Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.152868937A>CCA415287350NSDHLc.943A>C (p.Ser315Arg)
c.991A>C (p.Ser331Arg)
Xg.152868937A>GCA415287351NSDHLc.943A>G (p.Ser315Gly)
c.991A>G (p.Ser331Gly)
Xg.152868937A>TCA415287352NSDHLc.943A>T (p.Ser315Cys)
c.991A>T (p.Ser331Cys)
Xg.152868938G>ACA415287355NSDHLc.944G>A (p.Ser315Asn)
c.992G>A (p.Ser331Asn)
Xg.152868938G>CCA415287354NSDHLc.944G>C (p.Ser315Thr)
c.992G>C (p.Ser331Thr)
Xg.152868938G>TCA415287353NSDHLc.944G>T (p.Ser315Ile)
c.992G>T (p.Ser331Ile)
Xg.152868939T>ACA415287356NSDHLc.945T>A (p.Ser315Arg)
c.993T>A (p.Ser331Arg)
 COSMIC
Xg.152868939T>CCA519182679NSDHLc.945T>C (p.Ser315=)
c.993T>C (p.Ser331=)
 gnomAD v4
Xg.152868939T>GCA415287357NSDHLc.945T>G (p.Ser315Arg)
c.993T>G (p.Ser331Arg)
Xg.152868940C>ACA415287358NSDHLc.946C>A (p.Pro316Thr)
c.994C>A (p.Pro332Thr)
Xg.152868940C=CA2466154419NSDHLc.946C= (p.Pro316=)
c.994C= (p.Pro332=)
Xg.152868940C>GCA415287359NSDHLc.946C>G (p.Pro316Ala)
c.994C>G (p.Pro332Ala)
 dbSNP gnomAD v2 gnomAD v4
Xg.152868940C>TCA415287360NSDHLc.946C>T (p.Pro316Ser)
c.994C>T (p.Pro332Ser)
 gnomAD v4
Xg.152868941C>ACA415287361NSDHLc.947C>A (p.Pro316His)
c.995C>A (p.Pro332His)
Xg.152868941C=CA2466154420NSDHLc.947C= (p.Pro316=)
c.995C= (p.Pro332=)
Xg.152868941C>GCA10544883NSDHLc.947C>G (p.Pro316Arg)
c.995C>G (p.Pro332Arg)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
Xg.152868941C>TCA415287362NSDHLc.947C>T (p.Pro316Leu)
c.995C>T (p.Pro332Leu)
 gnomAD v4
Xg.152868942T>ACA519182686NSDHLc.948T>A (p.Pro316=)
c.996T>A (p.Pro332=)
Xg.152868942T>CCA519182687NSDHLc.948T>C (p.Pro316=)
c.996T>C (p.Pro332=)
Xg.152868942T>GCA519182688NSDHLc.948T>G (p.Pro316=)
c.996T>G (p.Pro332=)
Xg.152868943G>ACA415287363NSDHLc.949G>A (p.Val317Ile)
c.997G>A (p.Val333Ile)
Xg.152868943G>CCA415287364NSDHLc.949G>C (p.Val317Leu)
c.997G>C (p.Val333Leu)
Xg.152868943G>TCA415287365NSDHLc.949G>T (p.Val317Phe)
c.997G>T (p.Val333Phe)
Xg.152868944T>ACA415287368NSDHLc.950T>A (p.Val317Asp)
c.998T>A (p.Val333Asp)
 dbSNP
Xg.152868944T>CCA415287367NSDHLc.950T>C (p.Val317Ala)
c.998T>C (p.Val333Ala)
Xg.152868944T>GCA415287366NSDHLc.950T>G (p.Val317Gly)
c.998T>G (p.Val333Gly)
Xg.152868944T=CA2466154421NSDHLc.950T= (p.Val317=)
c.998T= (p.Val333=)
Xg.152868945C>ACA519182693NSDHLc.951C>A (p.Val317=)
c.999C>A (p.Val333=)
Xg.152868945C>GCA519182694NSDHLc.951C>G (p.Val317=)
c.999C>G (p.Val333=)
Xg.152868945C>TCA519182697NSDHLc.951C>T (p.Val317=)
c.999C>T (p.Val333=)
Xg.152868946A>CCA415287369NSDHLc.952A>C (p.Ile318Leu)
c.1000A>C (p.Ile334Leu)
Xg.152868946A>GCA415287370NSDHLc.952A>G (p.Ile318Val)
c.1000A>G (p.Ile334Val)
Xg.152868946A>TCA415287371NSDHLc.952A>T (p.Ile318Phe)
c.1000A>T (p.Ile334Phe)
Xg.152868947T>ACA415287372NSDHLc.953T>A (p.Ile318Asn)
c.1001T>A (p.Ile334Asn)
 gnomAD v4
Xg.152868947T>CCA415287373NSDHLc.953T>C (p.Ile318Thr)
c.1001T>C (p.Ile334Thr)
 COSMIC
Xg.152868947T>GCA415287374NSDHLc.953T>G (p.Ile318Ser)
c.1001T>G (p.Ile334Ser)
Xg.152868948C>ACA519182702NSDHLc.954C>A (p.Ile318=)
c.1002C>A (p.Ile334=)
Xg.152868948C=CA2466154422NSDHLc.954C= (p.Ile318=)
c.1002C= (p.Ile334=)
Xg.152868948C>GCA415287375NSDHLc.954C>G (p.Ile318Met)
c.1002C>G (p.Ile334Met)
 dbSNP gnomAD v2 gnomAD v4
Xg.152868948C>TCA519182708NSDHLc.954C>T (p.Ile318=)
c.1002C>T (p.Ile334=)
 dbSNP
Xg.152868949C>ACA415287376NSDHLc.955C>A (p.Gln319Lys)
c.1003C>A (p.Gln335Lys)
Xg.152868949C=CA2466154423NSDHLc.955C= (p.Gln319=)
c.1003C= (p.Gln335=)
Xg.152868949C>GCA10544884NSDHLc.955C>G (p.Gln319Glu)
c.1003C>G (p.Gln335Glu)
