Variant #0000000343 (NC_000002.11:g.48025785A>C, MSH6(NM_000179.2):c.663A>C)

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.48025785A>C
Reference -
DB-ID MSH6_000009
Frequency -
Average frequency (gnomAD v.2.1.1) 0.0007 View details
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MSH6 NM_000179.2 ?/? 4 c.663A>C r.(?) p.(Glu221Asp)