104dup; p.(Phe35Leufs*2)
-
AIPL1_000025
compound heterozygous deleterious variant, homozygous, individual solved, variant causal,
1 more item
PubMed: Rodriguez-Munoz 2020
,
PubMed: Testa 2011
-
-
Germline
yes
-
NotI-HindIII
-
-
Raheel Qamar
?/.
1
-
c.98T>C
r.(?)
p.(Val33Ala)
-
VUS
g.6337417A>G
-
AIPL1(NM_014336.5):c.98T>C (p.(Val33Ala))
-
AIPL1_000232
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Leiden
+/.
1
-
c.99del
r.(?)
p.(Ile34Serfs*7)
ACMG
pathogenic
g.6337416del
-
-
-
AIPL1_000187
-
PubMed: Sharon 2019
-
-
Germline
-
1/2420 IRD families
-
-
-
Global Variome, with Curator vacancy
-/., -?/.
5
2
c.111C>T
r.(?)
p.(=), p.(Phe37=)
-
benign, likely benign
g.6337404G>A
g.6434084G>A
TTT>TTC
-
AIPL1_000033
homozygous SNP, polymorphisms silent substitution, VKGL data sharing initiative Nederland
PubMed: Sohocki 2000
,
PubMed: Tan 2012
-
rs11650007
CLASSIFICATION record, Germline, Unknown
-
-
-
-
-
Raheel Qamar
,
VKGL-NL_Nijmegen
+?/.
5
2
c.112del
r.(?)
p.(Arg38Alafs*3)
-
likely pathogenic
g.6337404del
g.6434084del
111delC,
1 more item
-
AIPL1_000035
compound heterozygous, homozygous frameshift variant
PubMed: Martin Merida 2019
,
PubMed: Vallespin 2007Â
-
-
Germline
yes
-
-
-
-
Raheel Qamar
+/., +?/.
15
2
c.116C>A
r.(?)
p.(Thr39Asn)
-
likely pathogenic (recessive), pathogenic
g.6337399G>T
g.6434079G>T
116C>A / Thr39Asp, c.116C>A, c.116C>A; p.T39N, C>A 116
-
AIPL1_000041
homozygous missense variant
Khaliq 2003, Roosing 2017,
PubMed: Khaliq 2002
,
PubMed: Khaliq 2003
-
-
Germline
yes
-
-
-
-
Julia Lopez
,
Raheel Qamar
+/.
1
2
c.126T>A
r.(?)
p.(Cys42*)
-
pathogenic
g.6337389A>T
g.6434069A>T
Cys42X
-
AIPL1_000051
heterozygous deleterious variant
PubMed: Dharmaraj 2004
-
-
Germline
-
-
-
-
-
Raheel Qamar
-?/.
1
-
c.134A>G
r.(?)
p.(Glu45Gly)
-
likely benign
g.6337381T>C
g.6434061T>C
AIPL1(NM_014336.5):c.134A>G (p.E45G)
-
AIPL1_000171
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_AMC
-/., -?/., ?/.
3
-
c.140C>G
r.(?)
p.(Thr47Arg)
-
benign, likely benign, VUS
g.6337375G>C
g.6434055G>C
AIPL1(NM_014336.4):c.140C>G (p.T47R), AIPL1(NM_014336.5):c.140C>G (p.T47R)
-
AIPL1_000170
VKGL data sharing initiative Nederland
PubMed: Wang 2014
-
-
CLASSIFICATION record, Germline
-
-
-
-
-
VKGL-NL_Rotterdam
,
VKGL-NL_AMC
-?/.
1
-
c.146T>C
r.(?)
p.(Ile49Thr)
-
likely benign
g.6337369A>G
g.6434049A>G
AIPL1(NM_014336.5):c.146T>C (p.I49T)
-
AIPL1_000169
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_AMC
+/., +?/., ?/.
5
2
c.152A>G
r.(?)
p.(Asp51Gly), p.(Glu51Gly)
ACMG
likely pathogenic, likely pathogenic (recessive), pathogenic, VUS
g.6337363T>C
g.6434043T>C
AIPL1 NM_014336: g.1157A>G, c.152A>G, p.D51G, c.152A>G, c.152A>G, p.Asp51Gly
-
AIPL1_000196
heterozygous
PubMed: Gao 2019
,
PubMed: Liu-2020
,
PubMed: Wang 2015
,
PubMed: Xu 2020
-
-
Germline
?, yes
-
-
-
-
LOVD
+/.
1
2
c.157C>T
r.(?)
p.(Arg53Trp)
-
pathogenic
g.6337358G>A
-
c.157C>T; p.R53W
-
AIPL1_000218
-
Li 2013
-
-
Germline
-
-
-
-
-
LOVD
+?/.