 dbSNP ExAC gnomAD v2 gnomAD v4
Xg.152868949C>TCA415287377NSDHLc.955C>T (p.Gln319Ter)
c.1003C>T (p.Gln335Ter)
Xg.152868950A>CCA415287378NSDHLc.956A>C (p.Gln319Pro)
c.1004A>C (p.Gln335Pro)
Xg.152868950A>GCA415287379NSDHLc.956A>G (p.Gln319Arg)
c.1004A>G (p.Gln335Arg)
Xg.152868950A>TCA415287380NSDHLc.956A>T (p.Gln319Leu)
c.1004A>T (p.Gln335Leu)
Xg.152868951G>ACA519182710NSDHLc.957G>A (p.Gln319=)
c.1005G>A (p.Gln335=)
Xg.152868951G>CCA415287382NSDHLc.957G>C (p.Gln319His)
c.1005G>C (p.Gln335His)
 gnomAD v4
Xg.152868951G>TCA415287381NSDHLc.957G>T (p.Gln319His)
c.1005G>T (p.Gln335His)
 gnomAD v4
Xg.152868952C>ACA415287383NSDHLc.958C>A (p.Leu320Met)
c.1006C>A (p.Leu336Met)
Xg.152868952C=CA2466154424NSDHLc.958C= (p.Leu320=)
c.1006C= (p.Leu336=)
Xg.152868952C>GCA415287384NSDHLc.958C>G (p.Leu320Val)
c.1006C>G (p.Leu336Val)
Xg.152868952C>TCA519182711NSDHLc.958C>T (p.Leu320=)
c.1006C>T (p.Leu336=)
 dbSNP gnomAD v2 gnomAD v4
Xg.152868953T>ACA415287385NSDHLc.959T>A (p.Leu320Gln)
c.1007T>A (p.Leu336Gln)
Xg.152868953T>CCA415287386NSDHLc.959T>C (p.Leu320Pro)
c.1007T>C (p.Leu336Pro)
Xg.152868953T>GCA415287387NSDHLc.959T>G (p.Leu320Arg)
c.1007T>G (p.Leu336Arg)
Xg.152868954G>ACA519182715NSDHLc.960G>A (p.Leu320=)
c.1008G>A (p.Leu336=)
Xg.152868954G>CCA519182716NSDHLc.960G>C (p.Leu320=)
c.1008G>C (p.Leu336=)
Xg.152868954G=CA2466154425NSDHLc.960G= (p.Leu320=)
c.1008G= (p.Leu336=)
Xg.152868954G>TCA519182717NSDHLc.960G>T (p.Leu320=)
c.1008G>T (p.Leu336=)
 dbSNP gnomAD v2
Xg.152868955C>ACA415287388NSDHLc.961C>A (p.Gln321Lys)
c.1009C>A (p.Gln337Lys)
Xg.152868955C>GCA415287389NSDHLc.961C>G (p.Gln321Glu)
c.1009C>G (p.Gln337Glu)
Xg.152868955C>TCA415287390NSDHLc.961C>T (p.Gln321Ter)
c.1009C>T (p.Gln337Ter)
Xg.152868956A>CCA415287391NSDHLc.962A>C (p.Gln321Pro)
c.1010A>C (p.Gln337Pro)
Xg.152868956A>GCA415287392NSDHLc.962A>G (p.Gln321Arg)
c.1010A>G (p.Gln337Arg)
 gnomAD v4
Xg.152868956A>TCA415287393NSDHLc.962A>T (p.Gln321Leu)
c.1010A>T (p.Gln337Leu)
Xg.152868957G>ACA519182721NSDHLc.963G>A (p.Gln321=)
c.1011G>A (p.Gln337=)
Xg.152868957G>CCA415287394NSDHLc.963G>C (p.Gln321His)
c.1011G>C (p.Gln337His)
 ClinVar dbSNP gnomAD v3 gnomAD v4
Xg.152868957G=CA2466154426NSDHLc.963G= (p.Gln321=)
c.1011G= (p.Gln337=)
Xg.152868957G>TCA415287395NSDHLc.963G>T (p.Gln321His)
c.1011G>T (p.Gln337His)
Xg.152868958C>ACA415287398NSDHLc.964C>A (p.Pro322Thr)
c.1012C>A (p.Pro338Thr)
Xg.152868958C>GCA415287396NSDHLc.964C>G (p.Pro322Ala)
c.1012C>G (p.Pro338Ala)
 ClinVar
Xg.152868958C>TCA415287397NSDHLc.964C>T (p.Pro322Ser)
c.1012C>T (p.Pro338Ser)
 gnomAD v4
Xg.152868959C>ACA415287399NSDHLc.965C>A (p.Pro322His)
c.1013C>A (p.Pro338His)
Xg.152868959C=CA2466154427NSDHLc.965C= (p.Pro322=)
c.1013C= (p.Pro338=)
Xg.152868959C>GCA337613783NSDHLc.965C>G (p.Pro322Arg)
c.1013C>G (p.Pro338Arg)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.152868959C>TCA415287400NSDHLc.965C>T (p.Pro322Leu)
c.1013C>T (p.Pro338Leu)
Xg.152868960C>ACA519182725NSDHLc.966C>A (p.Pro322=)
c.1014C>A (p.Pro338=)
Xg.152868960C=CA2466154428NSDHLc.966C= (p.Pro322=)
c.1014C= (p.Pro338=)
Xg.152868960C>GCA519182726NSDHLc.966C>G (p.Pro322=)
c.1014C>G (p.Pro338=)
Xg.152868960C>TCA10544885NSDHLc.966C>T (p.Pro322=)
c.1014C>T (p.Pro338=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.152868961A>CCA415287401NSDHLc.967A>C (p.Thr323Pro)
c.1015A>C (p.Thr339Pro)
Xg.152868961A>GCA415287402NSDHLc.967A>G (p.Thr323Ala)
c.1015A>G (p.Thr339Ala)
Xg.152868961A>TCA415287403NSDHLc.967A>T (p.Thr323Ser)
c.1015A>T (p.Thr339Ser)
Xg.152868962C>ACA415287404NSDHLc.968C>A (p.Thr323Asn)
