Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.36993668G>ACA027435MLH1c.116+5G>A (p.=)
c.121G>A (p.Gly41Arg)
n.91+5G>A
c.-517+5G>A (p.=)
c.-603+5G>A (p.=)
c.-396G>A
c.-825G>A
c.-738G>A
c.-975G>A
c.-511+5G>A (p.=)
c.-830G>A (p.=)
c.-954G>A (p.=)
c.-169+5G>A (p.=)
c.-923G>A (p.=)
c.-1036G>A (p.=)
c.-945G>A (p.=)
c.-711+5G>A (p.=)
c.-609+5G>A (p.=)
c.-706+5G>A (p.=)
c.-933G>A (p.=)
c.116+5G>A
c.-696+5G>A (p.=)
ClinVar dbSNP ExAC gnomAD
3g.36993668G>CCA004556MLH1c.116+5G>C (p.=)
c.121G>C (p.Gly41Arg)
n.91+5G>C
c.-517+5G>C (p.=)
c.-603+5G>C (p.=)
c.-396G>C
c.-825G>C
c.-738G>C
c.-975G>C
c.-511+5G>C (p.=)
c.-830G>C (p.=)
c.-954G>C (p.=)
c.-169+5G>C (p.=)
c.-923G>C (p.=)
c.-1036G>C (p.=)
c.-945G>C (p.=)
c.-711+5G>C (p.=)
c.-609+5G>C (p.=)
c.-706+5G>C (p.=)
c.-933G>C (p.=)
c.116+5G>C
c.-696+5G>C (p.=)
ClinVar dbSNP

Number of alleles fetched