| 14 | g.49621648_49621651del | CA2624726673 | MGAT2 | c.380_383del (p.Arg127ProfsTer?)
| gnomAD v4 |
| 14 | g.49621650C>A | CA389618174 | MGAT2 | c.382C>A (p.Pro128Thr)
| |
| 14 | g.49621650C>G | CA389618177 | MGAT2 | c.382C>G (p.Pro128Ala)
| gnomAD v4 |
| 14 | g.49621650C>T | CA389618181 | MGAT2 | c.382C>T (p.Pro128Ser)
| |
| 14 | g.49621651C>A | CA389618184 | MGAT2 | c.383C>A (p.Pro128His)
| |
| 14 | g.49621651C= | CA2135804450 | MGAT2 | c.383C= (p.Pro128=)
| |
| 14 | g.49621651C>G | CA389618186 | MGAT2 | c.383C>G (p.Pro128Arg)
| |
| 14 | g.49621651C>T | CA260660625 | MGAT2 | c.383C>T (p.Pro128Leu)
| dbSNP gnomAD v4 |
| 14 | g.49621652C>A | CA486350321 | MGAT2 | c.384C>A (p.Pro128=)
| |
| 14 | g.49621652C= | CA2135804453 | MGAT2 | c.384C= (p.Pro128=)
| |
| 14 | g.49621652C>G | CA7172533 | MGAT2 | c.384C>G (p.Pro128=)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.49621652C>T | CA486350322 | MGAT2 | c.384C>T (p.Pro128=)
| gnomAD v4 |
| 14 | g.49621653G>A | CA389618190 | MGAT2 | c.385G>A (p.Glu129Lys)
| dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.49621653G>C | CA389618193 | MGAT2 | c.385G>C (p.Glu129Gln)
| |
| 14 | g.49621653G= | CA2135804454 | MGAT2 | c.385G= (p.Glu129=)
| |
| 14 | g.49621653G>T | CA389618194 | MGAT2 | c.385G>T (p.Glu129Ter)
| |
| 14 | g.49621654A>C | CA389618195 | MGAT2 | c.386A>C (p.Glu129Ala)
| gnomAD v4 |
| 14 | g.49621654A>G | CA389618196 | MGAT2 | c.386A>G (p.Glu129Gly)
| gnomAD v4 |
| 14 | g.49621654A>T | CA389618197 | MGAT2 | c.386A>T (p.Glu129Val)
| |
| 14 | g.49621655A>C | CA389618199 | MGAT2 | c.387A>C (p.Glu129Asp)
| |
| 14 | g.49621655A>G | CA486350327 | MGAT2 | c.387A>G (p.Glu129=)
| |
| 14 | g.49621655A>T | CA389618200 | MGAT2 | c.387A>T (p.Glu129Asp)
| |
| 14 | g.49621656T>A | CA389618202 | MGAT2 | c.388T>A (p.Tyr130Asn)
| |
| 14 | g.49621656T>C | CA389618204 | MGAT2 | c.388T>C (p.Tyr130His)
| |
| 14 | g.49621656T>G | CA389618205 | MGAT2 | c.388T>G (p.Tyr130Asp)
| |
| 14 | g.49621657A>C | CA389618212 | MGAT2 | c.389A>C (p.Tyr130Ser)
| |
| 14 | g.49621657A>G | CA389618213 | MGAT2 | c.389A>G (p.Tyr130Cys)
| |
| 14 | g.49621657A>T | CA389618215 | MGAT2 | c.389A>T (p.Tyr130Phe)
| |
| 14 | g.49621658C>A | CA389618217 | MGAT2 | c.390C>A (p.Tyr130Ter)
| dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.49621658C= | CA2135804456 | MGAT2 | c.390C= (p.Tyr130=)
| |
| 14 | g.49621658C>G | CA389618219 | MGAT2 | c.390C>G (p.Tyr130Ter)
| |
| 14 | g.49621658C>T | CA486350337 | MGAT2 | c.390C>T (p.Tyr130=)
| |
| 14 | g.49621659C>A | CA389618816 | MGAT2 | c.391C>A (p.Leu131Ile)
| |
| 14 | g.49621659C>G | CA389618818 | MGAT2 | c.391C>G (p.Leu131Val)
| |
| 14 | g.49621659C>T | CA389618820 | MGAT2 | c.391C>T (p.Leu131Phe)
| |
| 14 | g.49621660T>A | CA389618822 | MGAT2 | c.392T>A (p.Leu131His)
| |
| 14 | g.49621660T>C | CA389618824 | MGAT2 | c.392T>C (p.Leu131Pro)
| |
| 14 | g.49621660T>G | CA389618826 | MGAT2 | c.392T>G (p.Leu131Arg)
| dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.49621660T= | CA2135804459 | MGAT2 | c.392T= (p.Leu131=)
| |
| 14 | g.49621661C>A | CA486349836 | MGAT2 | c.393C>A (p.Leu131=)
| |
| 14 | g.49621661C= | CA2135804461 | MGAT2 | c.393C= (p.Leu131=)
| |
| 14 | g.49621661C>G | CA7172534 | MGAT2 | c.393C>G (p.Leu131=)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.49621661C>T | CA7172535 | MGAT2 | c.393C>T (p.Leu131=)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.49621662A>C | CA486349838 | MGAT2 | c.394A>C (p.Arg132=)
| |