3
-
c.178dup
r.(?)
p.(His60Profs*98), p.(His60ProfsTer98)
ACMG
likely pathogenic
g.6337337dup
g.6434017dup
-
-
AIPL1_000157
-
PubMed: Patel 2016
,
PubMed: Trujillano 2017
-
-
Germline
-
-
-
-
-
Daniel Trujillano
+/.
2
2
c.190G>A
r.(?)
p.(Gly64Arg)
-
pathogenic
g.6337325C>T
g.6434005C>T
p.Gly64Arg
-
AIPL1_000053
compound heterozygous missense variant
PubMed: Tan 2012
-
-
Germline
-
0.003 in 153 patients; 0 in 96 controls
-
-
-
Raheel Qamar
+/., +?/., ?/.
18
2, 3
c.211G>T
r.(?)
p.(Val71Phe)
ACMG
likely pathogenic, pathogenic (recessive), VUS
g.6337304C>A
g.6433984C>A
c.211G>T, p.Val71Phe, Val71Phe
-
AIPL1_000055
compound heterozygous missense variant, homozygous missense variant
PubMed: Beryozkin 2015
,
PubMed: Sharon 2019
,
PubMed: Hanein 2004
,
PubMed: Jacobson 2011
,
2 more items
-
-
Germline, Unknown
-
8/2420 IRD families
-
-
-
Global Variome, with Curator vacancy
,
Raheel Qamar
,
Dror Sharon
,
Daan Panneman
+/., +?/.
4
2, 3
c.214T>C
r.(?), r.?
p.(Trp72Arg), p.Trp72Arg
-
likely pathogenic, pathogenic
g.6337301A>G
g.6433981A>G
c.214T>C, c.214T>C; p.W72R, p.Trp72Arg, Trp72Arg
-
AIPL1_000061
compound heterozygous missense variant
Wiszniewski 2011,
PubMed: Jacobson 2011
,
PubMed: Wang-2013
-
-
Germline, Unknown
-
-
-
-
-
Raheel Qamar
+/.
1
-
c.215G>A
r.(?)
p.(Trp72*)
ACMG
pathogenic
g.6337300C>T
-
-
-
AIPL1_000186
-
PubMed: Sharon 2019
-
-
Germline
-
1/2420 IRD families
-
-
-
Global Variome, with Curator vacancy
+?/.
2
2, 3
c.216G>A
r.(?)
p.(Trp72*)
-
likely pathogenic
g.6337299C>T
g.6433979C>T
p.Trp72X
-
AIPL1_000058
compound heterozygous missense variant
PubMed: Jacobson 2011
-
-
Germline
-
-
-
-
-
Raheel Qamar
-/., -?/.
4
2, 3
c.234C>T
r.(?)
p.(=), p.(Ser78=)
-
benign, likely benign
g.6337281G>A
g.6433961G>A
AF148864:234C>T (TCC?TCT) Ser78Ser, AIPL1(NM_014336.4):c.234C>T (p.S78=), TCC>TCT
-
AIPL1_000065
polymorphisms silent substitution, VKGL data sharing initiative Nederland
PubMed: Sohocki 2000
,
PubMed: Sohocki 2001
-
-
CLASSIFICATION record, Germline
-
-
-
-
-
Julia Lopez
,
Raheel Qamar
,
VKGL-NL_Rotterdam
+/., ?/.
10
2
c.236T>C
r.(?)
p.(Met79Thr)
-
pathogenic, VUS
g.6337279A>G
g.6433959A>G
236T>C (ATG > ACG), M79T, Met79Thr
-
AIPL1_000067
compound heterozygous, homozygous deleterious variant, homozygous substitution
PubMed: Dharmaraj 2004
,
PubMed: Galvin 2005
,
PubMed: Sohocki 2000
-
-
Germline
-
-
-
-
-
Raheel Qamar
+?/.
1
-
c.238C>T
r.(?)
p.(Arg80Trp)
-
likely pathogenic
g.6337277G>A
g.6433957G>A
AIPL1, variant 1: c.34dup/p.V12Gfs*32, variant 2: c.238C>T/p.R80W
-
AIPL1_000208
possibly solved, compound heterozygous
PubMed: Weisschuh 2020
-
-
Unknown
?
-
-
-
-
LOVD
+?/., -?/., ?/.
7
2, 3
c.244C>T
r.(?)
p.(His82Tyr)
-
likely benign, likely pathogenic, VUS
g.6337271G>A
g.6433951G>A
244C>T, AIPL1(NM_014336.5):c.244C>T (p.H82Y), H82Y (244C>T)
-
AIPL1_000077
homozygous missense variant, VKGL data sharing initiative Nederland
PubMed: Heegaard 2003
,
PubMed: HeegaarD2003
,
PubMed: Tiwari 2016
-
-
CLASSIFICATION record, Germline
-
-
-
-
-
Raheel Qamar
,
VKGL-NL_AMC
+/.
