Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.6003689C>TCA10577352PMS2c.353+1G>A (p.=)
c.-53+1G>A (p.=)
n.35+283G>A (p.=)
n.432+1G>A
n.353+1G>A (p.=)
n.353+1G>A
n.545G>A
c.35+283G>A (p.=)
n.62+2304G>A
n.435+1G>A
c.347+1G>A (p.=)
c.398+1G>A (p.=)
c.-532+1G>A (p.=)
c.-132+1G>A (p.=)
n.440+1G>A
c.-432+1G>A (p.=)
ClinVar dbSNP
7g.6003689C>ACA153247782PMS2c.353+1G>T (p.=)
c.-53+1G>T (p.=)
n.35+283G>T (p.=)
n.432+1G>T
n.353+1G>T (p.=)
n.353+1G>T
n.545G>T
c.35+283G>T (p.=)
n.62+2304G>T
n.435+1G>T
c.347+1G>T (p.=)
c.398+1G>T (p.=)
c.-532+1G>T (p.=)
c.-132+1G>T (p.=)
n.440+1G>T
c.-432+1G>T (p.=)
dbSNP

Number of alleles fetched