Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.49621931T>A | CA389619778 | MGAT2 | c.663T>A (p.His221Gln) | |
14 | g.49621931T>C | CA486349731 | MGAT2 | c.663T>C (p.His221=) | dbSNP gnomAD v2 gnomAD v4 |
14 | g.49621931T>G | CA389619781 | MGAT2 | c.663T>G (p.His221Gln) | |
14 | g.49621931T= | CA2135804745 | MGAT2 | c.663T= (p.His221=) | |
14 | g.49621932T>A | CA389619782 | MGAT2 | c.664T>A (p.Tyr222Asn) | |
14 | g.49621932T>C | CA389619784 | MGAT2 | c.664T>C (p.Tyr222His) | |
14 | g.49621932T>G | CA389619787 | MGAT2 | c.664T>G (p.Tyr222Asp) | |
14 | g.49621933A>C | CA389619790 | MGAT2 | c.665A>C (p.Tyr222Ser) | |
14 | g.49621933A>G | CA389619793 | MGAT2 | c.665A>G (p.Tyr222Cys) | gnomAD v4 |
14 | g.49621933A>T | CA389619791 | MGAT2 | c.665A>T (p.Tyr222Phe) | |
14 | g.49621934T>A | CA389619795 | MGAT2 | c.666T>A (p.Tyr222Ter) | |
14 | g.49621934T>C | CA260660756 | MGAT2 | c.666T>C (p.Tyr222=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.49621934T>G | CA389619798 | MGAT2 | c.666T>G (p.Tyr222Ter) | |
14 | g.49621934T= | CA2135804746 | MGAT2 | c.666T= (p.Tyr222=) | |
14 | g.49621935A>C | CA486349737 | MGAT2 | c.667A>C (p.Arg223=) | |
14 | g.49621935A>G | CA389619801 | MGAT2 | c.667A>G (p.Arg223Gly) | |
14 | g.49621935A>T | CA389619802 | MGAT2 | c.667A>T (p.Arg223Ter) | |
14 | g.49621939_49621940del | CA2624726677 | MGAT2 | c.671_672del (p.Glu224GlyfsTer?) | gnomAD v4 |
14 | g.49621936G>A | CA389619804 | MGAT2 | c.668G>A (p.Arg223Lys) | |
14 | g.49621936G>C | CA389619807 | MGAT2 | c.668G>C (p.Arg223Thr) | |
14 | g.49621936G>T | CA389619809 | MGAT2 | c.668G>T (p.Arg223Ile) | |
14 | g.49621937A>C | CA389619812 | MGAT2 | c.669A>C (p.Arg223Ser) | |
14 | g.49621937A>G | CA486349738 | MGAT2 | c.669A>G (p.Arg223=) | |
14 | g.49621937A>T | CA389619813 | MGAT2 | c.669A>T (p.Arg223Ser) | |
14 | g.49621938G>A | CA389619816 | MGAT2 | c.670G>A (p.Glu224Lys) | |
14 | g.49621938G>C | CA389619818 | MGAT2 | c.670G>C (p.Glu224Gln) | |
14 | g.49621938G>T | CA389619820 | MGAT2 | c.670G>T (p.Glu224Ter) | |
14 | g.49621939A= | CA2135804747 | MGAT2 | c.671A= (p.Glu224=) | |
14 | g.49621939A>C | CA389619828 | MGAT2 | c.671A>C (p.Glu224Ala) | |
14 | g.49621939A>G | CA389619822 | MGAT2 | c.671A>G (p.Glu224Gly) | dbSNP gnomAD v3 gnomAD v4 |
14 | g.49621939A>T | CA389619824 | MGAT2 | c.671A>T (p.Glu224Val) | |
14 | g.49621940G>A | CA486349742 | MGAT2 | c.672G>A (p.Glu224=) | dbSNP gnomAD v4 |
14 | g.49621940G>C | CA389619830 | MGAT2 | c.672G>C (p.Glu224Asp) | |
14 | g.49621940G= | CA2135804748 | MGAT2 | c.672G= (p.Glu224=) | |
14 | g.49621940G>T | CA389619832 | MGAT2 | c.672G>T (p.Glu224Asp) | |
14 | g.49621941G>A | CA389619834 | MGAT2 | c.673G>A (p.Ala225Thr) | dbSNP gnomAD v4 |