c.1016C>A (p.Thr339Asn)
Xg.152868962C>GCA415287405NSDHLc.968C>G (p.Thr323Ser)
c.1016C>G (p.Thr339Ser)
Xg.152868962C>TCA415287406NSDHLc.968C>T (p.Thr323Ile)
c.1016C>T (p.Thr339Ile)
Xg.152868963C>ACA519182731NSDHLc.969C>A (p.Thr323=)
c.1017C>A (p.Thr339=)
Xg.152868963C=CA2466154429NSDHLc.969C= (p.Thr323=)
c.1017C= (p.Thr339=)
Xg.152868963C>GCA519182732NSDHLc.969C>G (p.Thr323=)
c.1017C>G (p.Thr339=)
Xg.152868963C>TCA519182733NSDHLc.969C>T (p.Thr323=)
c.1017C>T (p.Thr339=)
 dbSNP
Xg.152868964T>ACA415287407NSDHLc.970T>A (p.Phe324Ile)
c.1018T>A (p.Phe340Ile)
Xg.152868964T>CCA415287408NSDHLc.970T>C (p.Phe324Leu)
c.1018T>C (p.Phe340Leu)
Xg.152868964T>GCA415287409NSDHLc.970T>G (p.Phe324Val)
c.1018T>G (p.Phe340Val)
Xg.152868965T>ACA415287412NSDHLc.971T>A (p.Phe324Tyr)
c.1019T>A (p.Phe340Tyr)
Xg.152868965T>CCA415287410NSDHLc.971T>C (p.Phe324Ser)
c.1019T>C (p.Phe340Ser)
Xg.152868965T>GCA415287411NSDHLc.971T>G (p.Phe324Cys)
c.1019T>G (p.Phe340Cys)
Xg.152868966C>ACA415287413NSDHLc.972C>A (p.Phe324Leu)
c.1020C>A (p.Phe340Leu)
 gnomAD v4
Xg.152868966C>GCA415287414NSDHLc.972C>G (p.Phe324Leu)
c.1020C>G (p.Phe340Leu)
Xg.152868966C>TCA519182735NSDHLc.972C>T (p.Phe324=)
c.1020C>T (p.Phe340=)
Xg.152868967A>CCA415287415NSDHLc.973A>C (p.Thr325Pro)
c.1021A>C (p.Thr341Pro)
Xg.152868967A>GCA415287416NSDHLc.973A>G (p.Thr325Ala)
c.1021A>G (p.Thr341Ala)
 ClinVar
Xg.152868967A>TCA415287417NSDHLc.973A>T (p.Thr325Ser)
c.1021A>T (p.Thr341Ser)
Xg.152868968C>ACA415287418NSDHLc.974C>A (p.Thr325Lys)
c.1022C>A (p.Thr341Lys)
Xg.152868968C>GCA415287419NSDHLc.974C>G (p.Thr325Arg)
c.1022C>G (p.Thr341Arg)
Xg.152868968C>TCA415287420NSDHLc.974C>T (p.Thr325Ile)
c.1022C>T (p.Thr341Ile)
Xg.152868969A>CCA519182740NSDHLc.975A>C (p.Thr325=)
c.1023A>C (p.Thr341=)
Xg.152868969A>GCA519182739NSDHLc.975A>G (p.Thr325=)
c.1023A>G (p.Thr341=)
Xg.152868969A>TCA519182738NSDHLc.975A>T (p.Thr325=)
c.1023A>T (p.Thr341=)
Xg.152868970C>ACA415287421NSDHLc.976C>A (p.Pro326Thr)
c.1024C>A (p.Pro342Thr)
Xg.152868970C=CA2466154430NSDHLc.976C= (p.Pro326=)
c.1024C= (p.Pro342=)
Xg.152868970C>GCA415287422NSDHLc.976C>G (p.Pro326Ala)
c.1024C>G (p.Pro342Ala)
 ClinVar
Xg.152868970C>TCA415287423NSDHLc.976C>T (p.Pro326Ser)
c.1024C>T (p.Pro342Ser)
 dbSNP gnomAD v2 gnomAD v4
Xg.152868971C>ACA415287424NSDHLc.977C>A (p.Pro326His)
c.1025C>A (p.Pro342His)
 gnomAD v4
Xg.152868971C>GCA415287426NSDHLc.977C>G (p.Pro326Arg)
c.1025C>G (p.Pro342Arg)
Xg.152868971C>TCA415287425NSDHLc.977C>T (p.Pro326Leu)
c.1025C>T (p.Pro342Leu)
 gnomAD v4
Xg.152868972C>ACA519182741NSDHLc.978C>A (p.Pro326=)
c.1026C>A (p.Pro342=)
Xg.152868972C>GCA519182743NSDHLc.978C>G (p.Pro326=)
c.1026C>G (p.Pro342=)
 gnomAD v4
Xg.152868972C>TCA519182742NSDHLc.978C>T (p.Pro326=)
c.1026C>T (p.Pro342=)
 gnomAD v4
Xg.152868973A=CA2466154431NSDHLc.979A= (p.Met327=)
c.1027A= (p.Met343=)
Xg.152868973A>CCA415287427NSDHLc.979A>C (p.Met327Leu)
c.1027A>C (p.Met343Leu)
Xg.152868973A>GCA415287429NSDHLc.979A>G (p.Met327Val)
c.1027A>G (p.Met343Val)
 ClinVar dbSNP gnomAD v3 gnomAD v4
Xg.152868973A>TCA415287428NSDHLc.979A>T (p.Met327Leu)
c.1027A>T (p.Met343Leu)
Xg.152868974T>ACA415287430NSDHLc.980T>A (p.Met327Lys)
c.1028T>A (p.Met343Lys)
Xg.152868974T>CCA415287431NSDHLc.980T>C (p.Met327Thr)
c.1028T>C (p.Met343Thr)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
Xg.152868974T>GCA415287432NSDHLc.980T>G (p.Met327Arg)
c.1028T>G (p.Met343Arg)
Xg.152868974T=CA2466154432NSDHLc.980T= (p.Met327=)
c.1028T= (p.Met343=)
Xg.152868975G>ACA415287433NSDHLc.981G>A (p.Met327Ile)
