Variant #0000229607 (NC_000002.11:g.48026308C>G, NM_000179.2:c.1186C>G (MSH6))

Chromosome 2
DNA change (genomic) (Relative to hg19 / GRCh37) g.48026308C>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID MSH6_000073
Frequency 60/13006
Freq. EA 56/8600
Freq. AA 4/4406
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 22:21:06 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
MSH6 NM_000179.2 ?/? c.1186C>G r.(?) p.(Leu396Val)