Global Variome shared LOVD
CRYAA (crystallin, alpha A)
LOVD v.3.0 Build 30b [
Current LOVD status
]
Register as submitter
|
Log in
Curators:
Lars Hansen
and
Johan den Dunnen
View all genes
View CRYAA gene homepage
View graphs about the CRYAA gene database
Create a new gene entry
View all transcripts
View all transcripts of gene CRYAA
Create a new transcript information entry
View all variants
View all variants affecting transcripts
View unique variants in gene CRYAA
View all variants in gene CRYAA
Full data view for gene CRYAA
Create a new data submission
View active genomic custom columns
Enable more genomic custom columns
View all individuals
View all individuals with variants in gene CRYAA
Create a new data submission
View active custom columns
Enable more custom columns
View all diseases
View all diseases associated with gene CRYAA
Create a new disease information entry
View available phenotype columns
View all screenings
View all screenings for gene CRYAA
Create a new data submission
View active custom columns
Enable more custom columns
Submit new data
Unique variants in the CRYAA gene
This database is one of the
"Eye disease"
gene variant databases.
The variants shown are described using the NM_000394.2 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.
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
All list views have search fields which can be used to search data. You can search for a complete word or you can search for a part of a search term. If you enclose two or more words in double quotes, LOVD will search for the combination of those words only exactly in the order you specify. Note that search terms are case-insensitive and that wildcards such as * are treated as normal text! For all options, like "and", "or", and "not" searches, or searching for prefixes or suffixes, see the table below.
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.
42 entries on 1 page. Showing entries 1 - 42.
10 per page
25 per page
50 per page
100 per page
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
-/., -?/., ?/.
17
1
c.6C>T
r.(?)
p.(=), p.(Asp2=)
-
benign, likely benign, VUS
g.44589215C>T
g.43169105C>T
6G>A, 6T>C, D2D
-
CRYAA_000010
10/11 families tested, 144 controls, 910 cataract cases, in controls and cataract patients,
2 more items
PubMed: Beby 2007
,
PubMed: Bhagyalaxmi 2010
,
PubMed: Graw 2006
,
PubMed: Li 2019
,
PubMed: Litt 1998
,
3 more items
-
rs872331
Germline
-
10/11/15, 121/455, 24/144, 28/455, 3/144
-
-
-
Johan den Dunnen
,
Lars Hansen
+/.
2
1
c.27G>A
r.(?)
p.(Trp9*)
-
pathogenic
g.44589236G>A
g.43169126G>A
-
-
CRYAA_000001
not in 140 control chromosomes
PubMed: Pras 2000
,
OMIM:var0002
-
rs74315440
Germline
-
-
HinfI+
-
-
Johan den Dunnen
+/., +?/.
11
1
c.34C>T
r.(?)
p.(Arg12Cys)
ACMG
likely pathogenic, pathogenic, pathogenic (dominant)
g.44589243C>T
g.43169133C>T
104C>T, c.34C-->T; p.Arg12Cys, CRYAA c.34C>T p.(Arg12Cys) het,
1 more item
-
CRYAA_000002
heterozygous, no Sanger sequencing; heterozygous, not in 100 control chromosomes,
2 more items
PubMed: Devi 2008
,
PubMed: Hansen 2007
,
PubMed: Hansen 2009
,
PubMed: Lenassi 2020
,
PubMed: Patel 2019
,
4 more items
-
-
CLASSIFICATION record, Germline
?, yes
-
ApaLI+, HhaI-
-
-
Johan den Dunnen
,
Lars Hansen
,
VKGL-NL_Leiden
,
VKGL-NL_Groningen
,
VKGL-NL_Nijmegen
+?/.
2
1
c.35G>T
r.(?)
p.(Arg12Leu)
ACMG
likely pathogenic, likely pathogenic (dominant)
g.44589244G>T
g.43169134G>T
-
-
CRYAA_000021
ACMG PM1, PM2, PP1, PP2, PP3
PubMed: Zhuang 2019
-
-
Germline
yes
-
-
-
-
Johan den Dunnen
,
Zongfu Cao
+/., +?/.
