Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.38581089T>ACA352139621SCN5Ac.3070A>T (p.Lys1024Ter)
c.2941A>T (p.Lys981Ter)
dbSNP
3g.38581089T>CCA352139623SCN5Ac.3070A>G (p.Lys1024Glu)
c.2941A>G (p.Lys981Glu)
dbSNP
3g.38581089T>GCA352139625SCN5Ac.3070A>C (p.Lys1024Gln)
c.2941A>C (p.Lys981Gln)
3g.38581089T=CA1358574297SCN5Ac.3070A= (p.Lys1024=)
c.2941A= (p.Lys981=)
3g.38581090G>ACA433135412SCN5Ac.3069C>T (p.Arg1023=)
c.2940C>T (p.Arg980=)
3g.38581090G>CCA433135415SCN5Ac.3069C>G (p.Arg1023=)
c.2940C>G (p.Arg980=)
3g.38581090G>TCA433135418SCN5Ac.3069C>A (p.Arg1023=)
c.2940C>A (p.Arg980=)
3g.38581091C>ACA352139627SCN5Ac.3068G>T (p.Arg1023Leu)
c.2939G>T (p.Arg980Leu)
ClinVar gnomAD v4
3g.38581091C=CA1358574305SCN5Ac.3068G= (p.Arg1023=)
c.2939G= (p.Arg980=)
3g.38581091C>GCA061242SCN5Ac.3068G>C (p.Arg1023Pro)
c.2939G>C (p.Arg980Pro)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38581091C>TCA016787SCN5Ac.3068G>A (p.Arg1023His)
c.2939G>A (p.Arg980His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38581092G>ACA061233SCN5Ac.3067C>T (p.Arg1023Cys)
c.2938C>T (p.Arg980Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC
3g.38581092G>CCA352139633SCN5Ac.3067C>G (p.Arg1023Gly)
c.2938C>G (p.Arg980Gly)
ClinVar
3g.38581092G=CA1358574313SCN5Ac.3067C= (p.Arg1023=)
c.2938C= (p.Arg980=)
3g.38581092G>TCA352139631SCN5Ac.3067C>A (p.Arg1023Ser)
c.2938C>A (p.Arg980Ser)
dbSNP
3g.38581093G>ACA433135425SCN5Ac.3066C>T (p.Thr1022=)
c.2937C>T (p.Thr979=)
3g.38581093G>CCA433135426SCN5Ac.3066C>G (p.Thr1022=)
c.2937C>G (p.Thr979=)
3g.38581093G>TCA433135429SCN5Ac.3066C>A (p.Thr1022=)
c.2937C>A (p.Thr979=)
3g.38581094G>ACA352139636SCN5Ac.3065C>T (p.Thr1022Ile)
c.2936C>T (p.Thr979Ile)
gnomAD v4
3g.38581094G>CCA352139641SCN5Ac.3065C>G (p.Thr1022Ser)
c.2936C>G (p.Thr979Ser)
3g.38581094G=CA1358574322SCN5Ac.3065C= (p.Thr1022=)
c.2936C= (p.Thr979=)
3g.38581094G>TCA352139638SCN5Ac.3065C>A (p.Thr1022Asn)
c.2936C>A (p.Thr979Asn)
ClinVar dbSNP gnomAD v4
3g.38581095T>ACA352139643SCN5Ac.3064A>T (p.Thr1022Ser)
c.2935A>T (p.Thr979Ser)
3g.38581095T>CCA352139644SCN5Ac.3064A>G (p.Thr1022Ala)
c.2935A>G (p.Thr979Ala)
ClinVar dbSNP gnomAD v4
3g.38581095T>GCA352139646SCN5Ac.3064A>C (p.Thr1022Pro)
c.2935A>C (p.Thr979Pro)
3g.38581095T=CA1358574325SCN5Ac.3064A= (p.Thr1022=)
c.2935A= (p.Thr979=)
3g.38581096G>ACA433135436SCN5Ac.3063C>T (p.Pro1021=)
c.2934C>T (p.Pro978=)
3g.38581096G>CCA061228SCN5Ac.3063C>G (p.Pro1021=)
c.2934C>G (p.Pro978=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38581096G=CA1358574328SCN5Ac.3063C= (p.Pro1021=)
c.2934C= (p.Pro978=)
3g.38581096G>TCA433135438SCN5Ac.3063C>A (p.Pro1021=)
c.2934C>A (p.Pro978=)
3g.38581097G>ACA352139650SCN5Ac.3062C>T (p.Pro1021Leu)
c.2933C>T (p.Pro978Leu)
3g.38581097G>CCA352139651SCN5Ac.3062C>G (p.Pro1021Arg)
c.2933C>G (p.Pro978Arg)
3g.38581097G>TCA352139653SCN5Ac.3062C>A (p.Pro1021His)
c.2933C>A (p.Pro978His)
3g.38581098G>ACA016779SCN5Ac.3061C>T (p.Pro1021Ser)
c.2932C>T (p.Pro978Ser)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC
3g.38581098G>CCA352139656SCN5Ac.3061C>G (p.Pro1021Ala)
c.2932C>G (p.Pro978Ala)
3g.38581098G=CA1358574332SCN5Ac.3061C= (p.Pro1021=)
c.2932C= (p.Pro978=)
3g.38581098G>TCA352139658SCN5Ac.3061C>A (p.Pro1021Thr)
c.2932C>A (p.Pro978Thr)
3g.38581099A>CCA433135451SCN5Ac.3060T>G (p.Pro1020=)
c.2931T>G (p.Pro977=)
3g.38581099A>GCA433135452SCN5Ac.3060T>C (p.Pro1020=)
c.2931T>C (p.Pro977=)
3g.38581099A>TCA433135449SCN5Ac.3060T>A (p.Pro1020=)
c.2931T>A (p.Pro977=)
3g.38581100G>ACA352139663SCN5Ac.3059C>T (p.Pro1020Leu)
c.2930C>T (p.Pro977Leu)
ClinVar dbSNP
3g.38581100G>CCA352139661SCN5Ac.3059C>G (p.Pro1020Arg)
c.2930C>G (p.Pro977Arg)
3g.38581100G=CA1358574336SCN5Ac.3059C= (p.Pro1020=)
c.2930C= (p.Pro977=)
3g.38581100G>TCA352139660SCN5Ac.3059C>A (p.Pro1020His)
c.2930C>A (p.Pro977His)
3g.38581101G>ACA352139665SCN5Ac.3058C>T (p.Pro1020Ser)
c.2929C>T (p.Pro977Ser)
ClinVar dbSNP
3g.38581101G>CCA352139669SCN5Ac.3058C>G (p.Pro1020Ala)
c.2929C>G (p.Pro977Ala)
3g.38581101G=CA1358574338SCN5Ac.3058C= (p.Pro1020=)
c.2929C= (p.Pro977=)
3g.38581101G>TCA352139671SCN5Ac.3058C>A (p.Pro1020Thr)
c.2929C>A (p.Pro977Thr)
3g.38581102C>ACA433135465SCN5Ac.3057G>T (p.Val1019=)
c.2928G>T (p.Val976=)