c.1029G>A (p.Met343Ile)
 ClinVar gnomAD v4
Xg.152868975G>CCA415287434NSDHLc.981G>C (p.Met327Ile)
c.1029G>C (p.Met343Ile)
Xg.152868975G>TCA415287435NSDHLc.981G>T (p.Met327Ile)
c.1029G>T (p.Met343Ile)
Xg.152868976C>ACA519182746NSDHLc.982C>A (p.Arg328=)
c.1030C>A (p.Arg344=)
Xg.152868976C>GCA415287436NSDHLc.982C>G (p.Arg328Gly)
c.1030C>G (p.Arg344Gly)
Xg.152868976C>TCA415287437NSDHLc.982C>T (p.Arg328Trp)
c.1030C>T (p.Arg344Trp)
 gnomAD v4
Xg.152868977G>ACA415287438NSDHLc.983G>A (p.Arg328Gln)
c.1031G>A (p.Arg344Gln)
 gnomAD v4
Xg.152868977G>CCA415287439NSDHLc.983G>C (p.Arg328Pro)
c.1031G>C (p.Arg344Pro)
Xg.152868977G>TCA415287440NSDHLc.983G>T (p.Arg328Leu)
c.1031G>T (p.Arg344Leu)
Xg.152868978G>ACA519182751NSDHLc.984G>A (p.Arg328=)
c.1032G>A (p.Arg344=)
Xg.152868978G>CCA519182750NSDHLc.984G>C (p.Arg328=)
c.1032G>C (p.Arg344=)
Xg.152868978G>TCA519182752NSDHLc.984G>T (p.Arg328=)
c.1032G>T (p.Arg344=)
Xg.152868979G>ACA415287443NSDHLc.985G>A (p.Val329Ile)
c.1033G>A (p.Val345Ile)
 dbSNP gnomAD v2 gnomAD v4
Xg.152868979G>CCA415287441NSDHLc.985G>C (p.Val329Leu)
c.1033G>C (p.Val345Leu)
Xg.152868979G=CA2466154433NSDHLc.985G= (p.Val329=)
c.1033G= (p.Val345=)
Xg.152868979G>TCA415287442NSDHLc.985G>T (p.Val329Phe)
c.1033G>T (p.Val345Phe)
Xg.152868980T>ACA415287444NSDHLc.986T>A (p.Val329Asp)
c.1034T>A (p.Val345Asp)
Xg.152868980T>CCA415287445NSDHLc.986T>C (p.Val329Ala)
c.1034T>C (p.Val345Ala)
Xg.152868980T>GCA415287446NSDHLc.986T>G (p.Val329Gly)
c.1034T>G (p.Val345Gly)
Xg.152868981C>ACA519182754NSDHLc.987C>A (p.Val329=)
c.1035C>A (p.Val345=)
Xg.152868981C=CA2466154434NSDHLc.987C= (p.Val329=)
c.1035C= (p.Val345=)
Xg.152868981C>GCA519182755NSDHLc.987C>G (p.Val329=)
c.1035C>G (p.Val345=)
Xg.152868981C>TCA10544886NSDHLc.987C>T (p.Val329=)
c.1035C>T (p.Val345=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.152868982G>ACA415287447NSDHLc.988G>A (p.Ala330Thr)
c.1036G>A (p.Ala346Thr)
Xg.152868982G>CCA415287448NSDHLc.988G>C (p.Ala330Pro)
c.1036G>C (p.Ala346Pro)
Xg.152868982G=CA2466154435NSDHLc.988G= (p.Ala330=)
c.1036G= (p.Ala346=)
Xg.152868982G>TCA415287449NSDHLc.988G>T (p.Ala330Ser)
c.1036G>T (p.Ala346Ser)
 dbSNP
Xg.152868983C>ACA415287450NSDHLc.989C>A (p.Ala330Glu)
c.1037C>A (p.Ala346Glu)
Xg.152868983C>GCA415287451NSDHLc.989C>G (p.Ala330Gly)
c.1037C>G (p.Ala346Gly)
Xg.152868983C>TCA415287452NSDHLc.989C>T (p.Ala330Val)
c.1037C>T (p.Ala346Val)
Xg.152868984A=CA2466154436NSDHLc.990A= (p.Ala330=)
c.1038A= (p.Ala346=)
Xg.152868984A>CCA519182760NSDHLc.990A>C (p.Ala330=)
c.1038A>C (p.Ala346=)
Xg.152868984A>GCA337613790NSDHLc.990A>G (p.Ala330=)
c.1038A>G (p.Ala346=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.152868984A>TCA519182759NSDHLc.990A>T (p.Ala330=)
c.1038A>T (p.Ala346=)
Xg.152868985C>ACA415287454NSDHLc.991C>A (p.Leu331Met)
c.1039C>A (p.Leu347Met)
Xg.152868985C=CA2466154437NSDHLc.991C= (p.Leu331=)
c.1039C= (p.Leu347=)
Xg.152868985C>GCA415287453NSDHLc.991C>G (p.Leu331Val)
c.1039C>G (p.Leu347Val)
Xg.152868985C>TCA10544887NSDHLc.991C>T (p.Leu331=)
c.1039C>T (p.Leu347=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.152868986T>ACA415287455NSDHLc.992T>A (p.Leu331Gln)
c.1040T>A (p.Leu347Gln)
Xg.152868986T>CCA415287456NSDHLc.992T>C (p.Leu331Pro)
c.1040T>C (p.Leu347Pro)
Xg.152868986T>GCA415287457NSDHLc.992T>G (p.Leu331Arg)
c.1040T>G (p.Leu347Arg)
Xg.152868987G>ACA519182765NSDHLc.993G>A (p.Leu331=)
c.1041G>A (p.Leu347=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.152868987G>CCA519182766NSDHLc.993G>C (p.Leu331=)
c.1041G>C (p.Leu347=)