19
1
c.61C>T
r.(?)
p.(Arg21Trp)
ACMG
likely pathogenic, likely pathogenic (dominant), pathogenic, pathogenic (dominant)
g.44589270C>T
g.43169160C>T
130C>T, CRYAA c.61C>T p.(Arg21Trp) het, CRYAA(NM_000394.4):c.61C>T (p.R21W)
-
CRYAA_000003
ACMG PM1, PM2, PP1, PP2, PP3, PP5, heterozygous, not in 100 control chromosomes,
2 more items
PubMed: Devi 2008
,
PubMed: Fan 2020
,
PubMed: Fernandez-Alcalde 2021
,
PubMed: Hansen 2009
,
9 more items
rs397515625
rs397515625
CLASSIFICATION record, Germline
?, yes
-
MspI-
-
-
Johan den Dunnen
,
Lars Hansen
,
Jamie Zeegers
,
VKGL-NL_Nijmegen
,
VKGL-NL_VUmc
+/.
7
1
c.62G>A
r.(?)
p.(Arg21Gln)
-
pathogenic
g.44589271G>A
g.43169161G>A
-
-
CRYAA_000014
-
PubMed: Javadiyan 2016
,
Journal: Javadiyan 2016
,
PubMed: Laurie 2013
,
Journal: Laurie 2013
-
-
Germline
yes
-
PvuII+
-
-
Kathryn Burdon
,
Jamie Zeegers
+/., +?/.
2
1
c.62G>T
r.(?)
p.(Arg21Leu)
ACMG
likely pathogenic, pathogenic
g.44589271G>T
g.43169161G>T
62C>T, CRYAA c.62G>T p.(Arg21Leu) het
-
CRYAA_000008
heterozygous, not in 192 control chromosomes
PubMed: Graw 2006
,
PubMed: Lenassi 2020
-
-
Germline
?
-
HpaII-
-
-
Johan den Dunnen
+?/.
1
-
c.142T>G
r.(?)
p.(Tyr48Asp)
-
likely pathogenic (dominant)
g.44589351T>G
g.43169241T>G
-
-
CRYAA_000034
-
PubMed: Ma 2016
-
-
Germline
-
-
-
-
-
Johan den Dunnen
+/., +?/.
6
1
c.145C>T
r.(145c>u), r.(?)
p.(Arg49Cys), p.Arg49Cys
-
likely pathogenic (dominant), NA, pathogenic, pathogenic (recessive)
g.44589354C>T
g.43169244C>T
155C>T
-
CRYAA_000004
1 heterozygous, no homozygous;
Clinindb (India)
, mapped by linkage (LOD 3.3),
1 more item
PubMed: Berry 2020
,
PubMed: Hansen 2009
,
PubMed: Mackay 2003
,
PubMed: Mackay 2003
,
OMIM:var0003
,
2 more items
-
rs74315441
Germline, In vitro (cloned)
yes
1/2795 individuals
AciI-
-
-
Johan den Dunnen
,
Lars Hansen
,
Mohammed Faruq
-?/.
1
-
c.154C>T
r.(?)
p.(Leu52Phe)
-
likely benign
g.44589363C>T
-
CRYAA(NM_000394.3):c.154C>T (p.L52F)
-
CRYAA_000023
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Rotterdam
+/.
10
1
c.(160C>T), c.160C>T
r.(?), r.160c>u
p.(Arg54Cys), p.Arg54Cys
ACMG
pathogenic, pathogenic (!), pathogenic (dominant), pathogenic (recessive)
g.44589369C>T
g.43169259C>T
230C>T, mouse
-
CRYAA_000000, CRYAA_000009
incomplete penetrance, nm3365 mouse, spontaneous mutant, not in 100 control chromosomes
PubMed: Devi 2008
,
PubMed: Javadiyan 2017
,
PubMed: Khan 2007
,
PubMed: Khan 2015
,
PubMed: Liu 2023
,
2 more items
rs397515623
rs397515623
Germline
yes
-
HpyCH4V+
-
-
Johan den Dunnen
+/., ?/.