| 14 | g.49621662A>G | CA389618830 | MGAT2 | c.394A>G (p.Arg132Gly)
| gnomAD v4 |
| 14 | g.49621662A>T | CA389618832 | MGAT2 | c.394A>T (p.Arg132Ter)
| |
| 14 | g.49621663G>A | CA389618833 | MGAT2 | c.395G>A (p.Arg132Lys)
| |
| 14 | g.49621663G>C | CA389618836 | MGAT2 | c.395G>C (p.Arg132Thr)
| ClinVar COSMIC |
| 14 | g.49621663G>T | CA389618837 | MGAT2 | c.395G>T (p.Arg132Ile)
| |
| 14 | g.49621664A>C | CA389618839 | MGAT2 | c.396A>C (p.Arg132Ser)
| |
| 14 | g.49621664A>G | CA486349842 | MGAT2 | c.396A>G (p.Arg132=)
| |
| 14 | g.49621664A>T | CA389618841 | MGAT2 | c.396A>T (p.Arg132Ser)
| |
| 14 | g.49621665C>A | CA389618843 | MGAT2 | c.397C>A (p.Leu133Met)
| gnomAD v4 |
| 14 | g.49621665C= | CA2135804464 | MGAT2 | c.397C= (p.Leu133=)
| |
| 14 | g.49621665C>G | CA7172536 | MGAT2 | c.397C>G (p.Leu133Val)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.49621665C>T | CA260660629 | MGAT2 | c.397C>T (p.Leu133=)
| dbSNP |
| 14 | g.49621666T>A | CA389618846 | MGAT2 | c.398T>A (p.Leu133Gln)
| |
| 14 | g.49621666T>C | CA7172537 | MGAT2 | c.398T>C (p.Leu133Pro)
| dbSNP ExAC gnomAD v4 |
| 14 | g.49621666T>G | CA260660631 | MGAT2 | c.398T>G (p.Leu133Arg)
| dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.49621666T= | CA2135804468 | MGAT2 | c.398T= (p.Leu133=)
| |
| 14 | g.49621667G>A | CA486349850 | MGAT2 | c.399G>A (p.Leu133=)
| gnomAD v4 |
| 14 | g.49621667G>C | CA486349855 | MGAT2 | c.399G>C (p.Leu133=)
| |
| 14 | g.49621667G>T | CA486349852 | MGAT2 | c.399G>T (p.Leu133=)
| |
| 14 | g.49621668C>A | CA389618850 | MGAT2 | c.400C>A (p.Leu134Met)
| |
| 14 | g.49621668C= | CA2135804471 | MGAT2 | c.400C= (p.Leu134=)
| |
| 14 | g.49621668C>G | CA389618851 | MGAT2 | c.400C>G (p.Leu134Val)
| |
| 14 | g.49621668C>T | CA260660635 | MGAT2 | c.400C>T (p.Leu134=)
| dbSNP |
| 14 | g.49621669T>A | CA389618854 | MGAT2 | c.401T>A (p.Leu134Gln)
| |
| 14 | g.49621669T>C | CA389618856 | MGAT2 | c.401T>C (p.Leu134Pro)
| |
| 14 | g.49621669T>G | CA389618855 | MGAT2 | c.401T>G (p.Leu134Arg)
| |
| 14 | g.49621670G>A | CA486349860 | MGAT2 | c.402G>A (p.Leu134=)
| ClinVar dbSNP gnomAD v4 |
| 14 | g.49621670G>C | CA486349862 | MGAT2 | c.402G>C (p.Leu134=)
| |
| 14 | g.49621670G= | CA2135804476 | MGAT2 | c.402G= (p.Leu134=)
| |
| 14 | g.49621670G>T | CA7172538 | MGAT2 | c.402G>T (p.Leu134=)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.49621671C>A | CA389618858 | MGAT2 | c.403C>A (p.Leu135Met)
| gnomAD v4 |
| 14 | g.49621671C= | CA2135804479 | MGAT2 | c.403C= (p.Leu135=)
| |
| 14 | g.49621671C>G | CA389618860 | MGAT2 | c.403C>G (p.Leu135Val)
| dbSNP gnomAD v4 |
| 14 | g.49621671C>T | CA486349866 | MGAT2 | c.403C>T (p.Leu135=)
| gnomAD v4 |
| 14 | g.49621672T>A | CA389618862 | MGAT2 | c.404T>A (p.Leu135Gln)
| |
| 14 | g.49621672T>C | CA389618864 | MGAT2 | c.404T>C (p.Leu135Pro)
| dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.49621672T>G | CA389618866 | MGAT2 | c.404T>G (p.Leu135Arg)
| |
| 14 | g.49621672T= | CA2135804484 | MGAT2 | c.404T= (p.Leu135=)
| |
| 14 | g.49621672_49621674delinsTGG | CA2135804483 | MGAT2 | c.404_406delinsTGG (p.Leu135=)
| |
| 14 | g.49621673G>A | CA486349868 | MGAT2 | c.405G>A (p.Leu135=)
| gnomAD v4 |
| 14 | g.49621673G>C | CA486349870 | MGAT2 | c.405G>C (p.Leu135=)
| |
| 14 | g.49621673G>T | CA486349872 | MGAT2 | c.405G>T (p.Leu135=)
| |
| 14 | g.49621673_49621674del | CA7172539 | MGAT2 | c.405_406del (p.Asp136LeufsTer9)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.49621674G>A | CA7172540 | MGAT2 | c.406G>A (p.Asp136Asn)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.49621674G>C | CA389618868 | MGAT2 | c.406G>C (p.Asp136His)