3
2
c.247G>A
r.(?)
p.(Glu83Lys)
-
pathogenic, pathogenic (recessive)
g.6337268C>T
g.6433948C>T
-
-
AIPL1_000014
-
PubMed: Srilekha 2015
-
-
Germline
yes
2/200
-
-
-
Soumittra Nagasamy
+/., ?/.
10
2, 3
c.264G>A
r.(?)
p.(Trp88*)
-
pathogenic, VUS
g.6337251C>T
g.6433931C>T
264G> A (TGG>TGA), p.Trp88Ter, Trp88X
-
AIPL1_000081
homozygous, homozygous deleterious variant, homozygous missense variant
PubMed: Dharmaraj 2004
,
PubMed: Sohocki 2000
,
PubMed: Tan 2012
-
-
Germline
-
0.013 in 153 patients; 0 in 96 controls
-
-
-
Raheel Qamar
+/., +?/.
5
2, 3
c.265T>C
r.(?), r.?
p.(Cys89Arg)
-
likely pathogenic, pathogenic
g.6337250A>G
g.6433930A>G
c.265T>C, Cys89Arg, p.Cys89Arg
-
AIPL1_000062
compound heterozygous missense variant, VKGL data sharing initiative Nederland
PubMed: Ellingford 2016
,
PubMed: Jacobson 2011
,
PubMed: Wang-2013
-
-
CLASSIFICATION record, Germline, Unknown
-
-
-
-
-
Raheel Qamar
,
VKGL-NL_Nijmegen
+/., +?/., ?/.
4
3
c.266G>A
r.(?)
p.(Cys89Tyr)
-
likely pathogenic, pathogenic, VUS
g.6337249C>T
g.6433929C>T
AIPL1 c.266G>A, p.C89Y, AIPL1(NM_001033054.1):c.266G>A (p.(Cys89Tyr)), c.266G>A,
1 more item
-
AIPL1_000181
homozygous, VKGL data sharing initiative Nederland
Kaway 2017, Wiszniewski 2011,
PubMed: Wiszniewski 2011
-
-
CLASSIFICATION record, Germline, Unknown
?
-
-
-
-
VKGL-NL_Leiden
-/., -?/.
6
2
c.267C>T
r.(?)
p.(=), p.(Cys89=)
-
benign, likely benign
g.6337248G>A
g.6433928G>A
287C>T TGC>TGT (C89C),
1 more item
-
AIPL1_000082
homozygous missense variant, polymorphisms silent substitution, VKGL data sharing initiative Nederland
PubMed: Sohocki 2000
,
PubMed: Tan 2012
-
-
CLASSIFICATION record, Germline, Unknown
-
-
-
-
-
Raheel Qamar
,
VKGL-NL_Rotterdam
,
VKGL-NL_AMC
+/., +?/., -/., -?/.
13
2, 3
c.268G>C
r.(?)
p.(Asp90His)
-
benign, likely benign, likely pathogenic
g.6337247C>G
g.6433927C>G
286G>C, Asp90His, c.268G>C
-
AIPL1_000078
homozygous neutral SNP, polymorphisms silent substitution, SNP, VKGL data sharing initiative Nederland
PubMed: HeegaarD2003
,
PubMed: Jonsson-2013
,
PubMed: Sohocki 2000
,
PubMed: Sohocki 2001
,
1 more item
-
rs12449580
CLASSIFICATION record, Germline, Unknown
-
-
-
-
-
Julia Lopez
,
Raheel Qamar
,
VKGL-NL_Nijmegen
?/.
1
-
c.276+6T>C
r.spl?
p.(?)
ACMG
VUS
g.6337233A>G
g.6433913A>G
allele 1: c.834G>A/p.W278*, allele 2: c.276+6T>C/p.?
-
AIPL1_000203
heterozygous
PubMed: Weisschuh 2018
-
-
Germline
?
-
-
-
-
LOVD
-/.
2
2i
c.276+66G>C
r.(?)
p.(=)
-
benign
g.6337173C>G
g.6433853C>G
IVS2+66 G>C
-
AIPL1_000079
SNP
PubMed: Sohocki 2000
-
-
Germline
-
-
-
-
-
Raheel Qamar
-/.
2
2i
c.277-88C>T
r.(?)
p.(=)
-
benign
g.6331914G>A
g.6428594G>A
IVS2+88 C>T (277+88C>T)
-
AIPL1_000080
SNP
PubMed: Sohocki 2000
-
-
Germline
-
-
-
-
-
Raheel Qamar
-/.