3
1
c.(161G>A), c.161G>A
r.(?)
p.(Arg54His)
-
pathogenic, VUS
g.44589370G>A
g.43169260G>A
CRYAA(NM_000394.3):c.161G>A (p.R54H), mouse
-
CRYAA_000000
lop18 mouse, VKGL data sharing initiative Nederland
PubMed: Chang 1999
-
-
CLASSIFICATION record, Germline
-
-
-
-
-
Johan den Dunnen
,
VKGL-NL_Rotterdam
+/.
5
1
c.161G>C
r.(?)
p.(Arg54Pro)
-
pathogenic, pathogenic (recessive)
g.44589370G>C
g.43169260G>C
-
-
CRYAA_000019
-
PubMed: Dongmei 2012
,
PubMed: Patel 2017
-
-
Germline
yes
-
-
-
-
Johan den Dunnen
,
Jamie Zeegers
?/.
1
-
c.188A>T
r.(?)
p.(Glu63Val)
-
VUS
g.44589397A>T
-
CRYAA(NM_000394.2):c.188A>T (p.(Glu63Val))
-
CRYAA_000039
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Leiden
-/.
1
1i
c.189+11dup
r.(=)
p.(=)
-
benign
g.44589409dup
g.43169299dup
IVS1+10insG
-
CRYAA_000016
-
PubMed: Santhiya 2006
-
-
Germline
-
-
-
-
-
Johan den Dunnen
?/.
1
1i
c.189+57G>A
r.(=)
p.(=)
-
VUS
g.44589455G>A
g.43169345G>A
189+56G>A
-
CRYAA_000012
-
PubMed: Pang 2002
-
-
Germline
-
-
-
-
-
Johan den Dunnen
?/.
1
1i
c.189+171C>T
r.(=)
p.(=)
-
VUS
g.44589569C>T
g.43169459C>T
189+170C>T
-
CRYAA_000011
not in controls
PubMed: Pang 2002
-
rs11700709
Germline
-
-
-
-
-
Johan den Dunnen
-/.
1
1i
c.190-36dup
r.(=)
p.(=)
-
benign
g.44590591dup
g.43170481dup
IVS1-36insC
-
CRYAA_000017
-
PubMed: Santhiya 2006
-
-
Germline
-
-
-
-
-
Johan den Dunnen
+/.
1
-
c.193C>T
r.(?)
p.(Arg65Ter)
-
pathogenic
g.44590630C>T
g.43170520C>T
-
-
CRYAA_000022
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Nijmegen
+/.
3
2
c.213C>A
r.(?)
p.(Phe71Leu), p.Phe71Leu
-
NA, pathogenic
g.44590650C>A
g.43170540C>A
-
-
CRYAA_000015
not in 530 control chromosomes; 3/711 ARC patients, tested in vitro in several assays
PubMed: Bhagyalaxmi 2009
-
-
Germline, In vitro (cloned)
-
3/1422
-
-
-
Johan den Dunnen
-?/.
1
-
c.213C>T
r.(?)
p.(Phe71=)
-
likely benign
g.44590650C>T
-
CRYAA(NM_000394.3):c.213C>T (p.F71=)
-
CRYAA_000024
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Rotterdam
?/.
1
-
c.235C>A
r.(?)
p.(His79Asn)
-
VUS
g.44590672C>A
-
CRYAA(NM_000394.3):c.235C>A (p.H79N)
-
CRYAA_000025
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Rotterdam
+?/.
1
-
c.253C>T
r.(?)
p.(Leu85Phe)
ACMG
likely pathogenic (dominant)
g.44590690C>T
g.43170580C>T
-
-
CRYAA_000036
ACMG PM1, PM2, PP1, PP3
PubMed: Khidiyatova 2023
-
-
Germline
-
-
-
-
-
Johan den Dunnen
+?/.
