Variant #0000229347 (NC_000002.11:g.47637301T>G, NM_000251.2:c.435T>G (MSH2))

Chromosome 2
DNA change (genomic) (Relative to hg19 / GRCh37) g.47637301T>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID MSH2_000038
Frequency 5/13006
Freq. EA 5/8600
Freq. AA 0/4406
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 16:22:05 +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.435T>G r.(?) p.(Ile145Met)