| |
| 14 | g.49621674G= | CA2135804487 | MGAT2 | c.406G= (p.Asp136=)
| |
| 14 | g.49621674G>T | CA389618869 | MGAT2 | c.406G>T (p.Asp136Tyr)
| |
| 14 | g.49621675A= | CA2135804491 | MGAT2 | c.407A= (p.Asp136=)
| |
| 14 | g.49621675A>C | CA389618871 | MGAT2 | c.407A>C (p.Asp136Ala)
| |
| 14 | g.49621675A>G | CA389618873 | MGAT2 | c.407A>G (p.Asp136Gly)
| |
| 14 | g.49621675A>T | CA7172541 | MGAT2 | c.407A>T (p.Asp136Val)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.49621675_49621700delinsACTCACTTCGAAAAGCCCAGGGAATT | CA2135804490 | MGAT2 | c.407_432delinsACTCACTTCGAAAAGCCCAGGGAATT (p.Asp136=)
| |
| 14 | g.49621676C>A | CA389618879 | MGAT2 | c.408C>A (p.Asp136Glu)
| |
| 14 | g.49621676C>G | CA389618876 | MGAT2 | c.408C>G (p.Asp136Glu)
| |
| 14 | g.49621676C>T | CA486349878 | MGAT2 | c.408C>T (p.Asp136=)
| |
| 14 | g.49621676_49621700del | CA7172542 | MGAT2 | c.408_432del (p.Asp136GlufsTer20)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.49621677T>A | CA389618881 | MGAT2 | c.409T>A (p.Ser137Thr)
| |
| 14 | g.49621677T>C | CA389618883 | MGAT2 | c.409T>C (p.Ser137Pro)
| |
| 14 | g.49621677T>G | CA7172543 | MGAT2 | c.409T>G (p.Ser137Ala)
| dbSNP ExAC gnomAD v2 |
| 14 | g.49621677T= | CA2135804498 | MGAT2 | c.409T= (p.Ser137=)
| |
| 14 | g.49621678C>A | CA389618886 | MGAT2 | c.410C>A (p.Ser137Ter)
| |
| 14 | g.49621678C>G | CA389618887 | MGAT2 | c.410C>G (p.Ser137Ter)
| |
| 14 | g.49621678C>T | CA389618889 | MGAT2 | c.410C>T (p.Ser137Leu)
| |
| 14 | g.49621679A= | CA2135804501 | MGAT2 | c.411A= (p.Ser137=)
| |
| 14 | g.49621679A>C | CA486349884 | MGAT2 | c.411A>C (p.Ser137=)
| |
| 14 | g.49621679A>G | CA260660648 | MGAT2 | c.411A>G (p.Ser137=)
| dbSNP |
| 14 | g.49621679A>T | CA486349885 | MGAT2 | c.411A>T (p.Ser137=)
| ClinVar dbSNP |
| 14 | g.49621680C>A | CA389618891 | MGAT2 | c.412C>A (p.Leu138Ile)
| |
| 14 | g.49621680C>G | CA389618893 | MGAT2 | c.412C>G (p.Leu138Val)
| |
| 14 | g.49621680C>T | CA389618894 | MGAT2 | c.412C>T (p.Leu138Phe)
| |
| 14 | g.49621681T>A | CA389618897 | MGAT2 | c.413T>A (p.Leu138His)
| |
| 14 | g.49621681T>C | CA389618899 | MGAT2 | c.413T>C (p.Leu138Pro)
| |
| 14 | g.49621681T>G | CA389618900 | MGAT2 | c.413T>G (p.Leu138Arg)
| |
| 14 | g.49621682T>A | CA486349893 | MGAT2 | c.414T>A (p.Leu138=)
| |
| 14 | g.49621682T>C | CA486349892 | MGAT2 | c.414T>C (p.Leu138=)
| dbSNP gnomAD v4 |
| 14 | g.49621682T>G | CA486349894 | MGAT2 | c.414T>G (p.Leu138=)
| |
| 14 | g.49621682T= | CA2135804506 | MGAT2 | c.414T= (p.Leu138=)
| |
| 14 | g.49621683C>A | CA486349896 | MGAT2 | c.415C>A (p.Arg139=)
| gnomAD v4 |
| 14 | g.49621683C= | CA2135804509 | MGAT2 | c.415C= (p.Arg139=)
| |
| 14 | g.49621683C>G | CA389618902 | MGAT2 | c.415C>G (p.Arg139Gly)
| dbSNP gnomAD v4 |
| 14 | g.49621683C>T | CA389618904 | MGAT2 | c.415C>T (p.Arg139Ter)
| |
| 14 | g.49621684G>A | CA389618906 | MGAT2 | c.416G>A (p.Arg139Gln)
| |
| 14 | g.49621684G>C | CA389618909 | MGAT2 | c.416G>C (p.Arg139Pro)
| |
| 14 | g.49621684G= | CA2135804510 | MGAT2 | c.416G= (p.Arg139=)
| |
| 14 | g.49621684G>T | CA389618908 | MGAT2 | c.416G>T (p.Arg139Leu)
| dbSNP |
| 14 | g.49621685A>C | CA486349901 | MGAT2 | c.417A>C (p.Arg139=)
| |
| 14 | g.49621685A>G | CA486349902 | MGAT2 | c.417A>G (p.Arg139=)
| |
| 14 | g.49621685A>T | CA486349903 | MGAT2 | c.417A>T (p.Arg139=)
| |
| 14 | g.49621686A>C | CA389618911 | MGAT2 | c.418A>C (p.Lys140Gln)