gnomAD v4
3g.38581102C=CA1358574342SCN5Ac.3057G= (p.Val1019=)
c.2928G= (p.Val976=)
3g.38581102C>GCA433135461SCN5Ac.3057G>C (p.Val1019=)
c.2928G>C (p.Val976=)
3g.38581102C>TCA061223SCN5Ac.3057G>A (p.Val1019=)
c.2928G>A (p.Val976=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38581103A=CA1358574345SCN5Ac.3056T= (p.Val1019=)
c.2927T= (p.Val976=)
3g.38581103A>CCA352139675SCN5Ac.3056T>G (p.Val1019Gly)
c.2927T>G (p.Val976Gly)
dbSNP
3g.38581103A>GCA352139676SCN5Ac.3056T>C (p.Val1019Ala)
c.2927T>C (p.Val976Ala)
dbSNP
3g.38581103A>TCA352139678SCN5Ac.3056T>A (p.Val1019Glu)
c.2927T>A (p.Val976Glu)
ClinVar
3g.38581104C>ACA352139681SCN5Ac.3055G>T (p.Val1019Leu)
c.2926G>T (p.Val976Leu)
3g.38581104C>GCA352139682SCN5Ac.3055G>C (p.Val1019Leu)
c.2926G>C (p.Val976Leu)
3g.38581104C>TCA352139684SCN5Ac.3055G>A (p.Val1019Met)
c.2926G>A (p.Val976Met)
3g.38581105C>ACA352139686SCN5Ac.3054G>T (p.Lys1018Asn)
c.2925G>T (p.Lys975Asn)
3g.38581105C=CA1358574347SCN5Ac.3054G= (p.Lys1018=)
c.2925G= (p.Lys975=)
3g.38581105C>GCA352139688SCN5Ac.3054G>C (p.Lys1018Asn)
c.2925G>C (p.Lys975Asn)
3g.38581105C>TCA433135472SCN5Ac.3054G>A (p.Lys1018=)
c.2925G>A (p.Lys975=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.38581106T>ACA352139693SCN5Ac.3053A>T (p.Lys1018Met)
c.2924A>T (p.Lys975Met)
3g.38581106T>CCA352139694SCN5Ac.3053A>G (p.Lys1018Arg)
c.2924A>G (p.Lys975Arg)
3g.38581106T>GCA352139691SCN5Ac.3053A>C (p.Lys1018Thr)
c.2924A>C (p.Lys975Thr)
gnomAD v4
3g.38581107T>ACA352139697SCN5Ac.3052A>T (p.Lys1018Ter)
c.2923A>T (p.Lys975Ter)
ClinVar dbSNP
3g.38581107T>CCA061220SCN5Ac.3052A>G (p.Lys1018Glu)
c.2923A>G (p.Lys975Glu)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.38581107T>GCA352139700SCN5Ac.3052A>C (p.Lys1018Gln)
c.2923A>C (p.Lys975Gln)
3g.38581107T=CA1358574350SCN5Ac.3052A= (p.Lys1018=)
c.2923A= (p.Lys975=)
3g.38581108C>ACA352139702SCN5Ac.3051G>T (p.Glu1017Asp)
c.2922G>T (p.Glu974Asp)
3g.38581108C>GCA352139704SCN5Ac.3051G>C (p.Glu1017Asp)
c.2922G>C (p.Glu974Asp)
3g.38581108C>TCA433135480SCN5Ac.3051G>A (p.Glu1017=)
c.2922G>A (p.Glu974=)
COSMIC COSMIC COSMIC
3g.38581109T>ACA352139706SCN5Ac.3050A>T (p.Glu1017Val)
c.2921A>T (p.Glu974Val)
3g.38581109T>CCA352139707SCN5Ac.3050A>G (p.Glu1017Gly)
c.2921A>G (p.Glu974Gly)
gnomAD v4
3g.38581109T>GCA352139709SCN5Ac.3050A>C (p.Glu1017Ala)
c.2921A>C (p.Glu974Ala)
3g.38581110C>ACA352139711SCN5Ac.3049G>T (p.Glu1017Ter)
c.2920G>T (p.Glu974Ter)
dbSNP
3g.38581110C=CA1358574354SCN5Ac.3049G= (p.Glu1017=)
c.2920G= (p.Glu974=)
3g.38581110C>GCA352139712SCN5Ac.3049G>C (p.Glu1017Gln)
c.2920G>C (p.Glu974Gln)
3g.38581110C>TCA352139714SCN5Ac.3049G>A (p.Glu1017Lys)
c.2920G>A (p.Glu974Lys)
COSMIC COSMIC COSMIC
3g.38581111C>ACA433135487SCN5Ac.3048G>T (p.Thr1016=)
c.2919G>T (p.Thr973=)
3g.38581111C=CA1358574357SCN5Ac.3048G= (p.Thr1016=)
c.2919G= (p.Thr973=)
3g.38581111C>GCA433135488SCN5Ac.3048G>C (p.Thr1016=)
c.2919G>C (p.Thr973=)
3g.38581111C>TCA016770SCN5Ac.3048G>A (p.Thr1016=)
c.2919G>A (p.Thr973=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38581112G>ACA016763SCN5Ac.3047C>T (p.Thr1016Met)
c.2918C>T (p.Thr973Met)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38581112G>CCA352139721SCN5Ac.3047C>G (p.Thr1016Arg)
c.2918C>G (p.Thr973Arg)
3g.38581112G=CA1358574363SCN5Ac.3047C= (p.Thr1016=)
c.2918C= (p.Thr973=)
3g.38581112G>TCA352139718SCN5Ac.3047C>A (p.Thr1016Lys)
c.2918C>A (p.Thr973Lys)
ClinVar dbSNP
3g.38581113T>ACA352139723SCN5Ac.3046A>T (p.Thr1016Ser)
c.2917A>T (p.Thr973Ser)
dbSNP
3g.38581113T>CCA352139725SCN5Ac.3046A>G (p.Thr1016Ala)
c.2917A>G (p.Thr973Ala)
3g.38581113T>GCA352139726SCN5Ac.3046A>C (p.Thr1016Pro)
c.2917A>C (p.Thr973Pro)
3g.38581116_38581117delCA2586972016SCN5Ac.3045_3046del (p.Glu1015AspfsTer14)
c.2916_2917del (p.Glu972AspfsTer14)
3g.38581114C>ACA352139728SCN5Ac.3045G>T (p.Glu1015Asp)
c.2916G>T (p.Glu972Asp)
3g.38581114C>GCA352139729SCN5Ac.3045G>C (p.Glu1015Asp)
c.2916G>C (p.Glu972Asp)
ClinVar dbSNP gnomAD v4
3g.38581114C>TCA433135501SCN5Ac.3045G>A (p.Glu1015=)
c.2916G>A (p.Glu972=)
3g.38581115T>ACA352139734SCN5Ac.3044A>T (p.Glu1015Val)
c.2915A>T (p.Glu972Val)
3g.38581115T>CCA352139732SCN5Ac.3044A>G (p.Glu1015Gly)
c.2915A>G (p.Glu972Gly)
3g.38581115T>GCA352139730SCN5Ac.3044A>C (p.Glu1015Ala)