1
-
c.275A>G
r.(?)
p.(Asp92Gly)
-
likely pathogenic
g.44590712A>G
g.43170602A>G
c.275A-->G; p.Asp92Gly
-
CRYAA_000027
no Sanger sequencing; heterozygous
PubMed: Patel 2019
-
-
Germline
?
-
-
-
-
LOVD
+?/.
2
-
c.291C>G
r.(?)
p.(His97Gln)
ACMG
likely pathogenic (dominant)
g.44590728C>G
g.43170618C>G
-
-
CRYAA_000037
ACMG PM1, PM2, PP2 ,PP3
PubMed: Khidiyatova 2023
-
-
Germline
-
-
-
-
-
Johan den Dunnen
+/.
3
2
c.292G>A
r.(?)
p.(Gly98Arg)
-
pathogenic, pathogenic (dominant)
g.44590729G>A
g.43170619G>A
-
-
CRYAA_000005
not in 252 control chromosomes
PubMed: Santhiya 2006
,
PubMed: Sun 2011
-
-
Germline
yes
-
BstDSI-
-
-
Johan den Dunnen
+?/.
1
-
c.307C>T
r.(?)
p.(Arg103Cys)
-
likely pathogenic
g.44590744C>T
g.43170634C>T
-
-
CRYAA_000026
-
PubMed: Huang 2015
-
-
Germline
-
-
-
-
-
LOVD
-/.
1
2i
c.312+27G>C
r.(?)
p.(=)
-
benign
g.44590776G>C
g.43170666G>C
IVS2+27G>C
-
CRYAA_000018
-
PubMed: Santhiya 2006
-
-
Germline
-
-
-
-
-
Johan den Dunnen
?/.
1
2i
c.312+172G>A
r.(=)
p.(=)
-
VUS
g.44590921G>A
g.43170811G>A
-
-
CRYAA_000013
in controls and cataract patients
PubMed: Pang 2002
-
rs3819160
Germline
-
-
-
-
-
Johan den Dunnen
+?/.
1
-
c.346C>G
r.(?)
p.(Arg116Gly)
-
likely pathogenic
g.44592214C>G
g.43172104C>G
CRYAA c.346C>G, p.(Arg116Gly)
-
CRYAA_000030
heterozygous, present in 3+ affected family members
PubMed: Bell 2021
-
-
Germline
yes
-
-
-
-
LOVD
+/., +?/.
20
1, 3
c.346C>T
r.(?), r.346c>u
p.(Arg116Cys), p.(Arg12Cys), p.Arg116Cys
ACMG
likely pathogenic (dominant), NA, pathogenic, pathogenic (dominant)
g.44589243C>T, g.44592214C>T
g.43169133C>T, g.43172104C>T
413C>T
-
CRYAA_000002, CRYAA_000007
ACMG PM1, PM2, PP1, PP2, PP3, PP5, mapped by linkage (LOD 3.5),
5 more items
PubMed: Beby 2007
,
OMIM:var0001
,
PubMed: Cobb 2000
,
OMIM:var0001
,
PubMed: Fu 2003
,
OMIM:var0001
,
5 more items
rs397515624, rs74315439
rs397515624
,
rs74315439
Germline, In vitro (cloned)
no, yes
-
BtsI+
-
-
Johan den Dunnen
,
Lars Hansen
+/., +?/.
8
3
c.347G>A
r.(?)
p.(Arg116His), p.Arg116His
-
likely pathogenic (dominant), NA, pathogenic, pathogenic (dominant)
g.44592215G>A
g.43172105G>A
337G>A, 346G>A (R116H), G347A, G414A, G414A (R116H)
-
CRYAA_000006
in vitro analysis, mapped by linkage (LOD score 3.763), mapped by linkage (LOD score 4.43),
2 more items
PubMed: Gu 2008
,
PubMed: Hansen 2007
,
PubMed: Hansen 2009
,
PubMed: Kessel 2021
,
PubMed: Pang 2010
,
3 more items
VCV000016960.2
-
Germline, In vitro (cloned)
-
-
HhaI-
-
-
Johan den Dunnen
,
Lars Hansen
?/.