14 | g.49621941G>C | CA389619836 | MGAT2 | c.673G>C (p.Ala225Pro) | |
14 | g.49621941G= | CA2135804749 | MGAT2 | c.673G= (p.Ala225=) | |
14 | g.49621941G>T | CA389619837 | MGAT2 | c.673G>T (p.Ala225Ser) | |
14 | g.49621942C>A | CA389619839 | MGAT2 | c.674C>A (p.Ala225Asp) | |
14 | g.49621942C>G | CA389619841 | MGAT2 | c.674C>G (p.Ala225Gly) | |
14 | g.49621942C>T | CA389619843 | MGAT2 | c.674C>T (p.Ala225Val) | |
14 | g.49621943C>A | CA486349745 | MGAT2 | c.675C>A (p.Ala225=) | gnomAD v4 |
14 | g.49621943C>G | CA486349747 | MGAT2 | c.675C>G (p.Ala225=) | |
14 | g.49621943C>T | CA486349749 | MGAT2 | c.675C>T (p.Ala225=) | |
14 | g.49621944A>C | CA389619845 | MGAT2 | c.676A>C (p.Lys226Gln) | |
14 | g.49621944A>G | CA389619846 | MGAT2 | c.676A>G (p.Lys226Glu) | gnomAD v4 |
14 | g.49621944A>T | CA389619848 | MGAT2 | c.676A>T (p.Lys226Ter) | |
14 | g.49621945A= | CA2135804750 | MGAT2 | c.677A= (p.Lys226=) | |
14 | g.49621945A>C | CA389619852 | MGAT2 | c.677A>C (p.Lys226Thr) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.49621945A>G | CA389619855 | MGAT2 | c.677A>G (p.Lys226Arg) | dbSNP gnomAD v3 gnomAD v4 |
14 | g.49621945A>T | CA389619853 | MGAT2 | c.677A>T (p.Lys226Ile) | gnomAD v4 |
14 | g.49621946A>C | CA389619858 | MGAT2 | c.678A>C (p.Lys226Asn) | |
14 | g.49621946A>G | CA486349750 | MGAT2 | c.678A>G (p.Lys226=) | |
14 | g.49621946A>T | CA389619860 | MGAT2 | c.678A>T (p.Lys226Asn) | COSMIC |
14 | g.49621947T>A | CA389619862 | MGAT2 | c.679T>A (p.Phe227Ile) | |
14 | g.49621947T>C | CA389619867 | MGAT2 | c.679T>C (p.Phe227Leu) | |
14 | g.49621947T>G | CA389619864 | MGAT2 | c.679T>G (p.Phe227Val) | |
14 | g.49621948T>A | CA389619870 | MGAT2 | c.680T>A (p.Phe227Tyr) | |
14 | g.49621948T>C | CA389619875 | MGAT2 | c.680T>C (p.Phe227Ser) | |
14 | g.49621948T>G | CA389619873 | MGAT2 | c.680T>G (p.Phe227Cys) | |
14 | g.49621949C>A | CA389619877 | MGAT2 | c.681C>A (p.Phe227Leu) | |
14 | g.49621949C>G | CA389619879 | MGAT2 | c.681C>G (p.Phe227Leu) | |
14 | g.49621949C>T | CA486349754 | MGAT2 | c.681C>T (p.Phe227=) | |
14 | g.49621950T>A | CA389619882 | MGAT2 | c.682T>A (p.Ser228Thr) | |
14 | g.49621950T>C | CA389619885 | MGAT2 | c.682T>C (p.Ser228Pro) | |
14 | g.49621950T>G | CA389619887 | MGAT2 | c.682T>G (p.Ser228Ala) | |
14 | g.49621951C>A | CA389619890 | MGAT2 | c.683C>A (p.Ser228Tyr) | |
14 | g.49621951C= | CA2135804751 | MGAT2 | c.683C= (p.Ser228=) | |
14 | g.49621951C>G | CA389619892 | MGAT2 | c.683C>G (p.Ser228Cys) | |
14 | g.49621951C>T | CA260660759 | MGAT2 | c.683C>T (p.Ser228Phe) | dbSNP |
14 | g.49621952C>A | CA486349757 | MGAT2 | c.684C>A (p.Ser228=) | |
14 | g.49621952C= | CA2135804752 | MGAT2 | c.684C= (p.Ser228=) | |