c.2915A>C (p.Glu972Ala)
3g.38581116C>ACA352139737SCN5Ac.3043G>T (p.Glu1015Ter)
c.2914G>T (p.Glu972Ter)
dbSNP
3g.38581116C=CA1358574370SCN5Ac.3043G= (p.Glu1015=)
c.2914G= (p.Glu972=)
3g.38581116C>GCA352139739SCN5Ac.3043G>C (p.Glu1015Gln)
c.2914G>C (p.Glu972Gln)
3g.38581116C>TCA061210SCN5Ac.3043G>A (p.Glu1015Lys)
c.2914G>A (p.Glu972Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38581117T>ACA433135510SCN5Ac.3042A>T (p.Pro1014=)
c.2913A>T (p.Pro971=)
3g.38581117T>CCA433135512SCN5Ac.3042A>G (p.Pro1014=)
c.2913A>G (p.Pro971=)
dbSNP
3g.38581117T>GCA433135513SCN5Ac.3042A>C (p.Pro1014=)
c.2913A>C (p.Pro971=)
ClinVar dbSNP gnomAD v3 gnomAD v4
3g.38581117T=CA1358574374SCN5Ac.3042A= (p.Pro1014=)
c.2913A= (p.Pro971=)
3g.38581117_38581118delCA2573136279SCN5Ac.3041_3042del (p.Pro1014ArgfsTer15)
c.2912_2913del (p.Pro971ArgfsTer15)
ClinVar dbSNP
3g.38581118G>ACA352139740SCN5Ac.3041C>T (p.Pro1014Leu)
c.2912C>T (p.Pro971Leu)
3g.38581118G>CCA352139741SCN5Ac.3041C>G (p.Pro1014Arg)
c.2912C>G (p.Pro971Arg)
gnomAD v4
3g.38581118G>TCA352139742SCN5Ac.3041C>A (p.Pro1014Gln)
c.2912C>A (p.Pro971Gln)
3g.38581127_38581143dupCA1139657965SCN5Ac.3025_3041dup (p.Glu1015ThrfsTer?)
c.2896_2912dup (p.Glu972ThrfsTer?)
ClinVar dbSNP
3g.38581127_38581143delCA2665113032SCN5Ac.3025_3041del (p.Tyr1009ArgfsTer15)
c.2896_2912del (p.Tyr966ArgfsTer15)
ClinVar gnomAD v4
3g.38581119G>ACA352139743SCN5Ac.3040C>T (p.Pro1014Ser)
c.2911C>T (p.Pro971Ser)
ClinVar
3g.38581119G>CCA352139745SCN5Ac.3040C>G (p.Pro1014Ala)
c.2911C>G (p.Pro971Ala)
3g.38581119G>TCA352139744SCN5Ac.3040C>A (p.Pro1014Thr)
c.2911C>A (p.Pro971Thr)
ClinVar dbSNP COSMIC COSMIC COSMIC
3g.38581120G>ACA433135523SCN5Ac.3039C>T (p.Pro1013=)
c.2910C>T (p.Pro970=)
COSMIC COSMIC COSMIC
3g.38581120G>CCA433135525SCN5Ac.3039C>G (p.Pro1013=)
c.2910C>G (p.Pro970=)
3g.38581120G=CA1358574379SCN5Ac.3039C= (p.Pro1013=)
c.2910C= (p.Pro970=)
3g.38581120G>TCA061205SCN5Ac.3039C>A (p.Pro1013=)
c.2910C>A (p.Pro970=)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.38581121G>ACA352139748SCN5Ac.3038C>T (p.Pro1013Leu)
c.2909C>T (p.Pro970Leu)
3g.38581121G>CCA352139746SCN5Ac.3038C>G (p.Pro1013Arg)
c.2909C>G (p.Pro970Arg)
ClinVar dbSNP
3g.38581121G>TCA352139750SCN5Ac.3038C>A (p.Pro1013His)
c.2909C>A (p.Pro970His)
3g.38581122G>ACA352139752SCN5Ac.3037C>T (p.Pro1013Ser)
c.2908C>T (p.Pro970Ser)
gnomAD v4
3g.38581122G>CCA352139755SCN5Ac.3037C>G (p.Pro1013Ala)
c.2908C>G (p.Pro970Ala)
gnomAD v4
3g.38581122G>TCA352139754SCN5Ac.3037C>A (p.Pro1013Thr)
c.2908C>A (p.Pro970Thr)
3g.38581123T>ACA433135532SCN5Ac.3036A>T (p.Pro1012=)
c.2907A>T (p.Pro969=)
ClinVar
3g.38581123T>CCA433135534SCN5Ac.3036A>G (p.Pro1012=)
c.2907A>G (p.Pro969=)
3g.38581123T>GCA433135536SCN5Ac.3036A>C (p.Pro1012=)
c.2907A>C (p.Pro969=)
dbSNP gnomAD v3 gnomAD v4
3g.38581123T=CA1358574380SCN5Ac.3036A= (p.Pro1012=)
c.2907A= (p.Pro969=)
3g.38581124G>ACA352139758SCN5Ac.3035C>T (p.Pro1012Leu)
c.2906C>T (p.Pro969Leu)
3g.38581124G>CCA352139761SCN5Ac.3035C>G (p.Pro1012Arg)
c.2906C>G (p.Pro969Arg)
3g.38581124G>TCA352139760SCN5Ac.3035C>A (p.Pro1012Gln)
c.2906C>A (p.Pro969Gln)
gnomAD v4
3g.38581125G>ACA352139763SCN5Ac.3034C>T (p.Pro1012Ser)
c.2905C>T (p.Pro969Ser)
3g.38581125G>CCA352139765SCN5Ac.3034C>G (p.Pro1012Ala)
c.2905C>G (p.Pro969Ala)
3g.38581125G>TCA352139767SCN5Ac.3034C>A (p.Pro1012Thr)
c.2905C>A (p.Pro969Thr)
3g.38581126C>ACA433332490SCN5Ac.3033G>T (p.Pro1011=)
c.2904G>T (p.Pro968=)
ClinVar gnomAD v4
3g.38581126C=CA1358574387SCN5Ac.3033G= (p.Pro1011=)
c.2904G= (p.Pro968=)
3g.38581126C>GCA061201SCN5Ac.3033G>C (p.Pro1011=)
c.2904G>C (p.Pro968=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38581126C>TCA061197SCN5Ac.3033G>A (p.Pro1011=)
c.2904G>A (p.Pro968=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38581127G>ACA061192SCN5Ac.3032C>T (p.Pro1011Leu)
c.2903C>T (p.Pro968Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38581127G>CCA352139773SCN5Ac.3032C>G (p.Pro1011Arg)
c.2903C>G (p.Pro968Arg)
3g.38581127G=CA1358574391SCN5Ac.3032C= (p.Pro1011=)
c.2903C= (p.Pro968=)
3g.38581127G>TCA352139775SCN5Ac.3032C>A (p.Pro1011Gln)
c.2903C>A (p.Pro968Gln)
3g.38581128G>ACA061186SCN5Ac.3031C>T (p.Pro1011Ser)