1
-
c.277-10A>C
r.(=)
p.(=)
-
benign
g.6331836T>G
g.6428516T>G
-
-
AIPL1_000175
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Nijmegen
-?/.
3
2i
c.277-10A>G
r.(?)
p.(=)
-
likely benign
g.6331836T>C
g.6428516T>C
IVS2-10G/A
-
AIPL1_000017
homozygous SNP, SNP
PubMed: Sohocki 2000
,
PubMed: Tan 2012
-
rs12453262
Germline, Unknown
-
-
-
-
-
Raheel Qamar
+/., +?/., ?/.
18
2i
c.277-2A>G
r.spl
p.?
ACMG
likely pathogenic, likely pathogenic (recessive), pathogenic, VUS
g.6331828T>C
g.6428508T>C
AIPL1 c.277-2A>G, p.?, c.277-2A>G, IVS2 -2A>G, IVS2-2A>G, IVS2–2A>G, p.IVS2–2A>G
-
AIPL1_000007
compound heterozygous, compound heterozygous splice site variant, heterozygous,
3 more items
PubMed: Dharmaraj 2004
,
PubMed: Galvin 2005
,
PubMed: Hanein 2004
,
PubMed: Jacobson 2011
,
5 more items
-
-
Germline, Germline/De novo (untested)
?
0.003 in 153 patients; 0 in 96 controls
-
-
-
Raheel Qamar
?/.
1
3
c.284G>A
r.(?)
p.(Gly95Glu)
ACMG
VUS
g.6331819C>T
g.6428499C>T
c.284G>A
-
AIPL1_000199
single heterozygous variant in a recessive gene, probably not causative in the patient
PubMed: Hosono 2018
-
rs563684228
Germline
no
-
-
-
-
LOVD
+/., +?/., -/., -?/., ?/.
14
3
c.286G>A
r.(?)
p.(Val96Ile), p.(Val96Met)
-
benign, likely benign, likely pathogenic, pathogenic, VUS
g.6331817C>T
g.6428497C>T
286G>A, 286G>A (GTC>ATC), AIPL1(NM_001033055.1):c.106G>A (p.(Val36Ile)), Val96Ile,
2 more items
-
AIPL1_000001
heterozygous substitution, homozygous deleterious variant, homozygous neutral SNP, predicted benign,
2 more items
PubMed: Booij 2005
,
PubMed: Dharmaraj 2004
,
PubMed: Neveling 2012
,
PubMed: Sohocki 2000
,
3 more items
-
rs62619924
CLASSIFICATION record, Germline, Unknown
-
-
-
-
-
Julia Lopez
,
Kornelia Neveling
,
Raheel Qamar
,
VKGL-NL_Leiden
-/.
1
3
c.286G>C
r.(?)
p.(Val96Leu)
-
benign
g.6331817C>G
-
H90D (286G>C)
-
AIPL1_000217
-
PubMed: Heegaard 2003
-
-
Germline
-
-
-
-
-
LOVD
+?/., -/., -?/.
7
3
c.300A>G
r.(?)
p.(=), p.(Leu100=)
-
benign, likely benign, likely pathogenic
g.6331803T>C
g.6428483T>C
300G>A (CTG/CTA), CTG>CTA (L100L)
-
AIPL1_000068
homozygous SNP, polymorphisms silent substitution, SNP, VKGL data sharing initiative Nederland
PubMed: Sohocki 2000
,
PubMed: Sohocki 2000
,
PubMed: Tan 2012
-
rs8075035
CLASSIFICATION record, Germline, Unknown
-
-
-
-
-
Raheel Qamar
,
VKGL-NL_Nijmegen
?/.
1
-
c.305G>A
r.(?)
p.(Arg102Gln)
-
VUS
g.6331798C>T
g.6428478C>T
AIPL1(NM_014336.4):c.305G>A (p.R102Q)
-
AIPL1_000168
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Rotterdam
?/.
1
-
c.325C>T
r.(?)
p.(Gln109Ter)
-
VUS
g.6331778G>A
g.6428458G>A
-
-
AIPL1_000195
-
PubMed: Wang 2015
-
-
Germline
-
-
-
-
-
LOVD
+/., +?/., -?/., ?/.
19
2, 3
c.341C>T
r.(?)
p.(Thr114Ile)
-
likely benign, likely pathogenic, pathogenic, VUS
g.6331762G>A
g.6428442G>A
341C> T (ACA>ATA), c.341C>T, c.341C>T; p.T114I, T114I, Thr114Ile
-
AIPL1_000075
Authors suggest c.1126C>T (p.P376S) and c.341C>T (p.T114I) are a common haplotype, heterozygous,
4 more items
Dharmaraj 2004, Linnert 2013, Sohocki 2000, Testa 2011, Walia 2010,
PubMed: Dharmaraj 2004
,
5 more items
-
rs8069375
Germline, Unknown
-
1/899 cases
-
-
-
Global Variome, with Curator vacancy
,
Raheel Qamar
-?/.