| |
| 14 | g.49621686A>G | CA389618913 | MGAT2 | c.418A>G (p.Lys140Glu)
| |
| 14 | g.49621686A>T | CA389618912 | MGAT2 | c.418A>T (p.Lys140Ter)
| |
| 14 | g.49621687A= | CA2135804512 | MGAT2 | c.419A= (p.Lys140=)
| |
| 14 | g.49621687A>C | CA389618915 | MGAT2 | c.419A>C (p.Lys140Thr)
| |
| 14 | g.49621687A>G | CA7172544 | MGAT2 | c.419A>G (p.Lys140Arg)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.49621687A>T | CA389618917 | MGAT2 | c.419A>T (p.Lys140Ile)
| |
| 14 | g.49621688A= | CA2135804514 | MGAT2 | c.420A= (p.Lys140=)
| |
| 14 | g.49621688A>C | CA389618919 | MGAT2 | c.420A>C (p.Lys140Asn)
| |
| 14 | g.49621688A>G | CA486349908 | MGAT2 | c.420A>G (p.Lys140=)
| dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.49621688A>T | CA389618921 | MGAT2 | c.420A>T (p.Lys140Asn)
| |
| 14 | g.49621689G>A | CA389618923 | MGAT2 | c.421G>A (p.Ala141Thr)
| |
| 14 | g.49621689G>C | CA389618925 | MGAT2 | c.421G>C (p.Ala141Pro)
| |
| 14 | g.49621689G>T | CA389618927 | MGAT2 | c.421G>T (p.Ala141Ser)
| |
| 14 | g.49621690C>A | CA389618929 | MGAT2 | c.422C>A (p.Ala141Asp)
| |
| 14 | g.49621690C>G | CA389618931 | MGAT2 | c.422C>G (p.Ala141Gly)
| |
| 14 | g.49621690C>T | CA389618933 | MGAT2 | c.422C>T (p.Ala141Val)
| |
| 14 | g.49621691C>A | CA486349914 | MGAT2 | c.423C>A (p.Ala141=)
| |
| 14 | g.49621691C>G | CA486349915 | MGAT2 | c.423C>G (p.Ala141=)
| |
| 14 | g.49621691C>T | CA486349917 | MGAT2 | c.423C>T (p.Ala141=)
| |
| 14 | g.49621692C>A | CA389618937 | MGAT2 | c.424C>A (p.Gln142Lys)
| |
| 14 | g.49621692C= | CA2135804517 | MGAT2 | c.424C= (p.Gln142=)
| |
| 14 | g.49621692C>G | CA7172545 | MGAT2 | c.424C>G (p.Gln142Glu)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.49621692C>T | CA389618935 | MGAT2 | c.424C>T (p.Gln142Ter)
| |
| 14 | g.49621692_49621693delinsCA | CA2135804519 | MGAT2 | c.424_425delinsCA (p.Gln142=)
| |
| 14 | g.49621693del | CA614273686 | MGAT2 | c.425del (p.Gln142ArgfsTer22)
| dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.49621693A>C | CA389618940 | MGAT2 | c.425A>C (p.Gln142Pro)
| gnomAD v4 |
| 14 | g.49621693A>G | CA389618942 | MGAT2 | c.425A>G (p.Gln142Arg)
| |
| 14 | g.49621693A>T | CA389618943 | MGAT2 | c.425A>T (p.Gln142Leu)
| |
| 14 | g.49621694G>A | CA486349919 | MGAT2 | c.426G>A (p.Gln142=)
| dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.49621694G>C | CA389618945 | MGAT2 | c.426G>C (p.Gln142His)
| |
| 14 | g.49621694G= | CA2135804524 | MGAT2 | c.426G= (p.Gln142=)
| |
| 14 | g.49621694G>T | CA389618947 | MGAT2 | c.426G>T (p.Gln142His)
| |
| 14 | g.49621696del | CA2624726674 | MGAT2 | c.428del (p.Gly143GlufsTer21)
| gnomAD v4 |
| 14 | g.49621695G>A | CA389618949 | MGAT2 | c.427G>A (p.Gly143Arg)
| |
| 14 | g.49621695G>C | CA389618951 | MGAT2 | c.427G>C (p.Gly143Arg)
| |
| 14 | g.49621695G>T | CA389618952 | MGAT2 | c.427G>T (p.Gly143Ter)
| |
| 14 | g.49621696G>A | CA389618955 | MGAT2 | c.428G>A (p.Gly143Glu)
| gnomAD v4 |
| 14 | g.49621696G>C | CA389618956 | MGAT2 | c.428G>C (p.Gly143Ala)
| |
| 14 | g.49621696G= | CA2135804526 | MGAT2 | c.428G= (p.Gly143=)
| |
| 14 | g.49621696G>T | CA389618958 | MGAT2 | c.428G>T (p.Gly143Val)
| dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.49621697A= | CA2135804529 | MGAT2 | c.429A= (p.Gly143=)
| |
| 14 | g.49621697A>C | CA486349927 | MGAT2 | c.429A>C (p.Gly143=)
| |
| 14 | g.49621697A>G | CA486349929 | MGAT2 | c.429A>G (p.Gly143=)
| dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.49621697A>T | CA486349931 | MGAT2 | c.429A>T (p.Gly143=)
