Variant #0000936230 (NC_000009.11:g.128000392C>T, NC_000009.11(NM_005347.4):c.1402+28G>A (HSPA5))

Chromosome 9
DNA change (genomic) (Relative to hg19 / GRCh37) g.128000392C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID HSPA5_000022
Frequency 5/13006
Freq. EA 4/8600
Freq. AA 1/4406
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 17:43:11 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
HSPA5 NM_005347.4 ?/? c.1402+28G>A r.(=) p.(=)