1
-
c.351C>T
r.(?)
p.(His117=)
-
likely benign
g.6331752G>A
-
AIPL1(NM_014336.4):c.351C>T (p.H117=)
-
AIPL1_000221
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Rotterdam
+?/.
1
-
c.356_359del
r.(?)
p.(His119Argfs*31)
-
likely pathogenic (recessive)
g.6331745_6331748del
g.6428425_6428428del
-
-
AIPL1_000190
-
PubMed: Thompson 2017
-
-
Germline
-
-
-
-
-
LOVD
+/.
1
3
c.364delinsAA
r.(?)
p.(Gly122Lysfs*36)
-
pathogenic
g.6331739delinsTT
g.6428419delinsTT
364G>AA (Gly122fs)
-
AIPL1_000070
AminoAcidchange due to change of different nucleotide
PubMed: Testa 2011
-
-
Germline
-
-
NotI-HindIII
-
-
Raheel Qamar
+/., +?/., -?/.
5
3
c.364G>A
r.(?), r.?
p.(Gly122Arg)
-
likely pathogenic, likely pathogenic (!), likely pathogenic (recessive), pathogenic
g.6331739C>T
g.6428419C>T
c.364G>A, c.364G>A; p.G122R
-
AIPL1_000192
probably rare hypomorphic allele; modulating, but not severely impacting AIPL1 function,
1 more item
Testa 2011,
PubMed: Huang 2018
,
PubMed: Liu-2020
,
PubMed: Sacristan Reviriego 2020
-
-
Germline
-
-
-
-
-
LOVD
+/., +?/., -?/., ?/.
11
3
c.364G>C
r.(?)
p.(Gly122Arg)
-
likely pathogenic, likely pathogenic (!), pathogenic, VUS
g.6331739C>G
g.6428419C>G
AIPL1(NM_014336.4):c.364G>C (p.G122R), c.364G>C, c.364G>C; p.G122R, p.Gly122Arg,
1 more item
-
AIPL1_000038
compound heterozygous missense variant, rare hypomorphic allele, solved, compound heterozygous,
2 more items
PubMed: Jacobson 2011
,
PubMed: Panneman 2023
,
PubMed: Sacristan Reviriego 2020
,
PubMed: Weisschuh 2020
-
-
CLASSIFICATION record, Germline, Unknown
?
-
-
-
-
Raheel Qamar
,
VKGL-NL_Rotterdam
,
Daan Panneman
?/.
2
-
c.383C>T
r.(?)
p.(Ala128Val)
-
VUS
g.6331720G>A
g.6428400G>A
AIPL1(NM_014336.4):c.383C>T (p.A128V), AIPL1(NM_014336.5):c.383C>T (p.A128V)
-
AIPL1_000180
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Rotterdam
,
VKGL-NL_AMC
-/.
3
3
c.390C>A
r.(?)
p.(His130Gln)
-
benign
g.6331713G>T
g.6428393G>T
c.390C>A; p.H130Q
-
AIPL1_000071
homozygous missense variant
Aboshiha 2015,
PubMed: Tan 2012
-
-
Germline, Unknown
-
-
-
-
-
Raheel Qamar
-?/.
1
-
c.392C>A
r.(?)
p.(Thr131Lys)
-
likely benign
g.6331711G>T
-
AIPL1(NM_014336.3):c.392C>A (p.(Thr131Lys))
-
AIPL1_000230
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Leiden
+/., +?/., -?/., ?/.
13
3, 4
c.401A>T
r.(?)
p.(Tyr134Phe)
-
likely benign, likely pathogenic, pathogenic, VUS
g.6331702T>A
g.6428382T>A
c.401A>T, Tyr134Phe,
1 more item
-
AIPL1_000071, AIPL1_000072
homozygous deleterious variant, SNP, VKGL data sharing initiative Nederland
PubMed: Dharmaraj 2004
,
PubMed: Eisenberger-2013
,
PubMed: Vallespin 2007Â
-
rs16955851
CLASSIFICATION record, Germline, Unknown
-
0.01
-
-
-
Raheel Qamar
,
VKGL-NL_Leiden
,
VKGL-NL_Rotterdam
,
VKGL-NL_Groningen
+?/.
