Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.47414381T>CCA10577960MSH2c.905T>C (p.Leu302Ser)
c.707T>C (p.Leu236Ser)
n.977T>C
n.967T>C
 ClinVar dbSNP gnomAD v3 gnomAD v4
2g.47414381T>ACA022523MSH2c.905T>A (p.Leu302Ter)
c.707T>A (p.Leu236Ter)
n.977T>A
n.967T>A
 ClinVar dbSNP

Number of alleles fetched