c.2902C>T (p.Pro968Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38581128G>CCA352139779SCN5Ac.3031C>G (p.Pro1011Ala)
c.2902C>G (p.Pro968Ala)
dbSNP
3g.38581128G=CA1358574396SCN5Ac.3031C= (p.Pro1011=)
c.2902C= (p.Pro968=)
3g.38581128G>TCA352139781SCN5Ac.3031C>A (p.Pro1011Thr)
c.2902C>A (p.Pro968Thr)
3g.38581129G>ACA433332491SCN5Ac.3030C>T (p.Ser1010=)
c.2901C>T (p.Ser967=)
ClinVar dbSNP
3g.38581129G>CCA433332492SCN5Ac.3030C>G (p.Ser1010=)
c.2901C>G (p.Ser967=)
3g.38581129G>TCA433332493SCN5Ac.3030C>A (p.Ser1010=)
c.2901C>A (p.Ser967=)
gnomAD v4
3g.38581130G>ACA352139784SCN5Ac.3029C>T (p.Ser1010Phe)
c.2900C>T (p.Ser967Phe)
gnomAD v4
3g.38581130G>CCA352139787SCN5Ac.3029C>G (p.Ser1010Cys)
c.2900C>G (p.Ser967Cys)
3g.38581130G>TCA352139785SCN5Ac.3029C>A (p.Ser1010Tyr)
c.2900C>A (p.Ser967Tyr)
3g.38581131A>CCA352139789SCN5Ac.3028T>G (p.Ser1010Ala)
c.2899T>G (p.Ser967Ala)
3g.38581131A>GCA352139791SCN5Ac.3028T>C (p.Ser1010Pro)
c.2899T>C (p.Ser967Pro)
3g.38581131A>TCA352139793SCN5Ac.3028T>A (p.Ser1010Thr)
c.2899T>A (p.Ser967Thr)
gnomAD v4
3g.38581132G>ACA433332494SCN5Ac.3027C>T (p.Tyr1009=)
c.2898C>T (p.Tyr966=)
gnomAD v4
3g.38581132G>CCA352139795SCN5Ac.3027C>G (p.Tyr1009Ter)
c.2898C>G (p.Tyr966Ter)
3g.38581132G>TCA352139797SCN5Ac.3027C>A (p.Tyr1009Ter)
c.2898C>A (p.Tyr966Ter)
ClinVar dbSNP
3g.38581133T>ACA352139799SCN5Ac.3026A>T (p.Tyr1009Phe)
c.2897A>T (p.Tyr966Phe)
3g.38581133T>CCA352139801SCN5Ac.3026A>G (p.Tyr1009Cys)
c.2897A>G (p.Tyr966Cys)
3g.38581133T>GCA72926292SCN5Ac.3026A>C (p.Tyr1009Ser)
c.2897A>C (p.Tyr966Ser)
dbSNP gnomAD v3 gnomAD v4
3g.38581133T=CA1358574398SCN5Ac.3026A= (p.Tyr1009=)
c.2897A= (p.Tyr966=)
3g.38581134A=CA1358574400SCN5Ac.3025T= (p.Tyr1009=)
c.2896T= (p.Tyr966=)
3g.38581134A>CCA352139805SCN5Ac.3025T>G (p.Tyr1009Asp)
c.2896T>G (p.Tyr966Asp)
ClinVar
3g.38581134A>GCA352139807SCN5Ac.3025T>C (p.Tyr1009His)
c.2896T>C (p.Tyr966His)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.38581134A>TCA352139804SCN5Ac.3025T>A (p.Tyr1009Asn)
c.2896T>A (p.Tyr966Asn)
gnomAD v4
3g.38581135G>ACA433332495SCN5Ac.3024C>T (p.Pro1008=)
c.2895C>T (p.Pro965=)
gnomAD v4
3g.38581135G>CCA433332496SCN5Ac.3024C>G (p.Pro1008=)
c.2895C>G (p.Pro965=)
3g.38581135G>TCA433332497SCN5Ac.3024C>A (p.Pro1008=)
c.2895C>A (p.Pro965=)
3g.38581139dupCA2739279412SCN5Ac.3024dup (p.Tyr1009LeufsTer21)
c.2895dup (p.Tyr966LeufsTer21)
ClinVar
3g.38581139delCA433332498SCN5Ac.3024del (p.Tyr1009ThrfsTer?)
c.2895del (p.Tyr966ThrfsTer?)
COSMIC COSMIC COSMIC
3g.38581136G>ACA061176SCN5Ac.3023C>T (p.Pro1008Leu)
c.2894C>T (p.Pro965Leu)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.38581136G>CCA352139810SCN5Ac.3023C>G (p.Pro1008Arg)
c.2894C>G (p.Pro965Arg)
3g.38581136G=CA1358574402SCN5Ac.3023C= (p.Pro1008=)
c.2894C= (p.Pro965=)
3g.38581136G>TCA352139811SCN5Ac.3023C>A (p.Pro1008His)
c.2894C>A (p.Pro965His)
3g.38581136_38581149delinsGGGGTGGCAATGCACA1358574403SCN5Ac.3010_3023delinsTGCATTGCCACCCC (p.Cys1004=)
c.2881_2894delinsTGCATTGCCACCCC (p.Cys961=)
3g.38581137G>ACA016755SCN5Ac.3022C>T (p.Pro1008Ser)
c.2893C>T (p.Pro965Ser)
ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC COSMIC
3g.38581137G>CCA352139815SCN5Ac.3022C>G (p.Pro1008Ala)
c.2893C>G (p.Pro965Ala)
ClinVar gnomAD v4
3g.38581137G=CA1358574407SCN5Ac.3022C= (p.Pro1008=)
c.2893C= (p.Pro965=)
3g.38581137G>TCA352139817SCN5Ac.3022C>A (p.Pro1008Thr)
c.2893C>A (p.Pro965Thr)
dbSNP gnomAD v4
3g.38581138_38581150delCA16611470SCN5Ac.3010_3022del (p.Cys1004ProfsTer?)
c.2881_2893del (p.Cys961ProfsTer?)
ClinVar dbSNP
3g.38581138G>ACA433332499SCN5Ac.3021C>T (p.Thr1007=)
c.2892C>T (p.Thr964=)
3g.38581138G>CCA433332500SCN5Ac.3021C>G (p.Thr1007=)
c.2892C>G (p.Thr964=)
3g.38581138G>TCA433332501SCN5Ac.3021C>A (p.Thr1007=)
c.2892C>A (p.Thr964=)
3g.38581139G>ACA061168SCN5Ac.3020C>T (p.Thr1007Ile)
c.2891C>T (p.Thr964Ile)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38581139G>CCA352139820SCN5Ac.3020C>G (p.Thr1007Ser)
c.2891C>G (p.Thr964Ser)
3g.38581139G=CA1358574409SCN5Ac.3020C= (p.Thr1007=)
c.2891C= (p.Thr964=)
3g.38581139G>TCA72926298SCN5Ac.3020C>A (p.Thr1007Asn)
c.2891C>A (p.Thr964Asn)
ClinVar dbSNP gnomAD v2
3g.38581140delCA2580617587SCN5Ac.3019del (p.Thr1007ProfsTer?)
c.2890del (p.Thr964ProfsTer?)