2
-
c.404dup
r.(?)
p.(Asp136Glyfs*22)
-
likely pathogenic, likely pathogenic (recessive)
g.6331699dup
g.6428379dup
404_405insA, AIPL1 c.404dup p.(Asp136Glyfs *22)
-
AIPL1_000189
heterozygous
PubMed: Bryant 2018
,
PubMed: Méjécase 2020
-
-
Germline, Unknown
?
-
-
-
-
LOVD
+?/.
1
-
c.406G>T
r.(?)
p.(Asp136Tyr)
ACMG
likely pathogenic
g.6331697C>A
g.6428377C>A
AIPL1 NM_014336: g.6823G>T, c.406G>T, p.D136Y
-
AIPL1_000206
-
PubMed: Xu 2020
-
-
Germline
yes
-
-
-
-
LOVD
-?/.
1
-
c.420G>A
r.(?)
p.(Leu140=)
-
likely benign
g.6331683C>T
g.6428363C>T
AIPL1(NM_014336.4):c.420G>A (p.L140=)
-
AIPL1_000183
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Rotterdam
+/., +?/., ?/.
26
3, 4
c.421C>T
r.(?)
p.(Gln141*), p.(Gln141Ter)
ACMG
likely pathogenic, likely pathogenic (recessive), pathogenic, pathogenic (recessive), VUS
g.6331682G>A
g.6428362G>A
AIPL1 NM_014336: g.6838C>T, c.421C>T, p.Q141X, c.421C>T, c.C241T p.Q81X, c.C241T:p.Gln81*,
1 more item
-
AIPL1_000191
-
PubMed: Huang 2015
,
PubMed: Huang 2018
,
PubMed: Liu-2020
,
PubMed: Wan 2019
,
PubMed: Wang 2015
,
4 more items
-
rs200125117
Germline
?, yes
Whole exome sequencing (WES)
-
-
-
Didem Yücel Yılmaz
-?/.
2
3
c.439C>T
r.(?)
p.(=)
-
likely benign
g.6331664G>A
g.6428344G>A
-
-
AIPL1_000072
homozygous SNP
PubMed: Tan 2012
-
-
Unknown
-
-
-
-
-
Raheel Qamar
+/., ?/.
4
3, 4
c.465G>T
r.(?), r.spl, r.spl?
p.(Gln155His)
ACMG
pathogenic, VUS
g.6331638C>A
g.6428318C>A
AIPL1 c.465G>T, p.(Gln155His), splice mutation c.834G>A, p.(Trp278*),
1 more item
-
AIPL1_000159
-
PubMed: Jespersgaar 2019
,
PubMed: Li 2014
,
PubMed: Li 2017
-
-
Germline
?, yes
-
-
-
-
James Hejtmancik
-?/.
2
3i
c.466-26T>C
r.(?)
p.(=)
-
likely benign
g.6330403A>G
g.6427083A>G
-
-
AIPL1_000156
homozygous SNP
PubMed: Tan 2012
-
rs925615
Unknown
-
-
-
-
-
Raheel Qamar
-/.
1
3i
c.466-25T>C
r.(?)
p.(=)
-
benign
g.6330402A>G
-
IVS3+25 T>C
-
AIPL1_000074
1 more item
PubMed: Sohocki 2000
-
-
Germline
-
-
-
-
-
Raheel Qamar
-?/.
2
3i
c.466-2A>G
r.spl
p.?
-
likely benign
g.6330379T>C
g.6427059T>C
-
-
AIPL1_000154
homozygous missense variant
PubMed: Tan 2012
-
-
Unknown
-
-
-
-
-
Raheel Qamar
?/.
1
-
c.479_482del
r.(?)
p.(Ser160IlefsTer9)
-
VUS
g.6330363_6330366del
-
AIPL1(NM_014336.3):c.479_482delGTGA (p.(Ser160fs))
-
AIPL1_000174
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Leiden
+/., +?/., ?/.
19
3, 4
c.487C>T
r.(?), r.?
p.(Gln163*)
-
likely pathogenic, pathogenic, VUS
g.6330356G>A
g.6427036G>A
487C>T (CAG>TAG), c.487C>T, Gln163X, p.Gln163Ter, Q163X
-
AIPL1_000066
homozygous, homozygous deleterious variant, homozygous SNP, homozygous nonsense variant, {CV:99804}
PubMed: Dharmaraj 2004
,
PubMed: Sohocki 2000
,
PubMed: Tan 2012
,
PubMed: Wang-2013
,
1 more item
-
rs62637009
Germline, Unknown
yes
0.007 in 153 patients; 0 in 96 controls
-
-
-
Raheel Qamar
,
Mahmoud Koko
-?/.
