Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.47466809G>ACA018837MSH2c.1661+1G>A (p.=)
c.1463+1G>A (p.=)
n.1733+1G>A
c.1661+1G>A
n.1723+1G>A
c.*57+1G>A (p.=)
c.*201+1G>A (p.=)
c.*427+1G>A (p.=)
c.*633+1G>A (p.=)
ClinVar dbSNP
2g.47466809G>TCA018841MSH2c.1661+1G>T (p.=)
c.1463+1G>T (p.=)
n.1733+1G>T
c.1661+1G>T
n.1723+1G>T
c.*57+1G>T (p.=)
c.*201+1G>T (p.=)
c.*427+1G>T (p.=)
c.*633+1G>T (p.=)
ClinVar dbSNP COSMIC

Number of alleles fetched