| 14 | g.49621617G>A | CA260660616 | MGAT2 | c.349G>A (p.Glu117Lys)
| dbSNP gnomAD v4 |
| 14 | g.49621617G>C | CA7172530 | MGAT2 | c.349G>C (p.Glu117Gln)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.49621617G= | CA2135804415 | MGAT2 | c.349G= (p.Glu117=)
| |
| 14 | g.49621617G>T | CA389617994 | MGAT2 | c.349G>T (p.Glu117Ter)
| gnomAD v4 |
| 14 | g.49621618A= | CA2135804418 | MGAT2 | c.350A= (p.Glu117=)
| |
| 14 | g.49621618A>C | CA389617996 | MGAT2 | c.350A>C (p.Glu117Ala)
| gnomAD v4 |
| 14 | g.49621618A>G | CA389617997 | MGAT2 | c.350A>G (p.Glu117Gly)
| dbSNP |
| 14 | g.49621618A>T | CA389617999 | MGAT2 | c.350A>T (p.Glu117Val)
| |
| 14 | g.49621619G>A | CA486350200 | MGAT2 | c.351G>A (p.Glu117=)
| gnomAD v4 |
| 14 | g.49621619G>C | CA389618002 | MGAT2 | c.351G>C (p.Glu117Asp)
| |
| 14 | g.49621619G>T | CA389618004 | MGAT2 | c.351G>T (p.Glu117Asp)
| |
| 14 | g.49621626_49621631dup | CA706480375 | MGAT2 | c.358_363dup (p.Val121_Val122insLeuVal)
| dbSNP |
| 14 | g.49621620C>A | CA389618011 | MGAT2 | c.352C>A (p.Leu118Met)
| |
| 14 | g.49621620C>G | CA389618008 | MGAT2 | c.352C>G (p.Leu118Val)
| |
| 14 | g.49621620C>T | CA486350207 | MGAT2 | c.352C>T (p.Leu118=)
| |
| 14 | g.49621621T>A | CA389618014 | MGAT2 | c.353T>A (p.Leu118Gln)
| |
| 14 | g.49621621T>C | CA389618017 | MGAT2 | c.353T>C (p.Leu118Pro)
| |
| 14 | g.49621621T>G | CA389618019 | MGAT2 | c.353T>G (p.Leu118Arg)
| |
| 14 | g.49621622G>A | CA260660619 | MGAT2 | c.354G>A (p.Leu118=)
| ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.49621622G>C | CA486350213 | MGAT2 | c.354G>C (p.Leu118=)
| |
| 14 | g.49621622G= | CA2135804421 | MGAT2 | c.354G= (p.Leu118=)
| |
| 14 | g.49621622G>T | CA486350214 | MGAT2 | c.354G>T (p.Leu118=)
| |
| 14 | g.49621623G>A | CA389618022 | MGAT2 | c.355G>A (p.Val119Met)
| |
| 14 | g.49621623G>C | CA389618024 | MGAT2 | c.355G>C (p.Val119Leu)
| |
| 14 | g.49621623G>T | CA389618027 | MGAT2 | c.355G>T (p.Val119Leu)
| |
| 14 | g.49621624T>A | CA389618032 | MGAT2 | c.356T>A (p.Val119Glu)
| |
| 14 | g.49621624T>C | CA389618034 | MGAT2 | c.356T>C (p.Val119Ala)
| |
| 14 | g.49621624T>G | CA389618029 | MGAT2 | c.356T>G (p.Val119Gly)
| dbSNP |
| 14 | g.49621624T= | CA2135804426 | MGAT2 | c.356T= (p.Val119=)
| |
| 14 | g.49621625G>A | CA486350217 | MGAT2 | c.357G>A (p.Val119=)
| |
| 14 | g.49621625G>C | CA486350218 | MGAT2 | c.357G>C (p.Val119=)
| |
| 14 | g.49621625G>T | CA486350219 | MGAT2 | c.357G>T (p.Val119=)
| gnomAD v4 |
| 14 | g.49621626C>A | CA389618039 | MGAT2 | c.358C>A (p.Leu120Met)
| |
| 14 | g.49621626C= | CA2135804428 | MGAT2 | c.358C= (p.Leu120=)
| |
| 14 | g.49621626C>G | CA389618037 | MGAT2 | c.358C>G (p.Leu120Val)
| dbSNP |
| 14 | g.49621626C>T | CA486350225 | MGAT2 | c.358C>T (p.Leu120=)
| |
| 14 | g.49621627T>A | CA389618044 | MGAT2 | c.359T>A (p.Leu120Gln)
| |
| 14 | g.49621627T>C | CA389618042 | MGAT2 | c.359T>C (p.Leu120Pro)
| ClinVar |
| 14 | g.49621627T>G | CA389618047 | MGAT2 | c.359T>G (p.Leu120Arg)
