Variant #0000000666 (NC_000002.11:g.47635675_47635678del, NM_000251.2:c.347_350del (MSH2))

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.47635675_47635678del
Reference -
DB-ID MSH2_000009
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 2025-10-06 06:10:02 +00:00 (UTC)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Class     
MSH2 NM_000251.2 +/+ 2 c.347_350del r.(?) p.(Asp116Glyfs*57) pathogenic