Xg.152868987G=CA2466154438NSDHLc.993G= (p.Leu331=)
c.1041G= (p.Leu347=)
Xg.152868987G>TCA519182767NSDHLc.993G>T (p.Leu331=)
c.1041G>T (p.Leu347=)
Xg.152868988G>ACA415287458NSDHLc.994G>A (p.Ala332Thr)
c.1042G>A (p.Ala348Thr)
Xg.152868988G>CCA415287459NSDHLc.994G>C (p.Ala332Pro)
c.1042G>C (p.Ala348Pro)
Xg.152868988G>TCA415287460NSDHLc.994G>T (p.Ala332Ser)
c.1042G>T (p.Ala348Ser)
Xg.152868989C>ACA415287461NSDHLc.995C>A (p.Ala332Asp)
c.1043C>A (p.Ala348Asp)
Xg.152868989C>GCA415287462NSDHLc.995C>G (p.Ala332Gly)
c.1043C>G (p.Ala348Gly)
 gnomAD v4 COSMIC
Xg.152868989C>TCA415287463NSDHLc.995C>T (p.Ala332Val)
c.1043C>T (p.Ala348Val)
Xg.152868990T>ACA519182768NSDHLc.996T>A (p.Ala332=)
c.1044T>A (p.Ala348=)
Xg.152868990T>CCA519182769NSDHLc.996T>C (p.Ala332=)
c.1044T>C (p.Ala348=)
 COSMIC
Xg.152868990T>GCA519182771NSDHLc.996T>G (p.Ala332=)
c.1044T>G (p.Ala348=)
Xg.152868991G>ACA10544888NSDHLc.997G>A (p.Gly333Ser)
c.1045G>A (p.Gly349Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.152868991G>CCA415287465NSDHLc.997G>C (p.Gly333Arg)
c.1045G>C (p.Gly349Arg)
Xg.152868991G=CA2466154439NSDHLc.997G= (p.Gly333=)
c.1045G= (p.Gly349=)
Xg.152868991G>TCA415287464NSDHLc.997G>T (p.Gly333Cys)
c.1045G>T (p.Gly349Cys)
Xg.152868992G>ACA415287466NSDHLc.998G>A (p.Gly333Asp)
c.1046G>A (p.Gly349Asp)
Xg.152868992G>CCA415287467NSDHLc.998G>C (p.Gly333Ala)
c.1046G>C (p.Gly349Ala)
Xg.152868992G>TCA415287468NSDHLc.998G>T (p.Gly333Val)
c.1046G>T (p.Gly349Val)
Xg.152868993C>ACA519182778NSDHLc.999C>A (p.Gly333=)
c.1047C>A (p.Gly349=)
Xg.152868993C>GCA519182779NSDHLc.999C>G (p.Gly333=)
c.1047C>G (p.Gly349=)
Xg.152868993C>TCA519182780NSDHLc.999C>T (p.Gly333=)
c.1047C>T (p.Gly349=)
Xg.152868994A>CCA415287469NSDHLc.1000A>C (p.Thr334Pro)
c.1048A>C (p.Thr350Pro)
Xg.152868994A>GCA415287470NSDHLc.1000A>G (p.Thr334Ala)
c.1048A>G (p.Thr350Ala)
Xg.152868994A>TCA415287471NSDHLc.1000A>T (p.Thr334Ser)
c.1048A>T (p.Thr350Ser)
Xg.152868995C>ACA415287472NSDHLc.1001C>A (p.Thr334Lys)
c.1049C>A (p.Thr350Lys)
Xg.152868995C=CA2466154440NSDHLc.1001C= (p.Thr334=)
c.1049C= (p.Thr350=)
Xg.152868995C>GCA415287473NSDHLc.1001C>G (p.Thr334Arg)
c.1049C>G (p.Thr350Arg)
 dbSNP gnomAD v4
Xg.152868995C>TCA415287474NSDHLc.1001C>T (p.Thr334Ile)
c.1049C>T (p.Thr350Ile)
 dbSNP
Xg.152868996A>CCA519182785NSDHLc.1002A>C (p.Thr334=)
c.1050A>C (p.Thr350=)
Xg.152868996A>GCA519182787NSDHLc.1002A>G (p.Thr334=)
c.1050A>G (p.Thr350=)
 gnomAD v4
Xg.152868996A>TCA519182789NSDHLc.1002A>T (p.Thr334=)
c.1050A>T (p.Thr350=)
Xg.152868997T>ACA415287475NSDHLc.1003T>A (p.Phe335Ile)
c.1051T>A (p.Phe351Ile)
Xg.152868997T>CCA415287476NSDHLc.1003T>C (p.Phe335Leu)
c.1051T>C (p.Phe351Leu)
Xg.152868997T>GCA415287477NSDHLc.1003T>G (p.Phe335Val)
c.1051T>G (p.Phe351Val)
Xg.152868998T>ACA415287479NSDHLc.1004T>A (p.Phe335Tyr)
c.1052T>A (p.Phe351Tyr)
Xg.152868998T>CCA415287480NSDHLc.1004T>C (p.Phe335Ser)
c.1052T>C (p.Phe351Ser)
Xg.152868998T>GCA415287478NSDHLc.1004T>G (p.Phe335Cys)
c.1052T>G (p.Phe351Cys)
Xg.152868999C>ACA415287482NSDHLc.1005C>A (p.Phe335Leu)
c.1053C>A (p.Phe351Leu)
Xg.152868999C=CA2466154441NSDHLc.1005C= (p.Phe335=)
c.1053C= (p.Phe351=)
Xg.152868999C>GCA415287481NSDHLc.1005C>G (p.Phe335Leu)
c.1053C>G (p.Phe351Leu)
 dbSNP gnomAD v3 gnomAD v4
Xg.152868999C>TCA519182791NSDHLc.1005C>T (p.Phe335=)
c.1053C>T (p.Phe351=)
Xg.152869000C>ACA415287484NSDHLc.1006C>A (p.His336Asn)
c.1054C>A (p.His352Asn)
Xg.152869000C>GCA415287483NSDHLc.1006C>G (p.His336Asp)
c.1054C>G (p.His352Asp)
Xg.152869000C>TCA415287485NSDHLc.1006C>T (p.His336Tyr)
c.1054C>T (p.His352Tyr)
 COSMIC