3g.38581140T>ACA352139824SCN5Ac.3019A>T (p.Thr1007Ser)
c.2890A>T (p.Thr964Ser)
3g.38581140T>CCA352139826SCN5Ac.3019A>G (p.Thr1007Ala)
c.2890A>G (p.Thr964Ala)
3g.38581140T>GCA352139828SCN5Ac.3019A>C (p.Thr1007Pro)
c.2890A>C (p.Thr964Pro)
dbSNP
3g.38581140T=CA1358574411SCN5Ac.3019A= (p.Thr1007=)
c.2890A= (p.Thr964=)
3g.38581141G>ACA433332504SCN5Ac.3018C>T (p.Ala1006=)
c.2889C>T (p.Ala963=)
3g.38581141G>CCA433332503SCN5Ac.3018C>G (p.Ala1006=)
c.2889C>G (p.Ala963=)
3g.38581141G>TCA433332502SCN5Ac.3018C>A (p.Ala1006=)
c.2889C>A (p.Ala963=)
3g.38581142G>ACA352139835SCN5Ac.3017C>T (p.Ala1006Val)
c.2888C>T (p.Ala963Val)
3g.38581142G>CCA352139831SCN5Ac.3017C>G (p.Ala1006Gly)
c.2888C>G (p.Ala963Gly)
3g.38581142G>TCA352139832SCN5Ac.3017C>A (p.Ala1006Asp)
c.2888C>A (p.Ala963Asp)
ClinVar dbSNP gnomAD v4
3g.38581143C>ACA061161SCN5Ac.3016G>T (p.Ala1006Ser)
c.2887G>T (p.Ala963Ser)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38581143C=CA1358574413SCN5Ac.3016G= (p.Ala1006=)
c.2887G= (p.Ala963=)
3g.38581143C>GCA352139842SCN5Ac.3016G>C (p.Ala1006Pro)
c.2887G>C (p.Ala963Pro)
3g.38581143C>TCA352139844SCN5Ac.3016G>A (p.Ala1006Thr)
c.2887G>A (p.Ala963Thr)
gnomAD v4
3g.38581144A>CCA352139847SCN5Ac.3015T>G (p.Ile1005Met)
c.2886T>G (p.Ile962Met)
3g.38581144A>GCA433332505SCN5Ac.3015T>C (p.Ile1005=)
c.2886T>C (p.Ile962=)
gnomAD v4
3g.38581144A>TCA433332506SCN5Ac.3015T>A (p.Ile1005=)
c.2886T>A (p.Ile962=)
3g.38581145A=CA1358574415SCN5Ac.3014T= (p.Ile1005=)
c.2885T= (p.Ile962=)
3g.38581145A>CCA352139849SCN5Ac.3014T>G (p.Ile1005Ser)
c.2885T>G (p.Ile962Ser)
3g.38581145A>GCA061157SCN5Ac.3014T>C (p.Ile1005Thr)
c.2885T>C (p.Ile962Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.38581145A>TCA352139852SCN5Ac.3014T>A (p.Ile1005Asn)
c.2885T>A (p.Ile962Asn)
gnomAD v4
3g.38581146T>ACA352139854SCN5Ac.3013A>T (p.Ile1005Phe)
c.2884A>T (p.Ile962Phe)
ClinVar dbSNP
3g.38581146T>CCA352139856SCN5Ac.3013A>G (p.Ile1005Val)
c.2884A>G (p.Ile962Val)
ClinVar dbSNP gnomAD v2 gnomAD v4
3g.38581146T>GCA352139857SCN5Ac.3013A>C (p.Ile1005Leu)
c.2884A>C (p.Ile962Leu)
3g.38581146T=CA1358574417SCN5Ac.3013A= (p.Ile1005=)
c.2884A= (p.Ile962=)
3g.38581147G>ACA433332507SCN5Ac.3012C>T (p.Cys1004=)
c.2883C>T (p.Cys961=)
ClinVar dbSNP gnomAD v4
3g.38581147G>CCA352139859SCN5Ac.3012C>G (p.Cys1004Trp)
c.2883C>G (p.Cys961Trp)
3g.38581147G=CA1358574419SCN5Ac.3012C= (p.Cys1004=)
c.2883C= (p.Cys961=)
3g.38581147G>TCA352139860SCN5Ac.3012C>A (p.Cys1004Ter)
c.2883C>A (p.Cys961Ter)
3g.38581155_38581162dupCA2580614201SCN5Ac.3005_3012dup (p.Ile1005ProfsTer?)
c.2876_2883dup (p.Ile962ProfsTer?)
ClinVar gnomAD v4
3g.38581155_38581162delCA2586972017SCN5Ac.3005_3012del (p.Pro1002HisfsTer25)
c.2876_2883del (p.Pro959HisfsTer25)
3g.38581148C>ACA352139864SCN5Ac.3011G>T (p.Cys1004Phe)
c.2882G>T (p.Cys961Phe)
3g.38581148C>GCA352139866SCN5Ac.3011G>C (p.Cys1004Ser)
c.2882G>C (p.Cys961Ser)
3g.38581148C>TCA352139861SCN5Ac.3011G>A (p.Cys1004Tyr)
c.2882G>A (p.Cys961Tyr)
3g.38581149A=CA1358574423SCN5Ac.3010T= (p.Cys1004=)
c.2881T= (p.Cys961=)
3g.38581149A>CCA352139870SCN5Ac.3010T>G (p.Cys1004Gly)
c.2881T>G (p.Cys961Gly)
dbSNP gnomAD v3 gnomAD v4
3g.38581149A>GCA016748SCN5Ac.3010T>C (p.Cys1004Arg)
c.2881T>C (p.Cys961Arg)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38581149A>TCA352139868SCN5Ac.3010T>A (p.Cys1004Ser)
c.2881T>A (p.Cys961Ser)
3g.38581150G>ACA433332508SCN5Ac.3009C>T (p.Ser1003=)
c.2880C>T (p.Ser960=)
COSMIC COSMIC COSMIC
3g.38581150G>CCA352139872SCN5Ac.3009C>G (p.Ser1003Arg)
c.2880C>G (p.Ser960Arg)
3g.38581150G>TCA352139874SCN5Ac.3009C>A (p.Ser1003Arg)
c.2880C>A (p.Ser960Arg)
3g.38581151C>ACA352139876SCN5Ac.3008G>T (p.Ser1003Ile)
c.2879G>T (p.Ser960Ile)
3g.38581151C>GCA352139878SCN5Ac.3008G>C (p.Ser1003Thr)
c.2879G>C (p.Ser960Thr)
3g.38581151C>TCA352139880SCN5Ac.3008G>A (p.Ser1003Asn)
c.2879G>A (p.Ser960Asn)
3g.38581152T>ACA352139882SCN5Ac.3007A>T (p.Ser1003Cys)
c.2878A>T (p.Ser960Cys)
3g.38581152T>CCA352139884SCN5Ac.3007A>G (p.Ser1003Gly)
c.2878A>G (p.Ser960Gly)
ClinVar
3g.38581152T>GCA352139886SCN5Ac.3007A>C (p.Ser1003Arg)
c.2878A>C (p.Ser960Arg)
3g.38581153G>ACA433332509SCN5Ac.3006C>T (p.Pro1002=)
c.2877C>T (p.Pro959=)
3g.38581153G>CCA433332510SCN5Ac.3006C>G (p.Pro1002=)
c.2877C>G (p.Pro959=)
ClinVar dbSNP gnomAD v3 gnomAD v4
3g.38581153G=CA1358574425SCN5Ac.3006C= (p.Pro1002=)
c.2877C= (p.Pro959=)
3g.38581153G>TCA433332511SCN5Ac.3006C>A (p.Pro1002=)
c.2877C>A (p.Pro959=)
3g.38581155delCA2739279413SCN5Ac.3006del (p.Ser1003AlafsTer?)
