Variant #0000009481 (NC_000002.11:-, MSH2(NM_000251.1):c.295A>C)

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type c.295A>C;p.Arg99Arg
DNA change (genomic) (Relative to hg19 / GRCh37) -
Reference GenBank
DB-ID MSH2_00060
Frequency 0.0833
Variant remarks Exon
ClassClinical -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Qi Ming
Database submission license No license selected
Created by Qi Ming
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MSH2 NM_000251.1 ./. 02 c.295A>C - p.Arg99Arg