14 | g.49621952C>G | CA486349758 | MGAT2 | c.684C>G (p.Ser228=) | |
14 | g.49621952C>T | CA486349761 | MGAT2 | c.684C>T (p.Ser228=) | dbSNP gnomAD v2 |
14 | g.49621952_49621956delinsCCAGA | CA2135804753 | MGAT2 | c.684_688delinsCCAGA (p.Ser228=) | |
14 | g.49621953C>A | CA389619894 | MGAT2 | c.685C>A (p.Gln229Lys) | |
14 | g.49621953C>G | CA389619897 | MGAT2 | c.685C>G (p.Gln229Glu) | |
14 | g.49621953C>T | CA389619898 | MGAT2 | c.685C>T (p.Gln229Ter) | |
14 | g.49621954_49621957del | CA2135804754 | MGAT2 | c.686_689del (p.Gln229ProfsTer16) | dbSNP |
14 | g.49621954A= | CA2135804755 | MGAT2 | c.686A= (p.Gln229=) | |
14 | g.49621954A>C | CA389619901 | MGAT2 | c.686A>C (p.Gln229Pro) | |
14 | g.49621954A>G | CA389619905 | MGAT2 | c.686A>G (p.Gln229Arg) | dbSNP gnomAD v2 gnomAD v4 |
14 | g.49621954A>T | CA389619903 | MGAT2 | c.686A>T (p.Gln229Leu) | |
14 | g.49621955G>A | CA486349762 | MGAT2 | c.687G>A (p.Gln229=) | |
14 | g.49621955G>C | CA389619907 | MGAT2 | c.687G>C (p.Gln229His) | gnomAD v4 |
14 | g.49621955G= | CA2135804756 | MGAT2 | c.687G= (p.Gln229=) | |
14 | g.49621955G>T | CA389619910 | MGAT2 | c.687G>T (p.Gln229His) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.49621956A= | CA2135804757 | MGAT2 | c.688A= (p.Thr230=) | |
14 | g.49621956A>C | CA389619912 | MGAT2 | c.688A>C (p.Thr230Pro) | ClinVar dbSNP gnomAD v4 |
14 | g.49621956A>G | CA389619914 | MGAT2 | c.688A>G (p.Thr230Ala) | |
14 | g.49621956A>T | CA389619917 | MGAT2 | c.688A>T (p.Thr230Ser) | |
14 | g.49621957C>A | CA389619920 | MGAT2 | c.689C>A (p.Thr230Asn) | |
14 | g.49621957C>G | CA389619922 | MGAT2 | c.689C>G (p.Thr230Ser) | |
14 | g.49621957C>T | CA389619924 | MGAT2 | c.689C>T (p.Thr230Ile) | |
14 | g.49621958C>A | CA486349770 | MGAT2 | c.690C>A (p.Thr230=) | |
14 | g.49621958C>G | CA486349771 | MGAT2 | c.690C>G (p.Thr230=) | |
14 | g.49621958C>T | CA486349769 | MGAT2 | c.690C>T (p.Thr230=) | |
14 | g.49621959A>C | CA389619929 | MGAT2 | c.691A>C (p.Lys231Gln) | |
14 | g.49621959A>G | CA389619931 | MGAT2 | c.691A>G (p.Lys231Glu) | |
14 | g.49621959A>T | CA389619927 | MGAT2 | c.691A>T (p.Lys231Ter) | |
14 | g.49621961dup | CA486349772 | MGAT2 | c.693dup (p.His232ThrfsTer?) | COSMIC |
14 | g.49621960A>C | CA389619934 | MGAT2 | c.692A>C (p.Lys231Thr) | |
14 | g.49621960A>G | CA389619936 | MGAT2 | c.692A>G (p.Lys231Arg) | |
14 | g.49621960A>T | CA389619939 | MGAT2 | c.692A>T (p.Lys231Ile) | |
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) | |
14 | g.49621976G>T | CA389620027 | MGAT2 | c.708G>T (p.Trp236Cys) | |
14 | g.49621977A= | CA2135804760 | MGAT2 | c.709A= (p.Lys237=) | |
14 | g.49621977A>C | CA389620038 | MGAT2 | c.709A>C (p.Lys237Gln) | |
14 | g.49621977A>G | CA389620040 | MGAT2 | c.709A>G (p.Lys237Glu) | gnomAD v4 |