c.2877del (p.Ser960AlafsTer?)
ClinVar
3g.38581154G>ACA352139888SCN5Ac.3005C>T (p.Pro1002Leu)
c.2876C>T (p.Pro959Leu)
dbSNP gnomAD v4
3g.38581154G>CCA352139890SCN5Ac.3005C>G (p.Pro1002Arg)
c.2876C>G (p.Pro959Arg)
3g.38581154G=CA1358574427SCN5Ac.3005C= (p.Pro1002=)
c.2876C= (p.Pro959=)
3g.38581154G>TCA352139892SCN5Ac.3005C>A (p.Pro1002His)
c.2876C>A (p.Pro959His)
3g.38581155G>ACA061148SCN5Ac.3004C>T (p.Pro1002Ser)
c.2875C>T (p.Pro959Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.38581155G>CCA352139895SCN5Ac.3004C>G (p.Pro1002Ala)
c.2875C>G (p.Pro959Ala)
3g.38581155G=CA1358574428SCN5Ac.3004C= (p.Pro1002=)
c.2875C= (p.Pro959=)
3g.38581155G>TCA352139893SCN5Ac.3004C>A (p.Pro1002Thr)
c.2875C>A (p.Pro959Thr)
3g.38581156C>ACA433332512SCN5Ac.3003G>T (p.Leu1001=)
c.2874G>T (p.Leu958=)
dbSNP gnomAD v3 gnomAD v4
3g.38581156C=CA1358574429SCN5Ac.3003G= (p.Leu1001=)
c.2874G= (p.Leu958=)
3g.38581156C>GCA061143SCN5Ac.3003G>C (p.Leu1001=)
c.2874G>C (p.Leu958=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38581156C>TCA433332513SCN5Ac.3003G>A (p.Leu1001=)
c.2874G>A (p.Leu958=)
3g.38581157A>CCA352139898SCN5Ac.3002T>G (p.Leu1001Arg)
c.2873T>G (p.Leu958Arg)
3g.38581157A>GCA352139900SCN5Ac.3002T>C (p.Leu1001Pro)
c.2873T>C (p.Leu958Pro)
3g.38581157A>TCA352139901SCN5Ac.3002T>A (p.Leu1001Gln)
c.2873T>A (p.Leu958Gln)
3g.38581157_38581160delinsAGCTCA1358574430SCN5Ac.2999_3002delinsAGCT (p.Gln1000=)
c.2870_2873delinsAGCT (p.Gln957=)
3g.38581158G>ACA433332514SCN5Ac.3001C>T (p.Leu1001=)
c.2872C>T (p.Leu958=)
gnomAD v4
3g.38581158G>CCA352139903SCN5Ac.3001C>G (p.Leu1001Val)
c.2872C>G (p.Leu958Val)
ClinVar gnomAD v4
3g.38581158G>TCA352139905SCN5Ac.3001C>A (p.Leu1001Met)
c.2872C>A (p.Leu958Met)
3g.38581159_38581161delCA061128SCN5Ac.2999_3001del (p.Gln1000del)
c.2870_2872del (p.Gln957del)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38581159C>ACA352139907SCN5Ac.3000G>T (p.Gln1000His)
c.2871G>T (p.Gln957His)
3g.38581159C=CA1358574431SCN5Ac.3000G= (p.Gln1000=)
c.2871G= (p.Gln957=)
3g.38581159C>GCA352139908SCN5Ac.3000G>C (p.Gln1000His)
c.2871G>C (p.Gln957His)
3g.38581159C>TCA72926311SCN5Ac.3000G>A (p.Gln1000=)
c.2871G>A (p.Gln957=)
ClinVar dbSNP gnomAD v4
3g.38581160T>ACA061132SCN5Ac.2999A>T (p.Gln1000Leu)
c.2870A>T (p.Gln957Leu)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.38581160T>CCA352139913SCN5Ac.2999A>G (p.Gln1000Arg)
c.2870A>G (p.Gln957Arg)
3g.38581160T>GCA352139911SCN5Ac.2999A>C (p.Gln1000Pro)
c.2870A>C (p.Gln957Pro)
3g.38581160T=CA1358574433SCN5Ac.2999A= (p.Gln1000=)
c.2870A= (p.Gln957=)
3g.38581161G>ACA352139914SCN5Ac.2998C>T (p.Gln1000Ter)
c.2869C>T (p.Gln957Ter)
ClinVar
3g.38581161G>CCA352139916SCN5Ac.2998C>G (p.Gln1000Glu)
c.2869C>G (p.Gln957Glu)
3g.38581161G>TCA352139918SCN5Ac.2998C>A (p.Gln1000Lys)
c.2869C>A (p.Gln957Lys)
3g.38581162G>ACA433332516SCN5Ac.2997C>T (p.Gly999=)
c.2868C>T (p.Gly956=)
3g.38581162G>CCA433332517SCN5Ac.2997C>G (p.Gly999=)
c.2868C>G (p.Gly956=)
3g.38581162G>TCA433332515SCN5Ac.2997C>A (p.Gly999=)
c.2868C>A (p.Gly956=)
gnomAD v4
3g.38581163C>ACA352139920SCN5Ac.2996G>T (p.Gly999Val)
c.2867G>T (p.Gly956Val)
3g.38581163C=CA1358574434SCN5Ac.2996G= (p.Gly999=)
c.2867G= (p.Gly956=)
3g.38581163C>GCA352139922SCN5Ac.2996G>C (p.Gly999Ala)
c.2867G>C (p.Gly956Ala)
3g.38581163C>TCA352139923SCN5Ac.2996G>A (p.Gly999Asp)
c.2867G>A (p.Gly956Asp)
ClinVar dbSNP gnomAD v2 gnomAD v4
3g.38581164C>ACA352139930SCN5Ac.2995G>T (p.Gly999Cys)
c.2866G>T (p.Gly956Cys)
COSMIC COSMIC COSMIC
3g.38581164C>GCA352139926SCN5Ac.2995G>C (p.Gly999Arg)
c.2866G>C (p.Gly956Arg)
3g.38581164C>TCA352139927SCN5Ac.2995G>A (p.Gly999Ser)
c.2866G>A (p.Gly956Ser)
3g.38581165C>ACA352139932SCN5Ac.2994G>T (p.Gln998His)
c.2865G>T (p.Gln955His)
COSMIC COSMIC COSMIC
3g.38581165C=CA1358574436SCN5Ac.2994G= (p.Gln998=)
c.2865G= (p.Gln955=)
3g.38581165C>GCA352139934SCN5Ac.2994G>C (p.Gln998His)
c.2865G>C (p.Gln955His)
3g.38581165C>TCA433332518SCN5Ac.2994G>A (p.Gln998=)
