Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.36996710G>ACA008419MLH1c.207+1G>A (p.=)
c.-83+1G>A (p.=)
c.-517+1G>A (p.=)
c.-425+1G>A (p.=)
c.-517+3047G>A (p.=)
c.-662+1G>A (p.=)
c.-723+1G>A (p.=)
c.-620+1G>A (p.=)
c.-83+1G>A
c.-517+1G>A
c.-425+1G>A
c.-662+1G>A
c.-420+1G>A (p.=)
c.-610+1G>A (p.=)
c.-723+2820G>A (p.=)
c.-523+1G>A (p.=)
c.207+1G>A
c.*287+1G>A (p.=)
c.116+3047G>A (p.=)
c.*85+1G>A (p.=)
n.182+1G>A
n.134+1G>A
n.329+1G>A
n.211+1G>A
n.230+1G>A
ClinVar dbSNP COSMIC
3g.36996710G>TCA008427MLH1c.207+1G>T (p.=)
c.-83+1G>T (p.=)
c.-517+1G>T (p.=)
c.-425+1G>T (p.=)
c.-517+3047G>T (p.=)
c.-662+1G>T (p.=)
c.-723+1G>T (p.=)
c.-620+1G>T (p.=)
c.-83+1G>T
c.-517+1G>T
c.-425+1G>T
c.-662+1G>T
c.-420+1G>T (p.=)
c.-610+1G>T (p.=)
c.-723+2820G>T (p.=)
c.-523+1G>T (p.=)
c.207+1G>T
c.*287+1G>T (p.=)
c.116+3047G>T (p.=)
c.*85+1G>T (p.=)
n.182+1G>T
n.134+1G>T
n.329+1G>T
n.211+1G>T
n.230+1G>T
ClinVar dbSNP

Number of alleles fetched