Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.49621961dup | CA486349772 | MGAT2 | c.693dup (p.His232ThrfsTer?) | COSMIC |
14 | g.49621961A>C | CA389619941 | MGAT2 | c.693A>C (p.Lys231Asn) | |
14 | g.49621961A>G | CA486349775 | MGAT2 | c.693A>G (p.Lys231=) | |
14 | g.49621961A>T | CA389619942 | MGAT2 | c.693A>T (p.Lys231Asn) | |
14 | g.49621962C>A | CA389619948 | MGAT2 | c.694C>A (p.His232Asn) | |
14 | g.49621962C>G | CA389619944 | MGAT2 | c.694C>G (p.His232Asp) | |
14 | g.49621962C>T | CA389619945 | MGAT2 | c.694C>T (p.His232Tyr) | gnomAD v3 gnomAD v4 |
14 | g.49621963A= | CA2135804758 | MGAT2 | c.695A= (p.His232=) | |
14 | g.49621963A>C | CA389619950 | MGAT2 | c.695A>C (p.His232Pro) | COSMIC |
14 | g.49621963A>G | CA389619952 | MGAT2 | c.695A>G (p.His232Arg) | dbSNP gnomAD v2 |
14 | g.49621963A>T | CA389619953 | MGAT2 | c.695A>T (p.His232Leu) | |
14 | g.49621964T>A | CA389619954 | MGAT2 | c.696T>A (p.His232Gln) | |
14 | g.49621964T>C | CA486349779 | MGAT2 | c.696T>C (p.His232=) | |
14 | g.49621964T>G | CA389619956 | MGAT2 | c.696T>G (p.His232Gln) | |
14 | g.49621965C>A | CA389619958 | MGAT2 | c.697C>A (p.His233Asn) | |
14 | g.49621965C>G | CA389619963 | MGAT2 | c.697C>G (p.His233Asp) | |
14 | g.49621965C>T | CA389619960 | MGAT2 | c.697C>T (p.His233Tyr) | |
14 | g.49621966A= | CA2135804759 | MGAT2 | c.698A= (p.His233=) | |
14 | g.49621966A>C | CA389619965 | MGAT2 | c.698A>C (p.His233Pro) | |
14 | g.49621966A>G | CA260660763 | MGAT2 | c.698A>G (p.His233Arg) | dbSNP gnomAD v3 gnomAD v4 |
14 | g.49621966A>T | CA389619969 | MGAT2 | c.698A>T (p.His233Leu) | |
14 | g.49621967C>A | CA389619972 | MGAT2 | c.699C>A (p.His233Gln) | |
14 | g.49621967C>G | CA389619973 | MGAT2 | c.699C>G (p.His233Gln) | |
14 | g.49621967C>T | CA486349783 | MGAT2 | c.699C>T (p.His233=) | gnomAD v4 |
14 | g.49621968T>A | CA389619976 | MGAT2 | c.700T>A (p.Trp234Arg) | |
14 | g.49621968T>C | CA389619979 | MGAT2 | c.700T>C (p.Trp234Arg) | |
14 | g.49621968T>G | CA389619980 | MGAT2 | c.700T>G (p.Trp234Gly) | |
14 | g.49621969G>A | CA389619982 | MGAT2 | c.701G>A (p.Trp234Ter) | gnomAD v4 |
14 | g.49621969G>C | CA389619984 | MGAT2 | c.701G>C (p.Trp234Ser) | |
14 | g.49621969G>T | CA389619986 | MGAT2 | c.701G>T (p.Trp234Leu) | |
14 | g.49621970G>A | CA389619990 | MGAT2 | c.702G>A (p.Trp234Ter) | |
14 | g.49621970G>C | CA389619991 | MGAT2 | c.702G>C (p.Trp234Cys) | |
14 | g.49621970G>T | CA389619988 | MGAT2 | c.702G>T (p.Trp234Cys) | |
14 | g.49621971T>A | CA389619996 | MGAT2 | c.703T>A (p.Trp235Arg) | |
14 | g.49621971T>C | CA389619993 | MGAT2 | c.703T>C (p.Trp235Arg) | |
14 | g.49621971T>G | CA389619995 | MGAT2 | c.703T>G (p.Trp235Gly) | |
14 | g.49621972G>A | CA389619998 | MGAT2 | c.704G>A (p.Trp235Ter) | COSMIC |
14 | g.49621972G>C | CA389620000 | MGAT2 | c.704G>C (p.Trp235Ser) | |
14 | g.49621972G>T | CA389620003 | MGAT2 | c.704G>T (p.Trp235Leu) | |
14 | g.49621973G>A | CA389620013 | MGAT2 | c.705G>A (p.Trp235Ter) | |
14 | g.49621973G>C | CA389620010 | MGAT2 | c.705G>C (p.Trp235Cys) | |
14 | g.49621973G>T | CA389620008 | MGAT2 | c.705G>T (p.Trp235Cys) | |
14 | g.49621974T>A | CA389620015 | MGAT2 | c.706T>A (p.Trp236Arg) | |
14 | g.49621974T>C | CA389620017 | MGAT2 | c.706T>C (p.Trp236Arg) | |
14 | g.49621974T>G | CA389620018 | MGAT2 | c.706T>G (p.Trp236Gly) | |
14 | g.49621975G>A | CA389620020 | MGAT2 | c.707G>A (p.Trp236Ter) | |
14 | g.49621975G>C | CA389620022 | MGAT2 | c.707G>C (p.Trp236Ser) | |
14 | g.49621975G>T | CA389620024 | MGAT2 | c.707G>T (p.Trp236Leu) | |
14 | g.49621976G>A | CA389620026 | MGAT2 | c.708G>A (p.Trp236Ter) | |
14 | g.49621976G>C | CA389620035 | MGAT2 | c.708G>C (p.Trp236Cys) |