14 | g.49621977A>T | CA389620043 | MGAT2 | c.709A>T (p.Lys237Ter) | dbSNP gnomAD v2 gnomAD v4 |
14 | g.49621978A>C | CA389620047 | MGAT2 | c.710A>C (p.Lys237Thr) | |
14 | g.49621978A>G | CA389620049 | MGAT2 | c.710A>G (p.Lys237Arg) | |
14 | g.49621978A>T | CA389620050 | MGAT2 | c.710A>T (p.Lys237Met) | |
14 | g.49621979G>A | CA486349797 | MGAT2 | c.711G>A (p.Lys237=) | dbSNP gnomAD v4 |
14 | g.49621979G>C | CA249931 | MGAT2 | c.711G>C (p.Lys237Asn) | ClinVar dbSNP |
14 | g.49621979G= | CA2135804761 | MGAT2 | c.711G= (p.Lys237=) | |
14 | g.49621979G>T | CA389620059 | MGAT2 | c.711G>T (p.Lys237Asn) | |
14 | g.49621980C>A | CA7172592 | MGAT2 | c.712C>A (p.Leu238Met) | dbSNP ExAC gnomAD v2 gnomAD v4 |
14 | g.49621980C= | CA2135804762 | MGAT2 | c.712C= (p.Leu238=) | |
14 | g.49621980C>G | CA389620062 | MGAT2 | c.712C>G (p.Leu238Val) | |
14 | g.49621980C>T | CA486349800 | MGAT2 | c.712C>T (p.Leu238=) | |
14 | g.49621981T>A | CA389620073 | MGAT2 | c.713T>A (p.Leu238Gln) | |
14 | g.49621981T>C | CA389620071 | MGAT2 | c.713T>C (p.Leu238Pro) | gnomAD v4 |
14 | g.49621981T>G | CA389620068 | MGAT2 | c.713T>G (p.Leu238Arg) | |
14 | g.49621982G>A | CA7172593 | MGAT2 | c.714G>A (p.Leu238=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.49621982G>C | CA486349804 | MGAT2 | c.714G>C (p.Leu238=) | |
14 | g.49621982G= | CA2135804763 | MGAT2 | c.714G= (p.Leu238=) | |
14 | g.49621982G>T | CA486349803 | MGAT2 | c.714G>T (p.Leu238=) | |
14 | g.49621983C>A | CA389620079 | MGAT2 | c.715C>A (p.His239Asn) | |
14 | g.49621983C= | CA2135804764 | MGAT2 | c.715C= (p.His239=) | |
14 | g.49621983C>G | CA389620088 | MGAT2 | c.715C>G (p.His239Asp) | |
14 | g.49621983C>T | CA389620090 | MGAT2 | c.715C>T (p.His239Tyr) | dbSNP |
14 | g.49621984A>C | CA389620093 | MGAT2 | c.716A>C (p.His239Pro) | |
14 | g.49621984A>G | CA389620094 | MGAT2 | c.716A>G (p.His239Arg) | |
14 | g.49621984A>T | CA389620096 | MGAT2 | c.716A>T (p.His239Leu) | |
14 | g.49621985T>A | CA389620097 | MGAT2 | c.717T>A (p.His239Gln) | |
14 | g.49621985T>C | CA486349807 | MGAT2 | c.717T>C (p.His239=) | |
14 | g.49621985T>G | CA389620099 | MGAT2 | c.717T>G (p.His239Gln) | |
14 | g.49621986T>A | CA389620102 | MGAT2 | c.718T>A (p.Phe240Ile) | |
14 | g.49621986T>C | CA389620105 | MGAT2 | c.718T>C (p.Phe240Leu) | |
14 | g.49621986T>G | CA389620108 | MGAT2 | c.718T>G (p.Phe240Val) | gnomAD v4 |
14 | g.49621987T>A | CA389620110 | MGAT2 | c.719T>A (p.Phe240Tyr) | |
14 | g.49621987T>C | CA389620116 | MGAT2 | c.719T>C (p.Phe240Ser) | |
14 | g.49621987T>G | CA389620109 | MGAT2 | c.719T>G (p.Phe240Cys) | |
14 | g.49621988T>A | CA389620119 | MGAT2 | c.720T>A (p.Phe240Leu) | |
