Variant #0000229396 (NC_000002.11:g.47656874A>G, NC_000002.11(NM_000251.2):c.1077-7A>G (MSH2))

Chromosome 2
DNA change (genomic) (Relative to hg19 / GRCh37) g.47656874A>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID MSH2_000082
Frequency 3/12906
Freq. EA 0/8578
Freq. AA 3/4328
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 16:22:05 +02:00 (CEST)
Date last edited 2013-05-03 22:20:43 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
MSH2 NM_000251.2 ?/? c.1077-7A>G r.(=) p.(=)