Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.47476361T>CCA019764MSH2c.2006-6T>C (p.=)
c.1808-6T>C (p.=)
n.2078-6T>C
n.2068-6T>C
c.*402-6T>C (p.=)
c.*546-6T>C (p.=)
c.*772-6T>C (p.=)
c.*978-6T>C (p.=)
ClinVar dbSNP ExAC gnomAD
2g.47476361T>GCA019771MSH2c.2006-6T>G (p.=)
c.1808-6T>G (p.=)
n.2078-6T>G
n.2068-6T>G
c.*402-6T>G (p.=)
c.*546-6T>G (p.=)
c.*772-6T>G (p.=)
c.*978-6T>G (p.=)
ClinVar dbSNP
2g.47476361T>ACA46702149MSH2c.2006-6T>A (p.=)
c.1808-6T>A (p.=)
n.2078-6T>A
n.2068-6T>A
c.*402-6T>A (p.=)
c.*546-6T>A (p.=)
c.*772-6T>A (p.=)
c.*978-6T>A (p.=)
dbSNP gnomAD

Number of alleles fetched