| |
| 14 | g.49621698A>C | CA389618963 | MGAT2 | c.430A>C (p.Ile144Leu)
| |
| 14 | g.49621698A>G | CA389618962 | MGAT2 | c.430A>G (p.Ile144Val)
| gnomAD v4 |
| 14 | g.49621698A>T | CA389618960 | MGAT2 | c.430A>T (p.Ile144Phe)
| |
| 14 | g.49621699T>A | CA389618965 | MGAT2 | c.431T>A (p.Ile144Asn)
| gnomAD v4 |
| 14 | g.49621699T>C | CA389618967 | MGAT2 | c.431T>C (p.Ile144Thr)
| |
| 14 | g.49621699T>G | CA389618969 | MGAT2 | c.431T>G (p.Ile144Ser)
| |
| 14 | g.49621700T>A | CA486349936 | MGAT2 | c.432T>A (p.Ile144=)
| |
| 14 | g.49621700T>C | CA486349935 | MGAT2 | c.432T>C (p.Ile144=)
| |
| 14 | g.49621700T>G | CA389618971 | MGAT2 | c.432T>G (p.Ile144Met)
| |
| 14 | g.49621701G>A | CA389618973 | MGAT2 | c.433G>A (p.Asp145Asn)
| gnomAD v4 |
| 14 | g.49621701G>C | CA389618975 | MGAT2 | c.433G>C (p.Asp145His)
| |
| 14 | g.49621701G>T | CA389618977 | MGAT2 | c.433G>T (p.Asp145Tyr)
| |
| 14 | g.49621702A>C | CA389618979 | MGAT2 | c.434A>C (p.Asp145Ala)
| |
| 14 | g.49621702A>G | CA389618981 | MGAT2 | c.434A>G (p.Asp145Gly)
| |
| 14 | g.49621702A>T | CA389618983 | MGAT2 | c.434A>T (p.Asp145Val)
| |
| 14 | g.49621703C>A | CA389618985 | MGAT2 | c.435C>A (p.Asp145Glu)
| |
| 14 | g.49621703C>G | CA389618987 | MGAT2 | c.435C>G (p.Asp145Glu)
| |
| 14 | g.49621703C>T | CA486349941 | MGAT2 | c.435C>T (p.Asp145=)
| gnomAD v4 |
| 14 | g.49621704A= | CA2135804533 | MGAT2 | c.436A= (p.Asn146=)
| |
| 14 | g.49621704A>C | CA389618991 | MGAT2 | c.436A>C (p.Asn146His)
| |
| 14 | g.49621704A>G | CA7172546 | MGAT2 | c.436A>G (p.Asn146Asp)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.49621704A>T | CA389618989 | MGAT2 | c.436A>T (p.Asn146Tyr)
| |
| 14 | g.49621705A= | CA2135804535 | MGAT2 | c.437A= (p.Asn146=)
| |
| 14 | g.49621705A>C | CA389618994 | MGAT2 | c.437A>C (p.Asn146Thr)
| dbSNP gnomAD v4 |
| 14 | g.49621705A>G | CA7172547 | MGAT2 | c.437A>G (p.Asn146Ser)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.49621705A>T | CA389618997 | MGAT2 | c.437A>T (p.Asn146Ile)
| |
| 14 | g.49621706C>A | CA389618999 | MGAT2 | c.438C>A (p.Asn146Lys)
| |
| 14 | g.49621706C= | CA2135804539 | MGAT2 | c.438C= (p.Asn146=)
| |
| 14 | g.49621706C>G | CA389619001 | MGAT2 | c.438C>G (p.Asn146Lys)
| |
| 14 | g.49621706C>T | CA7172548 | MGAT2 | c.438C>T (p.Asn146=)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.49621707G>A | CA389619003 | MGAT2 | c.439G>A (p.Val147Ile)
| dbSNP gnomAD v4 |
| 14 | g.49621707G>C | CA389619006 | MGAT2 | c.439G>C (p.Val147Leu)
| dbSNP gnomAD v4 |
| 14 | g.49621707G= | CA2135804544 | MGAT2 | c.439G= (p.Val147=)
| |
| 14 | g.49621707G>T | CA389619007 | MGAT2 | c.439G>T (p.Val147Phe)
| |
| 14 | g.49621708T>A | CA389619010 | MGAT2 | c.440T>A (p.Val147Asp)
| |
| 14 | g.49621708T>C | CA389619012 | MGAT2 | c.440T>C (p.Val147Ala)
| |
| 14 | g.49621708T>G | CA389619013 | MGAT2 | c.440T>G (p.Val147Gly)
| |
| 14 | g.49621709C>A | CA486349953 | MGAT2 | c.441C>A (p.Val147=)
| gnomAD v4 |
| 14 | g.49621709C>G | CA486349954 | MGAT2 | c.441C>G (p.Val147=)
| |
| 14 | g.49621709C>T | CA486349955 | MGAT2 | c.441C>T (p.Val147=)
| |
| 14 | g.49621710C>A | CA389619018 | MGAT2 | c.442C>A (p.Leu148Ile)
| gnomAD v4 |
| 14 | g.49621710C= | CA2135804546 | MGAT2 | c.442C= (p.Leu148=)
| |
| 14 | g.49621710C>G | CA389619016 | MGAT2 | c.442C>G (p.Leu148Val)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.49621710C>T | CA260660659 | MGAT2 | c.442C>T (p.Leu148Phe)
| dbSNP |
| 14 | g.49621711T>A | CA389619019 | MGAT2 | c.443T>A (p.Leu148His)
