Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.47480872G>ACA020828MSH2c.2634+1G>A (p.=)
c.2436+1G>A (p.=)
n.2706+1G>A
n.2696+1G>A
n.75+1G>A
c.*1030+1G>A (p.=)
c.*1174+1G>A (p.=)
c.*1400+1G>A (p.=)
c.*1606+1G>A (p.=)
c.*200+1G>A (p.=)
ClinVar dbSNP
2g.47480872G>TCA020831MSH2c.2634+1G>T (p.=)
c.2436+1G>T (p.=)
n.2706+1G>T
n.2696+1G>T
n.75+1G>T
c.*1030+1G>T (p.=)
c.*1174+1G>T (p.=)
c.*1400+1G>T (p.=)
c.*1606+1G>T (p.=)
c.*200+1G>T (p.=)
ClinVar dbSNP

Number of alleles fetched