Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.38576686C>ACA352138372SCN5Ac.3483G>T (p.Lys1161Asn)
c.3486G>T (p.Lys1162Asn)
c.3324G>T (p.Lys1108Asn)
c.3357G>T (p.Lys1119Asn)
3g.38576686C>GCA352138371SCN5Ac.3483G>C (p.Lys1161Asn)
c.3486G>C (p.Lys1162Asn)
c.3324G>C (p.Lys1108Asn)
c.3357G>C (p.Lys1119Asn)
3g.38576686C>TCA433134120SCN5Ac.3483G>A (p.Lys1161=)
c.3486G>A (p.Lys1162=)
c.3324G>A (p.Lys1108=)
c.3357G>A (p.Lys1119=)
3g.38576687T>ACA352138373SCN5Ac.3482A>T (p.Lys1161Met)
c.3485A>T (p.Lys1162Met)
c.3323A>T (p.Lys1108Met)
c.3356A>T (p.Lys1119Met)
3g.38576687T>CCA352138374SCN5Ac.3482A>G (p.Lys1161Arg)
c.3485A>G (p.Lys1162Arg)
c.3323A>G (p.Lys1108Arg)
c.3356A>G (p.Lys1119Arg)
3g.38576687T>GCA352138375SCN5Ac.3482A>C (p.Lys1161Thr)
c.3485A>C (p.Lys1162Thr)
c.3323A>C (p.Lys1108Thr)
c.3356A>C (p.Lys1119Thr)
3g.38576688T>ACA352138376SCN5Ac.3481A>T (p.Lys1161Ter)
c.3484A>T (p.Lys1162Ter)
c.3322A>T (p.Lys1108Ter)
c.3355A>T (p.Lys1119Ter)
 dbSNP
3g.38576688T>CCA352138377SCN5Ac.3481A>G (p.Lys1161Glu)
c.3484A>G (p.Lys1162Glu)
c.3322A>G (p.Lys1108Glu)
c.3355A>G (p.Lys1119Glu)
3g.38576688T>GCA352138378SCN5Ac.3481A>C (p.Lys1161Gln)
c.3484A>C (p.Lys1162Gln)
c.3322A>C (p.Lys1108Gln)
c.3355A>C (p.Lys1119Gln)
3g.38576688T=CA1358573157SCN5Ac.3481A= (p.Lys1161=)
c.3484A= (p.Lys1162=)
c.3322A= (p.Lys1108=)
c.3355A= (p.Lys1119=)
3g.38576689G>ACA433134124SCN5Ac.3480C>T (p.Val1160=)
c.3483C>T (p.Val1161=)
c.3321C>T (p.Val1107=)
c.3354C>T (p.Val1118=)
 dbSNP gnomAD v2 gnomAD v4
3g.38576689G>CCA433134125SCN5Ac.3480C>G (p.Val1160=)
c.3483C>G (p.Val1161=)
c.3321C>G (p.Val1107=)
c.3354C>G (p.Val1118=)
 COSMIC COSMIC COSMIC
3g.38576689G=CA1358573158SCN5Ac.3480C= (p.Val1160=)
c.3483C= (p.Val1161=)
c.3321C= (p.Val1107=)
c.3354C= (p.Val1118=)
3g.38576689G>TCA433134126SCN5Ac.3480C>A (p.Val1160=)
c.3483C>A (p.Val1161=)
c.3321C>A (p.Val1107=)
c.3354C>A (p.Val1118=)
 gnomAD v4
3g.38576690A>CCA352138381SCN5Ac.3479T>G (p.Val1160Gly)
c.3482T>G (p.Val1161Gly)
c.3320T>G (p.Val1107Gly)
c.3353T>G (p.Val1118Gly)
3g.38576690A>GCA352138379SCN5Ac.3479T>C (p.Val1160Ala)
c.3482T>C (p.Val1161Ala)
c.3320T>C (p.Val1107Ala)
c.3353T>C (p.Val1118Ala)
3g.38576690A>TCA352138380SCN5Ac.3479T>A (p.Val1160Asp)
c.3482T>A (p.Val1161Asp)
c.3320T>A (p.Val1107Asp)
c.3353T>A (p.Val1118Asp)
3g.38576691C>ACA352138382SCN5Ac.3478G>T (p.Val1160Phe)
c.3481G>T (p.Val1161Phe)
c.3319G>T (p.Val1107Phe)
c.3352G>T (p.Val1118Phe)
3g.38576691C>GCA352138383SCN5Ac.3478G>C (p.Val1160Leu)
c.3481G>C (p.Val1161Leu)
c.3319G>C (p.Val1107Leu)
c.3352G>C (p.Val1118Leu)
3g.38576691C>TCA352138384SCN5Ac.3478G>A (p.Val1160Ile)
c.3481G>A (p.Val1161Ile)
c.3319G>A (p.Val1107Ile)
c.3352G>A (p.Val1118Ile)
3g.38576692delCA2586972095SCN5Ac.3477del (p.Asp1159GlufsTer?)
c.3480del (p.Asp1160GlufsTer?)
c.3318del (p.Asp1106GlufsTer?)
c.3351del (p.Asp1117GlufsTer?)
