Variant #0000229361 (NC_000002.11:g.47639507del, NC_000002.11(NM_000251.2):c.646-46del (MSH2))

Chromosome 2
DNA change (genomic) (Relative to hg19 / GRCh37) g.47639507del
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID MSH2_000042
Frequency 10/12340
Freq. EA 10/8180
Freq. AA 0/4160
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 22:20:38 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
MSH2 NM_000251.2 ?/? c.646-46del r.(=) p.(=)