Variant #0000274444 (NC_000011.9:g.111781050C>A, NC_000011.9(NM_001885.1):c.324+1G>T (CRYAB))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.111781050C>A
DNA change (hg38) g.111910326C>A
Published as CRYAB(NM_001885.2):c.324+1G>T
ISCN -
DB-ID CRYAB_000037
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-01 14:27:16 +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.-2504C>A r.(?) p.(=)
CRYAB NM_001885.1 +?/. - c.324+1G>T r.spl? p.?


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