1
-
c.349C>T
r.(?)
p.(Arg117Cys)
-
VUS
g.44592217C>T
g.43172107C>T
-
-
CRYAA_000035
VUS PS4sup, PM2, PP3
PubMed: Kessel 2021
VCV000898794.1
-
Germline
-
-
-
-
-
Johan den Dunnen
+?/.
1
3
c.349_351del
r.(?)
p.(Arg117del)
-
likely pathogenic
g.44592217_44592219del
g.43172107_43172109del
246_248delCGC (117delR)
-
CRYAA_000020
-
PubMed: Kong 2015
,
Journal: Kong 2015
-
-
Germline
yes
-
-
-
-
Jamie Zeegers
+/.
1
-
c.350_352del
r.(?)
p.(Arg117_Tyr118delinsHis)
-
pathogenic (dominant)
g.44592218_44592220del
g.43172108_43172110del
350_352delGCT
-
CRYAA_000038
-
PubMed: Sun 2011
-
-
Germline
yes
-
-
-
-
Johan den Dunnen
+/.
1
3
c.(352T>G)
r.352u>g
p.Tyr118Asp
-
pathogenic
g.44592220T>G
g.43172110T>G
mouse
-
CRYAA_000000
L1N mouse, ENU induced
PubMed: Xia 2006
-
-
Germline
-
-
-
-
-
Johan den Dunnen
-?/., ?/.
2
-
c.356G>A
r.(?)
p.(Arg119His)
-
likely benign, VUS
g.44592224G>A
-
CRYAA(NM_000394.2):c.356G>A (p.(Arg119His)), CRYAA(NM_000394.3):c.356G>A (p.R119H)
-
CRYAA_000028
VKGL data sharing initiative Nederland
-
-
-
CLASSIFICATION record
-
-
-
-
-
VKGL-NL_Leiden
,
VKGL-NL_Rotterdam
+/.
1
3
c.(371T>A)
r.(?)
p.(Val124Gln)
-
pathogenic
g.44592239T>A
g.43172129T>A
mouse
-
CRYAA_000000
Aey7 mouse, ENU induced
PubMed: Graw 2001
-
-
Germline
-
-
-
-
-
Johan den Dunnen
?/.
1
-
c.410G>C
r.(?)
p.(Gly137Ala)
ACMG
VUS
g.44592278G>C
g.43172168G>C
MIP c.559C>T p.(Arg187Cys) het CRYAA c.410G>C p.(Gly137Ala) het
-
CRYAA_000029
compound heterozygous
PubMed: Lenassi 2020
-
-
Germline
?
-
-
-
-
LOVD
+/.
1
-
c.440del
r.(?)
p.(Gln147ArgfsTer48)
ACMG
pathogenic (dominant)
g.44592308del
g.43172198del
440delA
-
CRYAA_000032
-
PubMed: Javadiyan 2017
-
-
Germline
yes
-
-
-
-
Johan den Dunnen
+?/.
1
-
c.454_456del
r.(?)
p.(Ala152del)
-
likely pathogenic (dominant)
g.44592322_44592324del
g.43172212_43172214del
454delGCC
-
CRYAA_000033
-
PubMed: Berry 2020
-
-
Germline/De novo (untested)
-
-
-
-
-
Johan den Dunnen
+/.
1
-
c.481G>A
r.(?)
p.(Val161Met)
-
pathogenic
g.44592349G>A
g.43172239G>A
-
-
CRYAA_000031
-
PubMed: Li 2016
-
-
Germline
-
-
-
-
-
Johan den Dunnen
10 per page
25 per page
50 per page
100 per page
Legend
How to query
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our
APIs
to retrieve data.
Powered by
LOVD v.3.0
Build 30b
LOVD software ©2004-2024
Leiden University Medical Center
Database contents © by their respective submitters and curators