c.2865G>A (p.Gln955=)
ClinVar dbSNP gnomAD v4
3g.38581166T>ACA352139936SCN5Ac.2993A>T (p.Gln998Leu)
c.2864A>T (p.Gln955Leu)
3g.38581166T>CCA016741SCN5Ac.2993A>G (p.Gln998Arg)
c.2864A>G (p.Gln955Arg)
ClinVar dbSNP
3g.38581166T>GCA352139939SCN5Ac.2993A>C (p.Gln998Pro)
c.2864A>C (p.Gln955Pro)
dbSNP
3g.38581166T=CA1358574438SCN5Ac.2993A= (p.Gln998=)
c.2864A= (p.Gln955=)
3g.38581167G>ACA352139941SCN5Ac.2992C>T (p.Gln998Ter)
c.2863C>T (p.Gln955Ter)
3g.38581167G>CCA352139945SCN5Ac.2992C>G (p.Gln998Glu)
c.2863C>G (p.Gln955Glu)
3g.38581167G>TCA352139943SCN5Ac.2992C>A (p.Gln998Lys)
c.2863C>A (p.Gln955Lys)
3g.38581168G>ACA433332519SCN5Ac.2991C>T (p.Ala997=)
c.2862C>T (p.Ala954=)
3g.38581168G>CCA433332520SCN5Ac.2991C>G (p.Ala997=)
c.2862C>G (p.Ala954=)
3g.38581168G>TCA433332521SCN5Ac.2991C>A (p.Ala997=)
c.2862C>A (p.Ala954=)
3g.38581169G>ACA352139948SCN5Ac.2990C>T (p.Ala997Val)
c.2861C>T (p.Ala954Val)
3g.38581169G>CCA352139949SCN5Ac.2990C>G (p.Ala997Gly)
c.2861C>G (p.Ala954Gly)
3g.38581169G=CA1358574440SCN5Ac.2990C= (p.Ala997=)
c.2861C= (p.Ala954=)
3g.38581169G>TCA016729SCN5Ac.2990C>A (p.Ala997Asp)
c.2861C>A (p.Ala954Asp)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38581170C>ACA016718SCN5Ac.2989G>T (p.Ala997Ser)
c.2860G>T (p.Ala954Ser)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.38581170C=CA1358574442SCN5Ac.2989G= (p.Ala997=)
c.2860G= (p.Ala954=)
3g.38581170C>GCA352139953SCN5Ac.2989G>C (p.Ala997Pro)
c.2860G>C (p.Ala954Pro)
3g.38581170C>TCA016710SCN5Ac.2989G>A (p.Ala997Thr)
c.2860G>A (p.Ala954Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38581171G>ACA061120SCN5Ac.2988C>T (p.Ala996=)
c.2859C>T (p.Ala953=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38581171G>CCA433332522SCN5Ac.2988C>G (p.Ala996=)
c.2859C>G (p.Ala953=)
3g.38581171G=CA1358574443SCN5Ac.2988C= (p.Ala996=)
c.2859C= (p.Ala953=)
3g.38581171G>TCA433332523SCN5Ac.2988C>A (p.Ala996=)
c.2859C>A (p.Ala953=)
3g.38581172G>ACA352139957SCN5Ac.2987C>T (p.Ala996Val)
c.2858C>T (p.Ala953Val)
gnomAD v4
3g.38581172G>CCA352139958SCN5Ac.2987C>G (p.Ala996Gly)
c.2858C>G (p.Ala953Gly)
3g.38581172G=CA1358574446SCN5Ac.2987C= (p.Ala996=)
c.2858C= (p.Ala953=)
3g.38581172G>TCA352139961SCN5Ac.2987C>A (p.Ala996Asp)
c.2858C>A (p.Ala953Asp)
ClinVar dbSNP gnomAD v2 gnomAD v4
3g.38581173C>ACA352139963SCN5Ac.2986G>T (p.Ala996Ser)
c.2857G>T (p.Ala953Ser)
3g.38581173C=CA1358574447SCN5Ac.2986G= (p.Ala996=)
c.2857G= (p.Ala953=)
3g.38581173C>GCA352139965SCN5Ac.2986G>C (p.Ala996Pro)
c.2857G>C (p.Ala953Pro)
3g.38581173C>TCA352139967SCN5Ac.2986G>A (p.Ala996Thr)
c.2857G>A (p.Ala953Thr)
dbSNP gnomAD v2 gnomAD v4
3g.38581174A>CCA433332524SCN5Ac.2985T>G (p.Leu995=)
c.2856T>G (p.Leu952=)
3g.38581174A>GCA433332525SCN5Ac.2985T>C (p.Leu995=)
c.2856T>C (p.Leu952=)
3g.38581174A>TCA433332526SCN5Ac.2985T>A (p.Leu995=)
c.2856T>A (p.Leu952=)
3g.38581175A>CCA352139971SCN5Ac.2984T>G (p.Leu995Arg)
c.2855T>G (p.Leu952Arg)
3g.38581175A>GCA352139974SCN5Ac.2984T>C (p.Leu995Pro)
c.2855T>C (p.Leu952Pro)
3g.38581175A>TCA352139970SCN5Ac.2984T>A (p.Leu995His)
c.2855T>A (p.Leu952His)
3g.38581176G>ACA061116SCN5Ac.2983C>T (p.Leu995Phe)
c.2854C>T (p.Leu952Phe)
dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC COSMIC
3g.38581176G>CCA352139976SCN5Ac.2983C>G (p.Leu995Val)
c.2854C>G (p.Leu952Val)
3g.38581176G=CA1358574449SCN5Ac.2983C= (p.Leu995=)
c.2854C= (p.Leu952=)
3g.38581176G>TCA352139979SCN5Ac.2983C>A (p.Leu995Ile)
c.2854C>A (p.Leu952Ile)
3g.38581177G>ACA433332527SCN5Ac.2982C>T (p.Ala994=)
c.2853C>T (p.Ala951=)
gnomAD v4 COSMIC COSMIC COSMIC
3g.38581177G>CCA433332528SCN5Ac.2982C>G (p.Ala994=)
c.2853C>G (p.Ala951=)
3g.38581177G>TCA433332529SCN5Ac.2982C>A (p.Ala994=)
c.2853C>A (p.Ala951=)
ClinVar gnomAD v4
3g.38581178G>ACA352139981SCN5Ac.2981C>T (p.Ala994Val)
c.2852C>T (p.Ala951Val)
ClinVar dbSNP gnomAD v2 gnomAD v4
3g.38581178G>CCA352139983SCN5Ac.2981C>G (p.Ala994Gly)
c.2852C>G (p.Ala951Gly)
