Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.47410337G>ACA021573MSH2c.610G>A (p.Gly204Arg)
c.412G>A (p.Gly138Arg)
n.682G>A
n.672G>A
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.47410337G>CCA346731092MSH2c.610G>C (p.Gly204Arg)
c.412G>C (p.Gly138Arg)
n.682G>C
n.672G>C
ClinVar dbSNP
2g.47410337G>TCA021582MSH2c.610G>T (p.Gly204Ter)
c.412G>T (p.Gly138Ter)
n.682G>T
n.672G>T
ClinVar dbSNP

Number of alleles fetched