Variant #0000000121 (NC_000002.11:g.47657016T>A, NM_000251.2:c.1212T>A (MSH2))

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.47657016T>A
Reference -
DB-ID MSH2_000004
Frequency -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2022-02-14 15:11:57 +00:00 (UTC)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MSH2 NM_000251.2 ?/+ 7 c.1212T>A r.(?) p.(Cys404*)