Variant #0000936262 (NC_000009.11:g.128002431A>G, NC_000009.11(NM_005347.4):c.492+20T>C (HSPA5))

Chromosome 9
DNA change (genomic) (Relative to hg19 / GRCh37) g.128002431A>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID HSPA5_000054
Frequency 1/12998
Freq. EA 0/8596
Freq. AA 1/4402
Average frequency (gnomAD v.2.1.1) -
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Ivo F.A.C. Fokkema
Date created 2013-05-03 16:29:58 +02:00 (CEST)
Date last edited 2013-05-04 17:43:13 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
HSPA5 NM_005347.4 ?/? c.492+20T>C r.(=) p.(=)