Variant #0000435973 (NC_000011.9:g.111779828C>T, NC_000011.9(NM_001885.1):c.325-137G>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.111779828C>T
DNA change (hg38) g.111909104C>T
Published as -
ISCN -
DB-ID CRYAB_000013
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs11214039
Origin Germline
Segregation -
Frequency 0.00-0.08
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00714 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2010-03-14 16:02:14 +01:00 (CET)
Date last edited 2012-11-02 20:40:47 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CRYAB NM_001885.1 ?/. 2i c.325-137G>A r.(?) p.(=)


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