Xg.152869001A>CCA415287486NSDHLc.1007A>C (p.His336Pro)
c.1055A>C (p.His352Pro)
Xg.152869001A>GCA415287487NSDHLc.1007A>G (p.His336Arg)
c.1055A>G (p.His352Arg)
Xg.152869001A>TCA415287488NSDHLc.1007A>T (p.His336Leu)
c.1055A>T (p.His352Leu)
Xg.152869002C>ACA415287489NSDHLc.1008C>A (p.His336Gln)
c.1056C>A (p.His352Gln)
Xg.152869002C=CA2466154442NSDHLc.1008C= (p.His336=)
c.1056C= (p.His352=)
Xg.152869002C>GCA415287490NSDHLc.1008C>G (p.His336Gln)
c.1056C>G (p.His352Gln)
Xg.152869002C>TCA519182792NSDHLc.1008C>T (p.His336=)
c.1056C>T (p.His352=)
 dbSNP
Xg.152869003T>ACA415287491NSDHLc.1009T>A (p.Tyr337Asn)
c.1057T>A (p.Tyr353Asn)
Xg.152869003T>CCA415287492NSDHLc.1009T>C (p.Tyr337His)
c.1057T>C (p.Tyr353His)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.152869003T>GCA415287493NSDHLc.1009T>G (p.Tyr337Asp)
c.1057T>G (p.Tyr353Asp)
Xg.152869003T=CA2466154443NSDHLc.1009T= (p.Tyr337=)
c.1057T= (p.Tyr353=)
Xg.152869004A=CA2466154444NSDHLc.1010A= (p.Tyr337=)
c.1058A= (p.Tyr353=)
Xg.152869004A>CCA415287494NSDHLc.1010A>C (p.Tyr337Ser)
c.1058A>C (p.Tyr353Ser)
Xg.152869004A>GCA415287495NSDHLc.1010A>G (p.Tyr337Cys)
c.1058A>G (p.Tyr353Cys)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.152869004A>TCA415287496NSDHLc.1010A>T (p.Tyr337Phe)
c.1058A>T (p.Tyr353Phe)
 gnomAD v4
Xg.152869005C>ACA415287497NSDHLc.1011C>A (p.Tyr337Ter)
c.1059C>A (p.Tyr353Ter)
Xg.152869005C>GCA415287498NSDHLc.1011C>G (p.Tyr337Ter)
c.1059C>G (p.Tyr353Ter)
Xg.152869005C>TCA519182794NSDHLc.1011C>T (p.Tyr337=)
c.1059C>T (p.Tyr353=)
Xg.152869006T>ACA415287501NSDHLc.1012T>A (p.Tyr338Asn)
c.1060T>A (p.Tyr354Asn)
Xg.152869006T>CCA415287499NSDHLc.1012T>C (p.Tyr338His)
c.1060T>C (p.Tyr354His)
Xg.152869006T>GCA415287500NSDHLc.1012T>G (p.Tyr338Asp)
c.1060T>G (p.Tyr354Asp)
Xg.152869007A>CCA415287502NSDHLc.1013A>C (p.Tyr338Ser)
c.1061A>C (p.Tyr354Ser)
Xg.152869007A>GCA415287503NSDHLc.1013A>G (p.Tyr338Cys)
c.1061A>G (p.Tyr354Cys)
Xg.152869007A>TCA415287504NSDHLc.1013A>T (p.Tyr338Phe)
c.1061A>T (p.Tyr354Phe)
Xg.152869008C>ACA415287505NSDHLc.1014C>A (p.Tyr338Ter)
c.1062C>A (p.Tyr354Ter)
Xg.152869008C>GCA415287506NSDHLc.1014C>G (p.Tyr338Ter)
c.1062C>G (p.Tyr354Ter)
Xg.152869008C>TCA519182799NSDHLc.1014C>T (p.Tyr338=)
c.1062C>T (p.Tyr354=)
Xg.152869009A>CCA415287507NSDHLc.1015A>C (p.Ser339Arg)
c.1063A>C (p.Ser355Arg)
Xg.152869009A>GCA415287508NSDHLc.1015A>G (p.Ser339Gly)
c.1063A>G (p.Ser355Gly)
Xg.152869009A>TCA415287509NSDHLc.1015A>T (p.Ser339Cys)
c.1063A>T (p.Ser355Cys)
Xg.152869010G>ACA415287510NSDHLc.1016G>A (p.Ser339Asn)
c.1064G>A (p.Ser355Asn)
Xg.152869010G>CCA415287511NSDHLc.1016G>C (p.Ser339Thr)
c.1064G>C (p.Ser355Thr)
Xg.152869010G>TCA415287512NSDHLc.1016G>T (p.Ser339Ile)
c.1064G>T (p.Ser355Ile)
Xg.152869011C>ACA415287513NSDHLc.1017C>A (p.Ser339Arg)
c.1065C>A (p.Ser355Arg)
Xg.152869011C=CA2466154445NSDHLc.1017C= (p.Ser339=)
c.1065C= (p.Ser355=)
Xg.152869011C>GCA415287514NSDHLc.1017C>G (p.Ser339Arg)
c.1065C>G (p.Ser355Arg)
Xg.152869011C>TCA10544889NSDHLc.1017C>T (p.Ser339=)
c.1065C>T (p.Ser355=)
 dbSNP ExAC gnomAD v2 gnomAD v4
Xg.152869012T>ACA415287515NSDHLc.1018T>A (p.Cys340Ser)
c.1066T>A (p.Cys356Ser)
Xg.152869012T>CCA415287516NSDHLc.1018T>C (p.Cys340Arg)
c.1066T>C (p.Cys356Arg)
Xg.152869012T>GCA415287517NSDHLc.1018T>G (p.Cys340Gly)
c.1066T>G (p.Cys356Gly)
Xg.152869013G>ACA415287518NSDHLc.1019G>A (p.Cys340Tyr)
c.1067G>A (p.Cys356Tyr)
Xg.152869013G>CCA415287519NSDHLc.1019G>C (p.Cys340Ser)
c.1067G>C (p.Cys356Ser)
Xg.152869013G>TCA415287520NSDHLc.1019G>T (p.Cys340Phe)
c.1067G>T (p.Cys356Phe)
