Variant #0000613027 (NC_000011.9:g.111782297G>A, NM_001885.1:c.152C>T (CRYAB))

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.111782297G>A
DNA change (hg38) g.111911573G>A
Published as CRYAB(NM_001885.2):c.152C>T (p.P51L), CRYAB(NM_001885.3):c.152C>T (p.P51L)
ISCN -
DB-ID CRYAB_000009 See all 6 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00056 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HSPB2 NM_001541.3 -/. - c.-1257G>A r.(?) p.(=)
CRYAB NM_001885.1 -/. - c.152C>T r.(?) p.(Pro51Leu)


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