14 | g.49621988T>C | CA486349811 | MGAT2 | c.720T>C (p.Phe240=) | |
14 | g.49621988T>G | CA389620124 | MGAT2 | c.720T>G (p.Phe240Leu) | |
14 | g.49621989G>A | CA389620126 | MGAT2 | c.721G>A (p.Val241Met) | |
14 | g.49621989G>C | CA389620127 | MGAT2 | c.721G>C (p.Val241Leu) | |
14 | g.49621989G= | CA2135804765 | MGAT2 | c.721G= (p.Val241=) | |
14 | g.49621989G>T | CA389620129 | MGAT2 | c.721G>T (p.Val241Leu) | dbSNP gnomAD v3 gnomAD v4 |
14 | g.49621990T>A | CA389620135 | MGAT2 | c.722T>A (p.Val241Glu) | |
14 | g.49621990T>C | CA260660767 | MGAT2 | c.722T>C (p.Val241Ala) | dbSNP |
14 | g.49621990T>G | CA389620133 | MGAT2 | c.722T>G (p.Val241Gly) | |
14 | g.49621990T= | CA2135804766 | MGAT2 | c.722T= (p.Val241=) | |
14 | g.49621991G>A | CA486349814 | MGAT2 | c.723G>A (p.Val241=) | dbSNP |
14 | g.49621991G>C | CA486349815 | MGAT2 | c.723G>C (p.Val241=) | |
14 | g.49621991G= | CA2135804767 | MGAT2 | c.723G= (p.Val241=) | |
14 | g.49621991G>T | CA486349816 | MGAT2 | c.723G>T (p.Val241=) | gnomAD v4 |
14 | g.49621992T>A | CA389620137 | MGAT2 | c.724T>A (p.Trp242Arg) | |
14 | g.49621992T>C | CA389620140 | MGAT2 | c.724T>C (p.Trp242Arg) | |
14 | g.49621992T>G | CA389620144 | MGAT2 | c.724T>G (p.Trp242Gly) | dbSNP |
14 | g.49621992T= | CA2135804768 | MGAT2 | c.724T= (p.Trp242=) | |
14 | g.49621993G>A | CA389620148 | MGAT2 | c.725G>A (p.Trp242Ter) | |
14 | g.49621993G>C | CA389620149 | MGAT2 | c.725G>C (p.Trp242Ser) | |
14 | g.49621993G>T | CA389620151 | MGAT2 | c.725G>T (p.Trp242Leu) | |
14 | g.49621994G>A | CA389620156 | MGAT2 | c.726G>A (p.Trp242Ter) | |
14 | g.49621994G>C | CA389620158 | MGAT2 | c.726G>C (p.Trp242Cys) | |
14 | g.49621994G>T | CA389620153 | MGAT2 | c.726G>T (p.Trp242Cys) | |
14 | g.49621995G>A | CA389620160 | MGAT2 | c.727G>A (p.Glu243Lys) | gnomAD v4 |
14 | g.49621995G>C | CA389620159 | MGAT2 | c.727G>C (p.Glu243Gln) | gnomAD v4 |
14 | g.49621995G>T | CA389620163 | MGAT2 | c.727G>T (p.Glu243Ter) | |
14 | g.49621996A>C | CA389620165 | MGAT2 | c.728A>C (p.Glu243Ala) | |
14 | g.49621996A>G | CA389620167 | MGAT2 | c.728A>G (p.Glu243Gly) | |
14 | g.49621996A>T | CA389620168 | MGAT2 | c.728A>T (p.Glu243Val) | |
14 | g.49621997A>C | CA389620170 | MGAT2 | c.729A>C (p.Glu243Asp) | |
14 | g.49621997A>G | CA486349824 | MGAT2 | c.729A>G (p.Glu243=) | |
14 | g.49621997A>T | CA389620171 | MGAT2 | c.729A>T (p.Glu243Asp) | |
14 | g.49621998A= | CA2135804769 | MGAT2 | c.730A= (p.Arg244=) | |
14 | g.49621998A>C | CA486349826 | MGAT2 | c.730A>C (p.Arg244=) | |
14 | g.49621998A>G | CA260660768 | MGAT2 | c.730A>G (p.Arg244Gly) | dbSNP gnomAD v4 |
14 | g.49621998A>T | CA389620175 | MGAT2 | c.730A>T (p.Arg244Ter) | |
14 | g.49621999G>A | CA389620179 | MGAT2 | c.731G>A (p.Arg244Lys) | gnomAD v4 |