| |
| 14 | g.49621711T>C | CA389619023 | MGAT2 | c.443T>C (p.Leu148Pro)
| |
| 14 | g.49621711T>G | CA389619022 | MGAT2 | c.443T>G (p.Leu148Arg)
| |
| 14 | g.49621712C>A | CA486349958 | MGAT2 | c.444C>A (p.Leu148=)
| |
| 14 | g.49621712C>G | CA486349959 | MGAT2 | c.444C>G (p.Leu148=)
| gnomAD v4 |
| 14 | g.49621712C>T | CA486349960 | MGAT2 | c.444C>T (p.Leu148=)
| gnomAD v4 |
| 14 | g.49621713G>A | CA7172549 | MGAT2 | c.445G>A (p.Val149Ile)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.49621713G>C | CA389619026 | MGAT2 | c.445G>C (p.Val149Leu)
| |
| 14 | g.49621713G= | CA2135804550 | MGAT2 | c.445G= (p.Val149=)
| |
| 14 | g.49621713G>T | CA389619028 | MGAT2 | c.445G>T (p.Val149Phe)
| |
| 14 | g.49621714T>A | CA389619030 | MGAT2 | c.446T>A (p.Val149Asp)
| |
| 14 | g.49621714T>C | CA389619032 | MGAT2 | c.446T>C (p.Val149Ala)
| |
| 14 | g.49621714T>G | CA389619034 | MGAT2 | c.446T>G (p.Val149Gly)
| |
| 14 | g.49621715C>A | CA486349967 | MGAT2 | c.447C>A (p.Val149=)
| |
| 14 | g.49621715C>G | CA486349966 | MGAT2 | c.447C>G (p.Val149=)
| |
| 14 | g.49621715C>T | CA486349965 | MGAT2 | c.447C>T (p.Val149=)
| |
| 14 | g.49621716A>C | CA389619036 | MGAT2 | c.448A>C (p.Ile150Leu)
| |
| 14 | g.49621716A>G | CA389619038 | MGAT2 | c.448A>G (p.Ile150Val)
| gnomAD v4 |
| 14 | g.49621716A>T | CA389619039 | MGAT2 | c.448A>T (p.Ile150Phe)
| |
| 14 | g.49621717T>A | CA389619042 | MGAT2 | c.449T>A (p.Ile150Asn)
| |
| 14 | g.49621717T>C | CA389619044 | MGAT2 | c.449T>C (p.Ile150Thr)
| |
| 14 | g.49621717T>G | CA389619045 | MGAT2 | c.449T>G (p.Ile150Ser)
| |
| 14 | g.49621718C>A | CA486349971 | MGAT2 | c.450C>A (p.Ile150=)
| |
| 14 | g.49621718C>G | CA389619047 | MGAT2 | c.450C>G (p.Ile150Met)
| |
| 14 | g.49621718C>T | CA486349973 | MGAT2 | c.450C>T (p.Ile150=)
| |
| 14 | g.49621719T>A | CA389619049 | MGAT2 | c.451T>A (p.Phe151Ile)
| |
| 14 | g.49621719T>C | CA389619051 | MGAT2 | c.451T>C (p.Phe151Leu)
| |
| 14 | g.49621719T>G | CA389619053 | MGAT2 | c.451T>G (p.Phe151Val)
| gnomAD v4 |
| 14 | g.49621720T>A | CA389619056 | MGAT2 | c.452T>A (p.Phe151Tyr)
| |
| 14 | g.49621720T>C | CA389619058 | MGAT2 | c.452T>C (p.Phe151Ser)
| |
| 14 | g.49621720T>G | CA389619059 | MGAT2 | c.452T>G (p.Phe151Cys)
| |
| 14 | g.49621721T>A | CA389619061 | MGAT2 | c.453T>A (p.Phe151Leu)
| |
| 14 | g.49621721T>C | CA486349978 | MGAT2 | c.453T>C (p.Phe151=)
| gnomAD v4 |
| 14 | g.49621721T>G | CA389619063 | MGAT2 | c.453T>G (p.Phe151Leu)
| |
| 14 | g.49621722A>C | CA389619065 | MGAT2 | c.454A>C (p.Ser152Arg)
| |
| 14 | g.49621722A>G | CA389619066 | MGAT2 | c.454A>G (p.Ser152Gly)
| |
| 14 | g.49621722A>T | CA389619068 | MGAT2 | c.454A>T (p.Ser152Cys)
| |
| 14 | g.49621723G>A | CA389619071 | MGAT2 | c.455G>A (p.Ser152Asn)
| |
| 14 | g.49621723G>C | CA389619072 | MGAT2 | c.455G>C (p.Ser152Thr)
| |
| 14 | g.49621723G>T | CA389619074 | MGAT2 | c.455G>T (p.Ser152Ile)
| gnomAD v4 |
| 14 | g.49621724C>A | CA389619077 | MGAT2 | c.456C>A (p.Ser152Arg)
| |
| 14 | g.49621724C= | CA2135804553 | MGAT2 | c.456C= (p.Ser152=)
| |
| 14 | g.49621724C>G | CA389619079 | MGAT2 | c.456C>G (p.Ser152Arg)
| |
| 14 | g.49621724C>T | CA7172550 | MGAT2 | c.456C>T (p.Ser152=)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.49621725C>A | CA389619081 | MGAT2 | c.457C>A (p.His153Asn)
| |
| 14 | g.49621725C= | CA2135804557 | MGAT2 | c.457C= (p.His153=)
| |
| 14 | g.49621725C>G | CA389619082 | MGAT2 | c.457C>G (p.His153Asp)
| |