| |
| 14 | g.49621628G>A | CA7172531 | MGAT2 | c.360G>A (p.Leu120=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.49621628G>C | CA486350232 | MGAT2 | c.360G>C (p.Leu120=)
| |
| 14 | g.49621628G= | CA2135804431 | MGAT2 | c.360G= (p.Leu120=)
| |
| 14 | g.49621628G>T | CA486350234 | MGAT2 | c.360G>T (p.Leu120=)
| |
| 14 | g.49621629G>A | CA389618054 | MGAT2 | c.361G>A (p.Val121Met)
| gnomAD v4 |
| 14 | g.49621629G>C | CA389618051 | MGAT2 | c.361G>C (p.Val121Leu)
| |
| 14 | g.49621629G>T | CA389618056 | MGAT2 | c.361G>T (p.Val121Leu)
| gnomAD v4 |
| 14 | g.49621630T>A | CA389618059 | MGAT2 | c.362T>A (p.Val121Glu)
| |
| 14 | g.49621630T>C | CA389618061 | MGAT2 | c.362T>C (p.Val121Ala)
| gnomAD v4 |
| 14 | g.49621630T>G | CA389618064 | MGAT2 | c.362T>G (p.Val121Gly)
| dbSNP |
| 14 | g.49621630T= | CA2135804434 | MGAT2 | c.362T= (p.Val121=)
| |
| 14 | g.49621631G>A | CA486350241 | MGAT2 | c.363G>A (p.Val121=)
| gnomAD v4 |
| 14 | g.49621631G>C | CA486350243 | MGAT2 | c.363G>C (p.Val121=)
| |
| 14 | g.49621631G= | CA2135804436 | MGAT2 | c.363G= (p.Val121=)
| |
| 14 | g.49621631G>T | CA486350248 | MGAT2 | c.363G>T (p.Val121=)
| dbSNP gnomAD v4 |
| 14 | g.49621632G>A | CA389618067 | MGAT2 | c.364G>A (p.Val122Ile)
| |
| 14 | g.49621632G>C | CA389618068 | MGAT2 | c.364G>C (p.Val122Leu)
| |
| 14 | g.49621632G>T | CA389618069 | MGAT2 | c.364G>T (p.Val122Phe)
| gnomAD v4 |
| 14 | g.49621633T>A | CA389618070 | MGAT2 | c.365T>A (p.Val122Asp)
| |
| 14 | g.49621633T>C | CA389618071 | MGAT2 | c.365T>C (p.Val122Ala)
| |
| 14 | g.49621633T>G | CA389618072 | MGAT2 | c.365T>G (p.Val122Gly)
| dbSNP |
| 14 | g.49621633T= | CA2135804438 | MGAT2 | c.365T= (p.Val122=)
| |
| 14 | g.49621634C>A | CA486350258 | MGAT2 | c.366C>A (p.Val122=)
| gnomAD v4 |
| 14 | g.49621634C>G | CA486350256 | MGAT2 | c.366C>G (p.Val122=)
| |
| 14 | g.49621634C>T | CA486350255 | MGAT2 | c.366C>T (p.Val122=)
| |
| 14 | g.49621635C>A | CA389618073 | MGAT2 | c.367C>A (p.Gln123Lys)
| gnomAD v4 |
| 14 | g.49621635C>G | CA389618074 | MGAT2 | c.367C>G (p.Gln123Glu)
| |
| 14 | g.49621635C>T | CA389618076 | MGAT2 | c.367C>T (p.Gln123Ter)
| |
| 14 | g.49621636A= | CA2135804440 | MGAT2 | c.368A= (p.Gln123=)
| |
| 14 | g.49621636A>C | CA389618082 | MGAT2 | c.368A>C (p.Gln123Pro)
| |
| 14 | g.49621636A>G | CA389618077 | MGAT2 | c.368A>G (p.Gln123Arg)
| dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.49621636A>T | CA389618079 | MGAT2 | c.368A>T (p.Gln123Leu)
| |
| 14 | g.49621637G>A | CA486350272 | MGAT2 | c.369G>A (p.Gln123=)
| dbSNP gnomAD v4 |
| 14 | g.49621637G>C | CA389618083 | MGAT2 | c.369G>C (p.Gln123His)
| |
| 14 | g.49621637G= | CA2135804443 | MGAT2 | c.369G= (p.Gln123=)
| |
| 14 | g.49621637G>T | CA389618085 | MGAT2 | c.369G>T (p.Gln123His)
| |
| 14 | g.49621638G>A | CA389618088 | MGAT2 | c.370G>A (p.Val124Met)
| |
| 14 | g.49621638G>C | CA389618089 | MGAT2 | c.370G>C (p.Val124Leu)
| |