14 | g.49621999G>C | CA389620180 | MGAT2 | c.731G>C (p.Arg244Thr) | |
14 | g.49621999G>T | CA389620182 | MGAT2 | c.731G>T (p.Arg244Ile) | |
14 | g.49622000A>C | CA389620184 | MGAT2 | c.732A>C (p.Arg244Ser) | gnomAD v4 |
14 | g.49622000A>G | CA486349830 | MGAT2 | c.732A>G (p.Arg244=) | |
14 | g.49622000A>T | CA389620186 | MGAT2 | c.732A>T (p.Arg244Ser) | |
14 | g.49622001G>A | CA7172594 | MGAT2 | c.733G>A (p.Val245Met) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
14 | g.49622001G>C | CA221941 | MGAT2 | c.733G>C (p.Val245Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.49622001G= | CA2135804770 | MGAT2 | c.733G= (p.Val245=) | |
14 | g.49622001G>T | CA389620190 | MGAT2 | c.733G>T (p.Val245Leu) | COSMIC |
14 | g.49622002T>A | CA389620194 | MGAT2 | c.734T>A (p.Val245Glu) | |
14 | g.49622002T>C | CA389620196 | MGAT2 | c.734T>C (p.Val245Ala) | |
14 | g.49622002T>G | CA389620198 | MGAT2 | c.734T>G (p.Val245Gly) | |
14 | g.49622003G>A | CA486349833 | MGAT2 | c.735G>A (p.Val245=) | dbSNP |
14 | g.49622003G>C | CA486349834 | MGAT2 | c.735G>C (p.Val245=) | |
14 | g.49622003G= | CA2135804771 | MGAT2 | c.735G= (p.Val245=) | |
14 | g.49622003G>T | CA486349835 | MGAT2 | c.735G>T (p.Val245=) | |
14 | g.49622004A>C | CA389620201 | MGAT2 | c.736A>C (p.Lys246Gln) | |
14 | g.49622004A>G | CA389620204 | MGAT2 | c.736A>G (p.Lys246Glu) | |
14 | g.49622004A>T | CA389620207 | MGAT2 | c.736A>T (p.Lys246Ter) | |
14 | g.49622007dup | CA2624726678 | MGAT2 | c.739dup (p.Ile247AsnfsTer?) | gnomAD v4 |
14 | g.49622005A>C | CA389620210 | MGAT2 | c.737A>C (p.Lys246Thr) | |
14 | g.49622005A>G | CA389620211 | MGAT2 | c.737A>G (p.Lys246Arg) | |
14 | g.49622005A>T | CA389620214 | MGAT2 | c.737A>T (p.Lys246Ile) | COSMIC |
14 | g.49622006A>C | CA389620219 | MGAT2 | c.738A>C (p.Lys246Asn) | |
14 | g.49622006A>G | CA486349840 | MGAT2 | c.738A>G (p.Lys246=) | |
14 | g.49622006A>T | CA389620221 | MGAT2 | c.738A>T (p.Lys246Asn) | |
14 | g.49622007A>C | CA389620234 | MGAT2 | c.739A>C (p.Ile247Leu) | |
14 | g.49622007A>G | CA389620237 | MGAT2 | c.739A>G (p.Ile247Val) | gnomAD v4 |
14 | g.49622007A>T | CA389620226 | MGAT2 | c.739A>T (p.Ile247Phe) | |
14 | g.49622008T>A | CA389620241 | MGAT2 | c.740T>A (p.Ile247Asn) | |
14 | g.49622008T>C | CA389620243 | MGAT2 | c.740T>C (p.Ile247Thr) | |
14 | g.49622008T>G | CA389620245 | MGAT2 | c.740T>G (p.Ile247Ser) | |
14 | g.49622009T>A | CA486349843 | MGAT2 | c.741T>A (p.Ile247=) | |
14 | g.49622009T>C | CA486349844 | MGAT2 | c.741T>C (p.Ile247=) | |
14 | g.49622009T>G | CA389620248 | MGAT2 | c.741T>G (p.Ile247Met) | |
14 | g.49622010C>A | CA389620251 | MGAT2 | c.742C>A (p.Leu248Ile) | gnomAD v4 |
14 | g.49622010C>G | CA389620252 | MGAT2 | c.742C>G (p.Leu248Val) | |