Xg.152869014C>ACA415287521NSDHLc.1020C>A (p.Cys340Ter)
c.1068C>A (p.Cys356Ter)
Xg.152869014C=CA2466154446NSDHLc.1020C= (p.Cys340=)
c.1068C= (p.Cys356=)
Xg.152869014C>GCA415287522NSDHLc.1020C>G (p.Cys340Trp)
c.1068C>G (p.Cys356Trp)
Xg.152869014C>TCA10544890NSDHLc.1020C>T (p.Cys340=)
c.1068C>T (p.Cys356=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.152869015G>ACA10544891NSDHLc.1021G>A (p.Glu341Lys)
c.1069G>A (p.Glu357Lys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
Xg.152869015G>CCA415287523NSDHLc.1021G>C (p.Glu341Gln)
c.1069G>C (p.Glu357Gln)
Xg.152869015G=CA2466154447NSDHLc.1021G= (p.Glu341=)
c.1069G= (p.Glu357=)
Xg.152869015G>TCA415287524NSDHLc.1021G>T (p.Glu341Ter)
c.1069G>T (p.Glu357Ter)
Xg.152869016A>CCA415287525NSDHLc.1022A>C (p.Glu341Ala)
c.1070A>C (p.Glu357Ala)
Xg.152869016A>GCA415287527NSDHLc.1022A>G (p.Glu341Gly)
c.1070A>G (p.Glu357Gly)
Xg.152869016A>TCA415287526NSDHLc.1022A>T (p.Glu341Val)
c.1070A>T (p.Glu357Val)
Xg.152869017G>ACA519182815NSDHLc.1023G>A (p.Glu341=)
c.1071G>A (p.Glu357=)
 gnomAD v4
Xg.152869017G>CCA415287528NSDHLc.1023G>C (p.Glu341Asp)
c.1071G>C (p.Glu357Asp)
Xg.152869017G>TCA415287529NSDHLc.1023G>T (p.Glu341Asp)
c.1071G>T (p.Glu357Asp)
Xg.152869018A>CCA519182817NSDHLc.1024A>C (p.Arg342=)
c.1072A>C (p.Arg358=)
Xg.152869018A>GCA415287530NSDHLc.1024A>G (p.Arg342Gly)
c.1072A>G (p.Arg358Gly)
Xg.152869018A>TCA415287531NSDHLc.1024A>T (p.Arg342Ter)
c.1072A>T (p.Arg358Ter)
Xg.152869019G>ACA415287532NSDHLc.1025G>A (p.Arg342Lys)
c.1073G>A (p.Arg358Lys)
 gnomAD v4
Xg.152869019G>CCA415287533NSDHLc.1025G>C (p.Arg342Thr)
c.1073G>C (p.Arg358Thr)
Xg.152869019G>TCA415287534NSDHLc.1025G>T (p.Arg342Ile)
c.1073G>T (p.Arg358Ile)
Xg.152869020A=CA2466154448NSDHLc.1026A= (p.Arg342=)
c.1074A= (p.Arg358=)
Xg.152869020A>CCA415287535NSDHLc.1026A>C (p.Arg342Ser)
c.1074A>C (p.Arg358Ser)
Xg.152869020A>GCA519182818NSDHLc.1026A>G (p.Arg342=)
c.1074A>G (p.Arg358=)
Xg.152869020A>TCA415287536NSDHLc.1026A>T (p.Arg342Ser)
c.1074A>T (p.Arg358Ser)
 dbSNP gnomAD v2 gnomAD v4
Xg.152869021G>ACA415287539NSDHLc.1027G>A (p.Ala343Thr)
c.1075G>A (p.Ala359Thr)
Xg.152869021G>CCA415287538NSDHLc.1027G>C (p.Ala343Pro)
c.1075G>C (p.Ala359Pro)
Xg.152869021G>TCA415287537NSDHLc.1027G>T (p.Ala343Ser)
c.1075G>T (p.Ala359Ser)
Xg.152869022C>ACA415287540NSDHLc.1028C>A (p.Ala343Asp)
c.1076C>A (p.Ala359Asp)
Xg.152869022C>GCA415287541NSDHLc.1028C>G (p.Ala343Gly)
c.1076C>G (p.Ala359Gly)
Xg.152869022C>TCA415287542NSDHLc.1028C>T (p.Ala343Val)
c.1076C>T (p.Ala359Val)
Xg.152869023C>ACA519182825NSDHLc.1029C>A (p.Ala343=)
c.1077C>A (p.Ala359=)
Xg.152869023C=CA2466154449NSDHLc.1029C= (p.Ala343=)
c.1077C= (p.Ala359=)
Xg.152869023C>GCA519182826NSDHLc.1029C>G (p.Ala343=)
c.1077C>G (p.Ala359=)
Xg.152869023C>TCA519182824NSDHLc.1029C>T (p.Ala343=)
c.1077C>T (p.Ala359=)
 dbSNP
Xg.152869024A>CCA415287543NSDHLc.1030A>C (p.Lys344Gln)
c.1078A>C (p.Lys360Gln)
Xg.152869024A>GCA415287544NSDHLc.1030A>G (p.Lys344Glu)
c.1078A>G (p.Lys360Glu)
 gnomAD v4
Xg.152869024A>TCA415287545NSDHLc.1030A>T (p.Lys344Ter)
c.1078A>T (p.Lys360Ter)
Xg.152869025A>CCA415287546NSDHLc.1031A>C (p.Lys344Thr)
c.1079A>C (p.Lys360Thr)
Xg.152869025A>GCA415287547NSDHLc.1031A>G (p.Lys344Arg)
c.1079A>G (p.Lys360Arg)
 ClinVar dbSNP gnomAD v4
Xg.152869025A>TCA415287548NSDHLc.1031A>T (p.Lys344Ile)
c.1079A>T (p.Lys360Ile)
Xg.152869026A=CA2466154450NSDHLc.1032A= (p.Lys344=)
c.1080A= (p.Lys360=)
Xg.152869026A>CCA415287549NSDHLc.1032A>C (p.Lys344Asn)
c.1080A>C (p.Lys360Asn)
Xg.152869026A>GCA10544892NSDHLc.1032A>G (p.Lys344=)