| 14 | g.49621638G>T | CA389618091 | MGAT2 | c.370G>T (p.Val124Leu)
| gnomAD v4 |
| 14 | g.49621639T>A | CA389618093 | MGAT2 | c.371T>A (p.Val124Glu)
| |
| 14 | g.49621639T>C | CA389618096 | MGAT2 | c.371T>C (p.Val124Ala)
| |
| 14 | g.49621639T>G | CA389618098 | MGAT2 | c.371T>G (p.Val124Gly)
| dbSNP |
| 14 | g.49621639T= | CA2135804444 | MGAT2 | c.371T= (p.Val124=)
| |
| 14 | g.49621640G>A | CA486350282 | MGAT2 | c.372G>A (p.Val124=)
| |
| 14 | g.49621640G>C | CA486350284 | MGAT2 | c.372G>C (p.Val124=)
| |
| 14 | g.49621640G>T | CA486350283 | MGAT2 | c.372G>T (p.Val124=)
| |
| 14 | g.49621641C>A | CA389618100 | MGAT2 | c.373C>A (p.His125Asn)
| |
| 14 | g.49621641C>G | CA389618102 | MGAT2 | c.373C>G (p.His125Asp)
| |
| 14 | g.49621641C>T | CA389618105 | MGAT2 | c.373C>T (p.His125Tyr)
| |
| 14 | g.49621642A>C | CA389618110 | MGAT2 | c.374A>C (p.His125Pro)
| gnomAD v4 |
| 14 | g.49621642A>G | CA389618113 | MGAT2 | c.374A>G (p.His125Arg)
| |
| 14 | g.49621642A>T | CA389618108 | MGAT2 | c.374A>T (p.His125Leu)
| |
| 14 | g.49621643T>A | CA389618122 | MGAT2 | c.375T>A (p.His125Gln)
| |
| 14 | g.49621643T>C | CA486350293 | MGAT2 | c.375T>C (p.His125=)
| |
| 14 | g.49621643T>G | CA389618124 | MGAT2 | c.375T>G (p.His125Gln)
| |
| 14 | g.49621644A>C | CA389618126 | MGAT2 | c.376A>C (p.Asn126His)
| |
| 14 | g.49621644A>G | CA389618128 | MGAT2 | c.376A>G (p.Asn126Asp)
| |
| 14 | g.49621644A>T | CA389618132 | MGAT2 | c.376A>T (p.Asn126Tyr)
| |
| 14 | g.49621645A>C | CA389618133 | MGAT2 | c.377A>C (p.Asn126Thr)
| |
| 14 | g.49621645A>G | CA389618136 | MGAT2 | c.377A>G (p.Asn126Ser)
| gnomAD v4 |
| 14 | g.49621645A>T | CA389618139 | MGAT2 | c.377A>T (p.Asn126Ile)
| |
| 14 | g.49621646C>A | CA389618141 | MGAT2 | c.378C>A (p.Asn126Lys)
| |
| 14 | g.49621646C= | CA2135804446 | MGAT2 | c.378C= (p.Asn126=)
| |
| 14 | g.49621646C>G | CA389618143 | MGAT2 | c.378C>G (p.Asn126Lys)
| |
| 14 | g.49621646C>T | CA7172532 | MGAT2 | c.378C>T (p.Asn126=)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.49621648_49621651del | CA2624726673 | MGAT2 | c.380_383del (p.Arg127ProfsTer?)
| gnomAD v4 |
| 14 | g.49621647C>A | CA486350305 | MGAT2 | c.379C>A (p.Arg127=)
| |
| 14 | g.49621647C= | CA2135804448 | MGAT2 | c.379C= (p.Arg127=)
| |
| 14 | g.49621647C>G | CA389618152 | MGAT2 | c.379C>G (p.Arg127Gly)
| dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.49621647C>T | CA389618154 | MGAT2 | c.379C>T (p.Arg127Trp)
| |
| 14 | g.49621648G>A | CA389618170 | MGAT2 | c.380G>A (p.Arg127Gln)
| |
| 14 | g.49621648G>C | CA389618160 | MGAT2 | c.380G>C (p.Arg127Pro)
| |
| 14 | g.49621648G>T | CA389618157 | MGAT2 | c.380G>T (p.Arg127Leu)
| |
| 14 | g.49621649G>A | CA486350310 | MGAT2 | c.381G>A (p.Arg127=)
| gnomAD v4 |
| 14 | g.49621649G>C | CA486350312 | MGAT2 | c.381G>C (p.Arg127=)
| gnomAD v4 |
| 14 | g.49621649G>T | CA486350314 | MGAT2 | c.381G>T (p.Arg127=)
| |
| 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)
| |