2
3
c.496A>T
r.(?)
p.(Thr166Ser)
-
likely benign
g.6330347T>A
g.6427027T>A
Tyr134Phe
-
AIPL1_000063
homozygous SNP
PubMed: Tan 2012
-
rs16955851
Unknown
-
-
-
-
-
Raheel Qamar
-/., -?/.
6
4
c.516T>C
r.(?)
p.(=), p.(His172=)
-
benign, likely benign
g.6330327A>G
g.6427007A>G
AF148864:516T>C (CAT?CAC) His172His, CAT> CAC (His172His),
1 more item
-
AIPL1_000064
polymorphisms silent substitution, VKGL data sharing initiative Nederland
PubMed: Sohocki 2000
,
PubMed: Sohocki 2001
-
-
CLASSIFICATION record, Germline
-
-
-
-
-
Julia Lopez
,
Raheel Qamar
,
VKGL-NL_Rotterdam
,
VKGL-NL_Nijmegen
,
VKGL-NL_AMC
-?/.
1
-
c.530C>T
r.(?)
p.(Ala177Val)
-
likely benign
g.6330313G>A
-
AIPL1(NM_001285402.2):c.413C>T (p.A138V)
-
AIPL1_000226
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_AMC
+/.
3
4
c.547G>T
r.(?), r.?
p.(Gly183*)
-
pathogenic
g.6330296C>A
g.6426976C>A
c.547G>T
-
AIPL1_000188
-
PubMed: Wang-2013
,
PubMed: Zenteno 2020
-
-
Germline, Unknown
-
1/143 cases
-
-
-
Johan den Dunnen
-?/.
1
-
c.552G>A
r.(?)
p.(Glu184=)
-
likely benign
g.6330291C>T
-
AIPL1(NM_014336.5):c.552G>A (p.E184=)
-
AIPL1_000222
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_AMC
?/.
1
-
c.553G>A
r.(?)
p.(Gly185Arg)
ACMG
VUS
g.6330290C>T
g.6426970C>T
AIPL1 c.553G>A, p.(Gly185Arg)
-
AIPL1_000223
compound heterozygous, probably causal
PubMed: Zhu 2022
-
-
Germline/De novo (untested)
?
-
-
-
-
LOVD
-?/.
2
4
c.555A>G
r.(?)
p.(=)
-
likely benign
g.6330288T>C
g.6426968T>C
-
-
AIPL1_000059
homozygous missense variant
PubMed: Tan 2012
-
-
Unknown
-
-
-
-
-
Raheel Qamar
?/.
1
-
c.562C>T
r.(?)
p.(Leu188Phe)
-
VUS
g.6330281G>A
-
-
-
AIPL1_000220
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Nijmegen
?/.
1
-
c.572T>C
r.(?)
p.(Leu191Pro)
-
VUS
g.6330271A>G
g.6426951A>G
-
-
AIPL1_000194
-
PubMed: Wang 2015
-
-
Germline
-
-
-
-
-
LOVD
+/.
2
5
c.582C>G
r.(?)
p.(Tyr194*)
-
pathogenic
g.6330261G>C
-
c.582C>G, c.582C>G; p.Y194X
-
AIPL1_000216
-
Aboshiha 2015, Kumaran 2018
-
-
Germline
-
-
-
-
-
LOVD
+/., ?/.
14
4
c.589G>C
r.(?)
p.(Ala197Pro)
-
pathogenic, VUS
g.6330254C>G
g.6426934C>G
589G>C (GCC>CCC), Ala197Pro
-
AIPL1_000060
homozygous, homozygous deleterious variant, homozygous missense variant
PubMed: Dharmaraj 2004
,
PubMed: Hanein 2004
,
PubMed: Sohocki 2000
-
-
Germline
-
-
-
-
-
Raheel Qamar
-/.
2
4
c.592T>A
r.(?)
p.(Ser198Thr)
-
benign
g.6330251A>T
g.6426931A>T
-
-
AIPL1_000057
homozygous missense variant, homozygous neutral missense variant
PubMed: Tan 2012
-
-
Unknown
-
-
-
-
-
Raheel Qamar
+/., -?/.
3
4, 5
c.593C>T
r.(?)
p.(Ser198Phe)
-
likely benign, pathogenic
g.6330250G>A
g.6426930G>A
c.593C>T; p.S198F
-
AIPL1_000054
homozygous missense variant
Aboshiha 2015,
PubMed: Tan 2012
-
-
Germline, Unknown
-
-
-
-
-
Raheel Qamar
+/.
2
4
c.613_622del
r.(?)
p.(Ile205*)
-
pathogenic
g.6330224_6330233del
g.6426904_6426913del
613_622delATCATCTGCC
-
AIPL1_000011
-
-
-
-
Germline
yes
8/222
-
-
-
Soumittra Nagasamy
+/.