c.1080A>G (p.Lys360=)
 dbSNP ExAC gnomAD v2 gnomAD v4
Xg.152869026A>TCA415287550NSDHLc.1032A>T (p.Lys344Asn)
c.1080A>T (p.Lys360Asn)
Xg.152869027A>CCA415287553NSDHLc.1033A>C (p.Lys345Gln)
c.1081A>C (p.Lys361Gln)
Xg.152869027A>GCA415287552NSDHLc.1033A>G (p.Lys345Glu)
c.1081A>G (p.Lys361Glu)
Xg.152869027A>TCA415287551NSDHLc.1033A>T (p.Lys345Ter)
c.1081A>T (p.Lys361Ter)
Xg.152869028A>CCA415287554NSDHLc.1034A>C (p.Lys345Thr)
c.1082A>C (p.Lys361Thr)
Xg.152869028A>GCA415287555NSDHLc.1034A>G (p.Lys345Arg)
c.1082A>G (p.Lys361Arg)
Xg.152869028A>TCA415287556NSDHLc.1034A>T (p.Lys345Met)
c.1082A>T (p.Lys361Met)
Xg.152869029G>ACA519182831NSDHLc.1035G>A (p.Lys345=)
c.1083G>A (p.Lys361=)
Xg.152869029G>CCA415287557NSDHLc.1035G>C (p.Lys345Asn)
c.1083G>C (p.Lys361Asn)
Xg.152869029G>TCA415287558NSDHLc.1035G>T (p.Lys345Asn)
c.1083G>T (p.Lys361Asn)
Xg.152869030G>ACA415287559NSDHLc.1036G>A (p.Ala346Thr)
c.1084G>A (p.Ala362Thr)
 dbSNP
Xg.152869030G>CCA415287560NSDHLc.1036G>C (p.Ala346Pro)
c.1084G>C (p.Ala362Pro)
Xg.152869030G=CA2466154451NSDHLc.1036G= (p.Ala346=)
c.1084G= (p.Ala362=)
Xg.152869030G>TCA415287561NSDHLc.1036G>T (p.Ala346Ser)
c.1084G>T (p.Ala362Ser)
Xg.152869031C>ACA415287562NSDHLc.1037C>A (p.Ala346Asp)
c.1085C>A (p.Ala362Asp)
 ClinVar
Xg.152869031C=CA2466154452NSDHLc.1037C= (p.Ala346=)
c.1085C= (p.Ala362=)
Xg.152869031C>GCA415287563NSDHLc.1037C>G (p.Ala346Gly)
c.1085C>G (p.Ala362Gly)
 ClinVar dbSNP gnomAD v4
Xg.152869031C>TCA10544893NSDHLc.1037C>T (p.Ala346Val)
c.1085C>T (p.Ala362Val)
 dbSNP ExAC gnomAD v2 gnomAD v4
Xg.152869032C>ACA519182835NSDHLc.1038C>A (p.Ala346=)
c.1086C>A (p.Ala362=)
Xg.152869032C=CA2466154453NSDHLc.1038C= (p.Ala346=)
c.1086C= (p.Ala362=)
Xg.152869032C>GCA519182833NSDHLc.1038C>G (p.Ala346=)
c.1086C>G (p.Ala362=)
Xg.152869032C>TCA519182834NSDHLc.1038C>T (p.Ala346=)
c.1086C>T (p.Ala362=)
 dbSNP gnomAD v2 gnomAD v4
Xg.152869032_152869035dupCA276997NSDHLc.1038_1041dup (p.Gly348HisfsTer11)
c.1086_1089dup (p.Gly364HisfsTer11)
 ClinVar dbSNP
Xg.152869033A=CA2466154454NSDHLc.1039A= (p.Met347=)
c.1087A= (p.Met363=)
Xg.152869033A>CCA415287564NSDHLc.1039A>C (p.Met347Leu)
c.1087A>C (p.Met363Leu)
Xg.152869033A>GCA415287566NSDHLc.1039A>G (p.Met347Val)
c.1087A>G (p.Met363Val)
 dbSNP
Xg.152869033A>TCA415287565NSDHLc.1039A>T (p.Met347Leu)
c.1087A>T (p.Met363Leu)
Xg.152869034T>ACA415287567NSDHLc.1040T>A (p.Met347Lys)
c.1088T>A (p.Met363Lys)
Xg.152869034T>CCA415287568NSDHLc.1040T>C (p.Met347Thr)
c.1088T>C (p.Met363Thr)
Xg.152869034T>GCA10544894NSDHLc.1040T>G (p.Met347Arg)
c.1088T>G (p.Met363Arg)
 dbSNP ExAC
Xg.152869034T=CA2466154455NSDHLc.1040T= (p.Met347=)
c.1088T= (p.Met363=)
Xg.152869035G>ACA415287569NSDHLc.1041G>A (p.Met347Ile)
c.1089G>A (p.Met363Ile)
Xg.152869035G>CCA415287570NSDHLc.1041G>C (p.Met347Ile)
c.1089G>C (p.Met363Ile)
Xg.152869035G>TCA415287571NSDHLc.1041G>T (p.Met347Ile)
c.1089G>T (p.Met363Ile)
Xg.152869036G>ACA415287572NSDHLc.1042G>A (p.Gly348Ser)
c.1090G>A (p.Gly364Ser)
Xg.152869036G>CCA415287573NSDHLc.1042G>C (p.Gly348Arg)
c.1090G>C (p.Gly364Arg)
Xg.152869036G>TCA415287574NSDHLc.1042G>T (p.Gly348Cys)
c.1090G>T (p.Gly364Cys)
Xg.152869037G>ACA415287575NSDHLc.1043G>A (p.Gly348Asp)
c.1091G>A (p.Gly364Asp)
 dbSNP gnomAD v2 gnomAD v4 COSMIC
Xg.152869037G>CCA10544896NSDHLc.1043G>C (p.Gly348Ala)
c.1091G>C (p.Gly364Ala)
 dbSNP ExAC gnomAD v2
Xg.152869037G=CA2466154456NSDHLc.1043G= (p.Gly348=)
c.1091G= (p.Gly364=)
Xg.152869037G>TCA10544895NSDHLc.1043G>T (p.Gly348Val)
c.1091G>T (p.Gly364Val)
 dbSNP ExAC

Number of alleles fetched