14 | g.49622010C>T | CA389620254 | MGAT2 | c.742C>T (p.Leu248Phe) | |
14 | g.49622011T>A | CA389620256 | MGAT2 | c.743T>A (p.Leu248His) | |
14 | g.49622011T>C | CA389620258 | MGAT2 | c.743T>C (p.Leu248Pro) | |
14 | g.49622011T>G | CA389620259 | MGAT2 | c.743T>G (p.Leu248Arg) | |
14 | g.49622012T>A | CA486349851 | MGAT2 | c.744T>A (p.Leu248=) | |
14 | g.49622012T>C | CA486349854 | MGAT2 | c.744T>C (p.Leu248=) | dbSNP gnomAD v2 gnomAD v4 |
14 | g.49622012T>G | CA486349856 | MGAT2 | c.744T>G (p.Leu248=) | |
14 | g.49622012T= | CA2135804772 | MGAT2 | c.744T= (p.Leu248=) | |
14 | g.49622013C>A | CA486349857 | MGAT2 | c.745C>A (p.Arg249=) | gnomAD v4 |
14 | g.49622013C= | CA2135804773 | MGAT2 | c.745C= (p.Arg249=) | |
14 | g.49622013C>G | CA389620262 | MGAT2 | c.745C>G (p.Arg249Gly) | |
14 | g.49622013C>T | CA389620264 | MGAT2 | c.745C>T (p.Arg249Ter) | ClinVar dbSNP |
14 | g.49622014G>A | CA389620267 | MGAT2 | c.746G>A (p.Arg249Gln) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.49622014G>C | CA389620268 | MGAT2 | c.746G>C (p.Arg249Pro) | |
14 | g.49622014G= | CA2135804774 | MGAT2 | c.746G= (p.Arg249=) | |
14 | g.49622014G>T | CA389620266 | MGAT2 | c.746G>T (p.Arg249Leu) | |
14 | g.49622015A>C | CA486349859 | MGAT2 | c.747A>C (p.Arg249=) | |
14 | g.49622015A>G | CA486349861 | MGAT2 | c.747A>G (p.Arg249=) | |
14 | g.49622015A>T | CA486349863 | MGAT2 | c.747A>T (p.Arg249=) | gnomAD v4 |
14 | g.49622016del | CA2624726679 | MGAT2 | c.748del (p.Asp250IlefsTer9) | gnomAD v4 |
14 | g.49622016G>A | CA389620274 | MGAT2 | c.748G>A (p.Asp250Asn) | gnomAD v4 |
14 | g.49622016G>C | CA389620275 | MGAT2 | c.748G>C (p.Asp250His) | |
14 | g.49622016G>T | CA389620276 | MGAT2 | c.748G>T (p.Asp250Tyr) | gnomAD v4 |
14 | g.49622017A>C | CA389620277 | MGAT2 | c.749A>C (p.Asp250Ala) | |
14 | g.49622017A>G | CA389620278 | MGAT2 | c.749A>G (p.Asp250Gly) | |
14 | g.49622017A>T | CA389620279 | MGAT2 | c.749A>T (p.Asp250Val) | |
14 | g.49622018T>A | CA389620281 | MGAT2 | c.750T>A (p.Asp250Glu) | |
14 | g.49622018T>C | CA486349864 | MGAT2 | c.750T>C (p.Asp250=) | |
14 | g.49622018T>G | CA389620283 | MGAT2 | c.750T>G (p.Asp250Glu) | |
14 | g.49622019T>A | CA7172595 | MGAT2 | c.751T>A (p.Tyr251Asn) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.49622019T>C | CA389620286 | MGAT2 | c.751T>C (p.Tyr251His) | |
14 | g.49622019T>G | CA389620287 | MGAT2 | c.751T>G (p.Tyr251Asp) | |
14 | g.49622019T= | CA2135804775 | MGAT2 | c.751T= (p.Tyr251=) | |
14 | g.49622020A= | CA2135804776 | MGAT2 | c.752A= (p.Tyr251=) | |
14 | g.49622020A>C | CA389620290 | MGAT2 | c.752A>C (p.Tyr251Ser) | gnomAD v4 |
14 | g.49622020A>G | CA389620291 | MGAT2 | c.752A>G (p.Tyr251Cys) | |
