Variant #0000542338 (NC_000011.9:g.111782256G>T, NM_001885.1:c.193C>A (CRYAB))

Chromosome 11
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.111782256G>T
DNA change (hg38) g.111911532G>T
Published as CRYAB(NM_001885.3):c.193C>A (p.L65I)
ISCN -
DB-ID CRYAB_000048
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) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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.-1298G>T r.(?) p.(=)
CRYAB NM_001885.1 ?/. - c.193C>A r.(?) p.(Leu65Ile)


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