3g.38576692A>CCA352138385SCN5Ac.3477T>G (p.Asp1159Glu)
c.3480T>G (p.Asp1160Glu)
c.3318T>G (p.Asp1106Glu)
c.3351T>G (p.Asp1117Glu)
3g.38576692A>GCA433134130SCN5Ac.3477T>C (p.Asp1159=)
c.3480T>C (p.Asp1160=)
c.3318T>C (p.Asp1106=)
c.3351T>C (p.Asp1117=)
3g.38576692A>TCA352138386SCN5Ac.3477T>A (p.Asp1159Glu)
c.3480T>A (p.Asp1160Glu)
c.3318T>A (p.Asp1106Glu)
c.3351T>A (p.Asp1117Glu)
3g.38576693T>ACA352138387SCN5Ac.3476A>T (p.Asp1159Val)
c.3479A>T (p.Asp1160Val)
c.3317A>T (p.Asp1106Val)
c.3350A>T (p.Asp1117Val)
3g.38576693T>CCA352138388SCN5Ac.3476A>G (p.Asp1159Gly)
c.3479A>G (p.Asp1160Gly)
c.3317A>G (p.Asp1106Gly)
c.3350A>G (p.Asp1117Gly)
 dbSNP
3g.38576693T>GCA352138389SCN5Ac.3476A>C (p.Asp1159Ala)
c.3479A>C (p.Asp1160Ala)
c.3317A>C (p.Asp1106Ala)
c.3350A>C (p.Asp1117Ala)
3g.38576693T=CA1358573159SCN5Ac.3476A= (p.Asp1159=)
c.3479A= (p.Asp1160=)
c.3317A= (p.Asp1106=)
c.3350A= (p.Asp1117=)
3g.38576694C>ACA352138390SCN5Ac.3475G>T (p.Asp1159Tyr)
c.3478G>T (p.Asp1160Tyr)
c.3316G>T (p.Asp1106Tyr)
c.3349G>T (p.Asp1117Tyr)
3g.38576694C>GCA352138391SCN5Ac.3475G>C (p.Asp1159His)
c.3478G>C (p.Asp1160His)
c.3316G>C (p.Asp1106His)
c.3349G>C (p.Asp1117His)
3g.38576694C>TCA352138392SCN5Ac.3475G>A (p.Asp1159Asn)
c.3478G>A (p.Asp1160Asn)
c.3316G>A (p.Asp1106Asn)
c.3349G>A (p.Asp1117Asn)
 COSMIC COSMIC COSMIC
3g.38576695C>ACA352138393SCN5Ac.3474G>T (p.Gln1158His)
c.3477G>T (p.Gln1159His)
c.3315G>T (p.Gln1105His)
c.3348G>T (p.Gln1116His)
 gnomAD v4
3g.38576695C>GCA352138394SCN5Ac.3474G>C (p.Gln1158His)
c.3477G>C (p.Gln1159His)
c.3315G>C (p.Gln1105His)
c.3348G>C (p.Gln1116His)
3g.38576695C>TCA433134134SCN5Ac.3474G>A (p.Gln1158=)
c.3477G>A (p.Gln1159=)
c.3315G>A (p.Gln1105=)
c.3348G>A (p.Gln1116=)
3g.38576696T>ACA352138397SCN5Ac.3473A>T (p.Gln1158Leu)
c.3476A>T (p.Gln1159Leu)
c.3314A>T (p.Gln1105Leu)
c.3347A>T (p.Gln1116Leu)
3g.38576696T>CCA352138395SCN5Ac.3473A>G (p.Gln1158Arg)
c.3476A>G (p.Gln1159Arg)
c.3314A>G (p.Gln1105Arg)
c.3347A>G (p.Gln1116Arg)
3g.38576696T>GCA352138396SCN5Ac.3473A>C (p.Gln1158Pro)
c.3476A>C (p.Gln1159Pro)
c.3314A>C (p.Gln1105Pro)
c.3347A>C (p.Gln1116Pro)
3g.38576697G>ACA352138398SCN5Ac.3472C>T (p.Gln1158Ter)
c.3475C>T (p.Gln1159Ter)
c.3313C>T (p.Gln1105Ter)
c.3346C>T (p.Gln1116Ter)
 gnomAD v4
3g.38576697G>CCA352138400SCN5Ac.3472C>G (p.Gln1158Glu)
c.3475C>G (p.Gln1159Glu)
c.3313C>G (p.Gln1105Glu)
c.3346C>G (p.Gln1116Glu)
3g.38576697G>TCA352138399SCN5Ac.3472C>A (p.Gln1158Lys)
c.3475C>A (p.Gln1159Lys)
c.3313C>A (p.Gln1105Lys)
