Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.36993549T>GCA009606MLH1c.2T>G
c.-631T>G (p.=)
c.-717T>G (p.=)
c.-515T>G
c.-944T>G
c.-857T>G
c.-1094T>G
c.-625T>G (p.=)
c.-949T>G (p.=)
c.-1073T>G (p.=)
c.-283T>G (p.=)
c.-1042T>G (p.=)
c.-1155T>G (p.=)
c.-1064T>G (p.=)
c.-825T>G (p.=)
c.-723T>G (p.=)
c.-820T>G (p.=)
c.-1052T>G (p.=)
c.-810T>G (p.=)
ClinVar dbSNP
3g.36993549T>ACA009594MLH1c.2T>A
c.-631T>A (p.=)
c.-717T>A (p.=)
c.-515T>A
c.-944T>A
c.-857T>A
c.-1094T>A
c.-625T>A (p.=)
c.-949T>A (p.=)
c.-1073T>A (p.=)
c.-283T>A (p.=)
c.-1042T>A (p.=)
c.-1155T>A (p.=)
c.-1064T>A (p.=)
c.-825T>A (p.=)
c.-723T>A (p.=)
c.-820T>A (p.=)
c.-1052T>A (p.=)
c.-810T>A (p.=)
ClinVar dbSNP
3g.36993549T>CCA009600MLH1c.2T>C
c.-631T>C (p.=)
c.-717T>C (p.=)
c.-515T>C
c.-944T>C
c.-857T>C
c.-1094T>C
c.-625T>C (p.=)
c.-949T>C (p.=)
c.-1073T>C (p.=)
c.-283T>C (p.=)
c.-1042T>C (p.=)
c.-1155T>C (p.=)
c.-1064T>C (p.=)
c.-825T>C (p.=)
c.-723T>C (p.=)
c.-820T>C (p.=)
c.-1052T>C (p.=)
c.-810T>C (p.=)
ClinVar dbSNP gnomAD

Number of alleles fetched