3g.38581178G=CA1358574451SCN5Ac.2981C= (p.Ala994=)
c.2852C= (p.Ala951=)
3g.38581178G>TCA352139985SCN5Ac.2981C>A (p.Ala994Asp)
c.2852C>A (p.Ala951Asp)
3g.38581179C>ACA352139988SCN5Ac.2980G>T (p.Ala994Ser)
c.2851G>T (p.Ala951Ser)
3g.38581179C=CA1358574452SCN5Ac.2980G= (p.Ala994=)
c.2851G= (p.Ala951=)
3g.38581179C>GCA352139990SCN5Ac.2980G>C (p.Ala994Pro)
c.2851G>C (p.Ala951Pro)
3g.38581179C>TCA352139991SCN5Ac.2980G>A (p.Ala994Thr)
c.2851G>A (p.Ala951Thr)
ClinVar dbSNP gnomAD v2 gnomAD v4
3g.38581180T>ACA433332530SCN5Ac.2979A>T (p.Ala993=)
c.2850A>T (p.Ala950=)
3g.38581180T>CCA433332531SCN5Ac.2979A>G (p.Ala993=)
c.2850A>G (p.Ala950=)
3g.38581180T>GCA433332532SCN5Ac.2979A>C (p.Ala993=)
c.2850A>C (p.Ala950=)
3g.38581181G>ACA352139994SCN5Ac.2978C>T (p.Ala993Val)
c.2849C>T (p.Ala950Val)
3g.38581181G>CCA352139996SCN5Ac.2978C>G (p.Ala993Gly)
c.2849C>G (p.Ala950Gly)
3g.38581181G>TCA352139997SCN5Ac.2978C>A (p.Ala993Glu)
c.2849C>A (p.Ala950Glu)
gnomAD v4
3g.38581182C>ACA352139999SCN5Ac.2977G>T (p.Ala993Ser)
c.2848G>T (p.Ala950Ser)
ClinVar dbSNP gnomAD v2 gnomAD v4
3g.38581182C=CA1358574453SCN5Ac.2977G= (p.Ala993=)
c.2848G= (p.Ala950=)
3g.38581182C>GCA352140001SCN5Ac.2977G>C (p.Ala993Pro)
c.2848G>C (p.Ala950Pro)
ClinVar
3g.38581182C>TCA061107SCN5Ac.2977G>A (p.Ala993Thr)
c.2848G>A (p.Ala950Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38581183G>ACA016703SCN5Ac.2976C>T (p.Pro992=)
c.2847C>T (p.Pro949=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38581183G>CCA433332534SCN5Ac.2976C>G (p.Pro992=)
c.2847C>G (p.Pro949=)
3g.38581183G=CA1358574456SCN5Ac.2976C= (p.Pro992=)
c.2847C= (p.Pro949=)
3g.38581183G>TCA433332533SCN5Ac.2976C>A (p.Pro992=)
c.2847C>A (p.Pro949=)
3g.38581185dupCA2665113033SCN5Ac.2976dup (p.Ala993ArgfsTer?)
c.2847dup (p.Ala950ArgfsTer?)
gnomAD v4
3g.38581184G>ACA72926345SCN5Ac.2975C>T (p.Pro992Leu)
c.2846C>T (p.Pro949Leu)
dbSNP gnomAD v4
3g.38581184G>CCA352140006SCN5Ac.2975C>G (p.Pro992Arg)
c.2846C>G (p.Pro949Arg)
3g.38581184G=CA1358574458SCN5Ac.2975C= (p.Pro992=)
c.2846C= (p.Pro949=)
3g.38581184G>TCA352140010SCN5Ac.2975C>A (p.Pro992His)
c.2846C>A (p.Pro949His)
gnomAD v4
3g.38581185G>ACA352140013SCN5Ac.2974C>T (p.Pro992Ser)
c.2845C>T (p.Pro949Ser)
3g.38581185G>CCA352140015SCN5Ac.2974C>G (p.Pro992Ala)
c.2845C>G (p.Pro949Ala)
3g.38581185G>TCA352140017SCN5Ac.2974C>A (p.Pro992Thr)
c.2845C>A (p.Pro949Thr)
ClinVar dbSNP
3g.38581186C>ACA352140019SCN5Ac.2973G>T (p.Lys991Asn)
c.2844G>T (p.Lys948Asn)
dbSNP
3g.38581186C=CA1358574460SCN5Ac.2973G= (p.Lys991=)
c.2844G= (p.Lys948=)
3g.38581186C>GCA352140020SCN5Ac.2973G>C (p.Lys991Asn)
c.2844G>C (p.Lys948Asn)
3g.38581186C>TCA16617950SCN5Ac.2973G>A (p.Lys991=)
c.2844G>A (p.Lys948=)
ClinVar dbSNP gnomAD v4
3g.38581187T>ACA352140022SCN5Ac.2972A>T (p.Lys991Met)
c.2843A>T (p.Lys948Met)
3g.38581187T>CCA352140023SCN5Ac.2972A>G (p.Lys991Arg)
c.2843A>G (p.Lys948Arg)
3g.38581187T>GCA352140025SCN5Ac.2972A>C (p.Lys991Thr)
c.2843A>C (p.Lys948Thr)
dbSNP gnomAD v2 gnomAD v4
3g.38581187T=CA1358574462SCN5Ac.2972A= (p.Lys991=)
c.2843A= (p.Lys948=)
3g.38581187_38581188delCA2825001218SCN5Ac.2971_2972del (p.Lys991AlafsTer?)
c.2842_2843del (p.Lys948AlafsTer?)
ClinVar
3g.38581188T>ACA352140028SCN5Ac.2971A>T (p.Lys991Ter)
c.2842A>T (p.Lys948Ter)
dbSNP
3g.38581188T>CCA061101SCN5Ac.2971A>G (p.Lys991Glu)
c.2842A>G (p.Lys948Glu)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.38581188T>GCA352140030SCN5Ac.2971A>C (p.Lys991Gln)
c.2842A>C (p.Lys948Gln)
3g.38581188T=CA1358574464SCN5Ac.2971A= (p.Lys991=)
c.2842A= (p.Lys948=)
3g.38581189C>ACA352140035SCN5Ac.2970G>T (p.Gln990His)
c.2841G>T (p.Gln947His)
3g.38581189C=CA1358574465SCN5Ac.2970G= (p.Gln990=)
c.2841G= (p.Gln947=)
3g.38581189C>GCA352140033SCN5Ac.2970G>C (p.Gln990His)
c.2841G>C (p.Gln947His)
3g.38581189C>TCA061096SCN5Ac.2970G>A (p.Gln990=)
c.2841G>A (p.Gln947=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4

Number of alleles fetched