| 14 | g.49621725C>T | CA260660664 | MGAT2 | c.457C>T (p.His153Tyr)
| dbSNP |
| 14 | g.49621726A= | CA2135804560 | MGAT2 | c.458A= (p.His153=)
| |
| 14 | g.49621726A>C | CA389619085 | MGAT2 | c.458A>C (p.His153Pro)
| |
| 14 | g.49621726A>G | CA7172551 | MGAT2 | c.458A>G (p.His153Arg)
| dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 14 | g.49621726A>T | CA7172552 | MGAT2 | c.458A>T (p.His153Leu)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.49621727T>A | CA389619089 | MGAT2 | c.459T>A (p.His153Gln)
| |
| 14 | g.49621727T>C | CA486349991 | MGAT2 | c.459T>C (p.His153=)
| |
| 14 | g.49621727T>G | CA389619090 | MGAT2 | c.459T>G (p.His153Gln)
| |
| 14 | g.49621728G>A | CA389619092 | MGAT2 | c.460G>A (p.Asp154Asn)
| |
| 14 | g.49621728G>C | CA389619093 | MGAT2 | c.460G>C (p.Asp154His)
| |
| 14 | g.49621728G>T | CA389619094 | MGAT2 | c.460G>T (p.Asp154Tyr)
| |
| 14 | g.49621729A= | CA2135804565 | MGAT2 | c.461A= (p.Asp154=)
| |
| 14 | g.49621729A>C | CA389619096 | MGAT2 | c.461A>C (p.Asp154Ala)
| |
| 14 | g.49621729A>G | CA389619097 | MGAT2 | c.461A>G (p.Asp154Gly)
| dbSNP |
| 14 | g.49621729A>T | CA7172553 | MGAT2 | c.461A>T (p.Asp154Val)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.49621730C>A | CA389619100 | MGAT2 | c.462C>A (p.Asp154Glu)
| |
| 14 | g.49621730C= | CA2135804567 | MGAT2 | c.462C= (p.Asp154=)
| |
| 14 | g.49621730C>G | CA389619102 | MGAT2 | c.462C>G (p.Asp154Glu)
| dbSNP |
| 14 | g.49621730C>T | CA486349997 | MGAT2 | c.462C>T (p.Asp154=)
| |
| 14 | g.49621731T>A | CA7172554 | MGAT2 | c.463T>A (p.Phe155Ile)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.49621731T>C | CA260660671 | MGAT2 | c.463T>C (p.Phe155Leu)
| dbSNP |
| 14 | g.49621731T>G | CA389619106 | MGAT2 | c.463T>G (p.Phe155Val)
| |
| 14 | g.49621731T= | CA2135804569 | MGAT2 | c.463T= (p.Phe155=)
| |
| 14 | g.49621732T>A | CA389619108 | MGAT2 | c.464T>A (p.Phe155Tyr)
| |
| 14 | g.49621732T>C | CA389619110 | MGAT2 | c.464T>C (p.Phe155Ser)
| |
| 14 | g.49621732T>G | CA389619111 | MGAT2 | c.464T>G (p.Phe155Cys)
| |
| 14 | g.49621733C>A | CA389619113 | MGAT2 | c.465C>A (p.Phe155Leu)
| |
| 14 | g.49621733C>G | CA389619115 | MGAT2 | c.465C>G (p.Phe155Leu)
| gnomAD v4 COSMIC |
| 14 | g.49621733C>T | CA486350003 | MGAT2 | c.465C>T (p.Phe155=)
| |
| 14 | g.49621734T>A | CA389619117 | MGAT2 | c.466T>A (p.Trp156Arg)
| |
| 14 | g.49621734T>C | CA389619119 | MGAT2 | c.466T>C (p.Trp156Arg)
| gnomAD v4 |
| 14 | g.49621734T>G | CA389619121 | MGAT2 | c.466T>G (p.Trp156Gly)
| |
| 14 | g.49621735G>A | CA389619123 | MGAT2 | c.467G>A (p.Trp156Ter)
| |
| 14 | g.49621735G>C | CA389619126 | MGAT2 | c.467G>C (p.Trp156Ser)
| |
| 14 | g.49621735G= | CA2135804572 | MGAT2 | c.467G= (p.Trp156=)
| |
| 14 | g.49621735G>T | CA260660676 | MGAT2 | c.467G>T (p.Trp156Leu)
| dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.49621736G>A | CA389619127 | MGAT2 | c.468G>A (p.Trp156Ter)
| |
| 14 | g.49621736G>C | CA389619131 | MGAT2 | c.468G>C (p.Trp156Cys)
| |
| 14 | g.49621736G>T | CA389619129 | MGAT2 | c.468G>T (p.Trp156Cys)
| |
| 14 | g.49621737T>A | CA389619132 | MGAT2 | c.469T>A (p.Ser157Thr)
| |
| 14 | g.49621737T>C | CA389619134 | MGAT2 | c.469T>C (p.Ser157Pro)
| |
| 14 | g.49621737T>G | CA389619136 | MGAT2 | c.469T>G (p.Ser157Ala)
| |
| 14 | g.49621738C>A | CA389619138 | MGAT2 | c.470C>A (p.Ser157Ter)
| |
| 14 | g.49621738C= | CA2135804576 | MGAT2 | c.470C= (p.Ser157=)
| |
| 14 | g.49621738C>G | CA389619140 | MGAT2 | c.470C>G (p.Ser157Trp)
| |
| 14 | g.49621738C>T | CA389619141 | MGAT2 | c.470C>T (p.Ser157Leu)
| dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.49621739G>A | CA486350009 | MGAT2 | c.471G>A (p.Ser157=)
| |
| 14 | g.49621739G>C | CA486350010 | MGAT2 | c.471G>C (p.Ser157=)
| dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.49621739G= | CA2135804577 | MGAT2 | c.471G= (p.Ser157=)
| |
| 14 | g.49621739G>T | CA486350011 | MGAT2 | c.471G>T (p.Ser157=)
| gnomAD v4 |
| 14 | g.49621740A>C | CA389619143 | MGAT2 | c.472A>C (p.Thr158Pro)
| |
| 14 | g.49621740A>G | CA389619145 | MGAT2 | c.472A>G (p.Thr158Ala)
| |
| 14 | g.49621740A>T | CA389619146 | MGAT2 | c.472A>T (p.Thr158Ser)
| |
| 14 | g.49621741C>A | CA389619149 | MGAT2 | c.473C>A (p.Thr158Asn)
| |
| 14 | g.49621741C>G | CA389619150 | MGAT2 | c.473C>G (p.Thr158Ser)
| |
| 14 | g.49621741C>T | CA389619152 | MGAT2 | c.473C>T (p.Thr158Ile)
| gnomAD v4 |
| 14 | g.49621742C>A | CA486350014 | MGAT2 | c.474C>A (p.Thr158=)
| |
| 14 | g.49621742C= | CA2135804579 | MGAT2 | c.474C= (p.Thr158=)
| |
| 14 | g.49621742C>G | CA7172555 | MGAT2 | c.474C>G (p.Thr158=)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.49621742C>T | CA486350016 | MGAT2 | c.474C>T (p.Thr158=)
| |
| 14 | g.49621743G>A | CA389619159 | MGAT2 | c.475G>A (p.Glu159Lys)
| dbSNP |
| 14 | g.49621743G>C | CA389619157 | MGAT2 | c.475G>C (p.Glu159Gln)
| |
| 14 | g.49621743G= | CA2135804581 | MGAT2 | c.475G= (p.Glu159=)
| |
| 14 | g.49621743G>T | CA389619155 | MGAT2 | c.475G>T (p.Glu159Ter)
| |
| 14 | g.49621744A= | CA2135804585 | MGAT2 | c.476A= (p.Glu159=)
| |
| 14 | g.49621744A>C | CA389619161 | MGAT2 | c.476A>C (p.Glu159Ala)
| |
| 14 | g.49621744A>G | CA389619163 | MGAT2 | c.476A>G (p.Glu159Gly)
| dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.49621744A>T | CA389619165 | MGAT2 | c.476A>T (p.Glu159Val)
| |
| 14 | g.49621745G>A | CA7172556 | MGAT2 | c.477G>A (p.Glu159=)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.49621745G>C | CA389619167 | MGAT2 | c.477G>C (p.Glu159Asp)
| |
| 14 | g.49621745G= | CA2135804587 | MGAT2 | c.477G= (p.Glu159=)
| |
| 14 | g.49621745G>T | CA389619169 | MGAT2 | c.477G>T (p.Glu159Asp)
| |
| 14 | g.49621745_49621749delinsGATCA | CA2135804590 | MGAT2 | c.477_481delinsGATCA (p.Glu159=)
| |
| 14 | g.49621746A>C | CA389619171 | MGAT2 | c.478A>C (p.Ile160Leu)
| |
| 14 | g.49621746A>G | CA389619173 | MGAT2 | c.478A>G (p.Ile160Val)
| |
| 14 | g.49621746A>T | CA389619175 | MGAT2 | c.478A>T (p.Ile160Phe)
| |
| 14 | g.49621750_49621753del | CA2135804594 | MGAT2 | c.482_485del (p.Asn161SerfsTer2)
| dbSNP |
| 14 | g.49621747T>A | CA389619177 | MGAT2 | c.479T>A (p.Ile160Asn)
| |
| 14 | g.49621747T>C | CA389619179 | MGAT2 | c.479T>C (p.Ile160Thr)
| |
| 14 | g.49621747T>G | CA389619181 | MGAT2 | c.479T>G (p.Ile160Ser)
| gnomAD v4 |
| 14 | g.49621748C>A | CA486350021 | MGAT2 | c.480C>A (p.Ile160=)
| |
| 14 | g.49621748C>G | CA389619182 | MGAT2 | c.480C>G (p.Ile160Met)
| |
| 14 | g.49621748C>T | CA486350023 | MGAT2 | c.480C>T (p.Ile160=)
| |
| 14 | g.49621749A>C | CA389619188 | MGAT2 | c.481A>C (p.Asn161His)
| dbSNP |
| 14 | g.49621749A>G | CA389619186 | MGAT2 | c.481A>G (p.Asn161Asp)
| |
| 14 | g.49621749A>T | CA389619184 | MGAT2 | c.481A>T (p.Asn161Tyr)
| |
| 14 | g.49621750A= | CA2135804595 | MGAT2 | c.482A= (p.Asn161=)
| |
| 14 | g.49621750A>C | CA389619190 | MGAT2 | c.482A>C (p.Asn161Thr)
| |
| 14 | g.49621750A>G | CA389619192 | MGAT2 | c.482A>G (p.Asn161Ser)
| dbSNP gnomAD v4 |
| 14 | g.49621750A>T | CA389619194 | MGAT2 | c.482A>T (p.Asn161Ile)
| |