1
4
c.613_622delATCATCTGC
r.(?)
p.(Ile205Ter)
-
pathogenic (recessive)
g.6330224_6330233del
g.6426904_6426913del
613_622delATCATCTGCC
-
AIPL1_000011
-
PubMed: Srilekha 2015
-
-
Germline
-
-
-
-
-
LOVD
-?/.
1
5
c.616A>G
r.(?)
p.(Ile206Val)
-
likely benign
g.6330227T>C
-
c.616A>G
-
AIPL1_000200
-
PubMed: Chen-2013
-
-
Unknown
-
-
-
-
-
LOVD
+/.
1
5
c.617T>A
r.(?)
p.(Ile206Asn)
-
pathogenic
g.6330226A>T
-
c.617T>A; p.I206N
-
AIPL1_000215
-
Li 2013
-
-
Germline
-
-
-
-
-
LOVD
-/., -?/.
2
-
c.627G>A
r.(?)
p.(Arg209=)
-
benign, likely benign
g.6330216C>T
g.6426896C>T
AIPL1(NM_014336.4):c.627G>A (p.R209=), AIPL1(NM_014336.5):c.627G>A (p.R209=)
-
AIPL1_000167
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Rotterdam
,
VKGL-NL_AMC
-?/.
2
4
c.641A>G
r.(?)
p.(Lys214Arg)
-
likely benign
g.6330202T>C
g.6426882T>C
-
-
AIPL1_000056
homozygous neutral missense variant
PubMed: Tan 2012
-
-
Unknown
-
-
-
-
-
Raheel Qamar
+/.
3
4
c.642G>C
r.(?)
p.(Lys214Asn)
ACMG
pathogenic
g.6330201C>G
g.6426881C>G
AIPL1 NM_014336: g.8319G>C, c.642G>C, p.K214N, Lys214Asn
-
AIPL1_000020
compound heterozygous missense variant
PubMed: Pennesi 2011
,
PubMed: Xu 2020
-
-
Germline
yes
-
-
-
-
Raheel Qamar
+?/.
2
5
c.642G>Y
r.(?)
p.(Lys214Asn)
-
likely pathogenic
g.6330201C>G
-
p.Lys214Asn
-
AIPL1_000020
-
PubMed: Pennesi 2011
-
-
Germline
-
-
-
-
-
LOVD
-/.
1
-
c.642+14G>A
r.(=)
p.(=)
-
benign
g.6330187C>T
g.6426867C>T
AIPL1(NM_014336.5):c.642+14G>A
-
AIPL1_000179
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_AMC
-?/.
2
4i
c.642+33C>T
r.(?)
p.(=)
-
likely benign
g.6330168G>A
g.6426848G>A
642-33C>T, 643-33C>T
-
AIPL1_000043
homozygous SNP
PubMed: Tan 2012
-
rs2292545
Unknown
-
-
-
-
-
Raheel Qamar
-?/.
2
4i
c.642+48G>A
r.(?)
p.(=)
-
likely benign
g.6330153C>T
g.6426833C>T
-
-
AIPL1_000052
homozygous SNP
PubMed: Tan 2012
-
rs925616
Unknown
-
-
-
-
-
Raheel Qamar
-/., -?/.
6
5
c.651A>G
r.(?)
p.(=), p.(Pro217=)
-
benign, likely benign
g.6330068T>C
g.6426748T>C
AIPL1(NM_014336.5):c.651A>G (p.P217=), CCG>CCA (Pro217Pro)
-
AIPL1_000044
homozygous SNP, polymorphisms silent substitution, VKGL data sharing initiative Nederland
PubMed: Sohocki 2000
,
PubMed: Tan 2012
-
rs2292546
CLASSIFICATION record, Germline, Unknown
-
-
-
-
-
Raheel Qamar
,
VKGL-NL_Groningen
,
VKGL-NL_Nijmegen
-?/.
1
-
c.658G>A
r.(?)
p.(Val220Met)
-
likely benign
g.6330061C>T
-
-
-
AIPL1_000231
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Nijmegen
+/.
2
5
c.666G>A
r.(=), r.(?)
p.(=), p.(Trp222*)
-
pathogenic
g.6330053C>T
-
c.666G>A, c.666G>A; p.W222X
-
AIPL1_000214
-
PubMed: Sacristan Reviriego 2020
-
-
Germline
no
-
-
-
-
LOVD
-?/.
2
5
c.678G>A
r.(?)
p.(=)
-
likely benign
g.6330041C>T
g.6426721C>T
678G>A (Glu226Glu
-
AIPL1_000045
homozygous missense variant
PubMed: Tan 2012
-
-
Unknown
-
-
-
-
-
Raheel Qamar
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