14 | g.49622020A>T | CA389620293 | MGAT2 | c.752A>T (p.Tyr251Phe) | |
14 | g.49622021T>A | CA389620297 | MGAT2 | c.753T>A (p.Tyr251Ter) | |
14 | g.49622021T>C | CA486349869 | MGAT2 | c.753T>C (p.Tyr251=) | gnomAD v4 |
14 | g.49622021T>G | CA389620295 | MGAT2 | c.753T>G (p.Tyr251Ter) | |
14 | g.49622021dup | CA913190931 | MGAT2 | c.753dup (p.Ala252CysfsTer?) | ClinVar dbSNP |
14 | g.49622022G>A | CA389620300 | MGAT2 | c.754G>A (p.Ala252Thr) | |
14 | g.49622022G>C | CA389620308 | MGAT2 | c.754G>C (p.Ala252Pro) | |
14 | g.49622022G>T | CA389620302 | MGAT2 | c.754G>T (p.Ala252Ser) | |
14 | g.49622023C>A | CA7172596 | MGAT2 | c.755C>A (p.Ala252Asp) | dbSNP ExAC gnomAD v3 gnomAD v4 |
14 | g.49622023C= | CA2135804777 | MGAT2 | c.755C= (p.Ala252=) | |
14 | g.49622023C>G | CA389620312 | MGAT2 | c.755C>G (p.Ala252Gly) | |
14 | g.49622023C>T | CA389620315 | MGAT2 | c.755C>T (p.Ala252Val) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.49622024T>A | CA486349875 | MGAT2 | c.756T>A (p.Ala252=) | |
14 | g.49622024T>C | CA486349877 | MGAT2 | c.756T>C (p.Ala252=) | |
14 | g.49622024T>G | CA486349876 | MGAT2 | c.756T>G (p.Ala252=) | |
14 | g.49622025G>A | CA389620319 | MGAT2 | c.757G>A (p.Gly253Ser) | |
14 | g.49622025G>C | CA389620321 | MGAT2 | c.757G>C (p.Gly253Arg) | |
14 | g.49622025G>T | CA389620323 | MGAT2 | c.757G>T (p.Gly253Cys) | |
14 | g.49622026G>A | CA389620327 | MGAT2 | c.758G>A (p.Gly253Asp) | |
14 | g.49622026G>C | CA389620328 | MGAT2 | c.758G>C (p.Gly253Ala) | gnomAD v4 |
14 | g.49622026G>T | CA389620329 | MGAT2 | c.758G>T (p.Gly253Val) | |
14 | g.49622027C>A | CA486349882 | MGAT2 | c.759C>A (p.Gly253=) | |
14 | g.49622027C>G | CA486349881 | MGAT2 | c.759C>G (p.Gly253=) | |
14 | g.49622027C>T | CA486349880 | MGAT2 | c.759C>T (p.Gly253=) | |
14 | g.49622028C>A | CA389620332 | MGAT2 | c.760C>A (p.Leu254Ile) | |
14 | g.49622028C= | CA2135804778 | MGAT2 | c.760C= (p.Leu254=) | |
14 | g.49622028C>G | CA389620335 | MGAT2 | c.760C>G (p.Leu254Val) | |
14 | g.49622028C>T | CA389620338 | MGAT2 | c.760C>T (p.Leu254Phe) | dbSNP gnomAD v3 gnomAD v4 |
14 | g.49622029T>A | CA389620343 | MGAT2 | c.761T>A (p.Leu254His) | |
14 | g.49622029T>C | CA389620342 | MGAT2 | c.761T>C (p.Leu254Pro) | |
14 | g.49622029T>G | CA389620340 | MGAT2 | c.761T>G (p.Leu254Arg) | |
14 | g.49622030T>A | CA486349886 | MGAT2 | c.762T>A (p.Leu254=) | |
14 | g.49622030T>C | CA486349890 | MGAT2 | c.762T>C (p.Leu254=) | |
14 | g.49622030T>G | CA486349888 | MGAT2 | c.762T>G (p.Leu254=) | |
14 | g.49622031A>C | CA389620346 | MGAT2 | c.763A>C (p.Ile255Leu) | |
14 | g.49622031A>G | CA389620348 | MGAT2 | c.763A>G (p.Ile255Val) | dbSNP |
14 | g.49622031A>T | CA389620349 | MGAT2 | c.763A>T (p.Ile255Leu) | gnomAD v4 |