c.3346C>A (p.Gln1116Lys)
3g.38576698G>ACA433134135SCN5Ac.3471C>T (p.Gly1157=)
c.3474C>T (p.Gly1158=)
c.3312C>T (p.Gly1104=)
c.3345C>T (p.Gly1115=)
 gnomAD v4
3g.38576698G>CCA433134136SCN5Ac.3471C>G (p.Gly1157=)
c.3474C>G (p.Gly1158=)
c.3312C>G (p.Gly1104=)
c.3345C>G (p.Gly1115=)
3g.38576698G>TCA433134137SCN5Ac.3471C>A (p.Gly1157=)
c.3474C>A (p.Gly1158=)
c.3312C>A (p.Gly1104=)
c.3345C>A (p.Gly1115=)
3g.38576699C>ACA352138401SCN5Ac.3470G>T (p.Gly1157Val)
c.3473G>T (p.Gly1158Val)
c.3311G>T (p.Gly1104Val)
c.3344G>T (p.Gly1115Val)
 ClinVar dbSNP
3g.38576699C=CA1358573160SCN5Ac.3470G= (p.Gly1157=)
c.3473G= (p.Gly1158=)
c.3311G= (p.Gly1104=)
c.3344G= (p.Gly1115=)
3g.38576699C>GCA352138402SCN5Ac.3470G>C (p.Gly1157Ala)
c.3473G>C (p.Gly1158Ala)
c.3311G>C (p.Gly1104Ala)
c.3344G>C (p.Gly1115Ala)
3g.38576699C>TCA352138403SCN5Ac.3470G>A (p.Gly1157Asp)
c.3473G>A (p.Gly1158Asp)
c.3311G>A (p.Gly1104Asp)
c.3344G>A (p.Gly1115Asp)
3g.38576700C>ACA352138404SCN5Ac.3469G>T (p.Gly1157Cys)
c.3472G>T (p.Gly1158Cys)
c.3310G>T (p.Gly1104Cys)
c.3343G>T (p.Gly1115Cys)
 dbSNP gnomAD v3 gnomAD v4
3g.38576700C=CA1358573161SCN5Ac.3469G= (p.Gly1157=)
c.3472G= (p.Gly1158=)
c.3310G= (p.Gly1104=)
c.3343G= (p.Gly1115=)
3g.38576700C>GCA352138405SCN5Ac.3469G>C (p.Gly1157Arg)
c.3472G>C (p.Gly1158Arg)
c.3310G>C (p.Gly1104Arg)
c.3343G>C (p.Gly1115Arg)
3g.38576700C>TCA352138406SCN5Ac.3469G>A (p.Gly1157Ser)
c.3472G>A (p.Gly1158Ser)
c.3310G>A (p.Gly1104Ser)
c.3343G>A (p.Gly1115Ser)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC
3g.38576701G>ACA061880SCN5Ac.3468C>T (p.Leu1156=)
c.3471C>T (p.Leu1157=)
c.3309C>T (p.Leu1103=)
c.3342C>T (p.Leu1114=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38576701G>CCA433134141SCN5Ac.3468C>G (p.Leu1156=)
c.3471C>G (p.Leu1157=)
c.3309C>G (p.Leu1103=)
c.3342C>G (p.Leu1114=)
3g.38576701G=CA1358573162SCN5Ac.3468C= (p.Leu1156=)
c.3471C= (p.Leu1157=)
c.3309C= (p.Leu1103=)
c.3342C= (p.Leu1114=)
3g.38576701G>TCA433134140SCN5Ac.3468C>A (p.Leu1156=)
c.3471C>A (p.Leu1157=)
c.3309C>A (p.Leu1103=)
c.3342C>A (p.Leu1114=)
3g.38576702A>CCA352138407SCN5Ac.3467T>G (p.Leu1156Arg)
c.3470T>G (p.Leu1157Arg)
c.3308T>G (p.Leu1103Arg)
c.3341T>G (p.Leu1114Arg)
3g.38576702A>GCA352138408SCN5Ac.3467T>C (p.Leu1156Pro)
c.3470T>C (p.Leu1157Pro)
c.3308T>C (p.Leu1103Pro)
c.3341T>C (p.Leu1114Pro)
3g.38576702A>TCA352138409SCN5Ac.3467T>A (p.Leu1156His)
c.3470T>A (p.Leu1157His)
c.3308T>A (p.Leu1103His)
c.3341T>A (p.Leu1114His)
3g.38576703G>ACA352138410SCN5Ac.3466C>T (p.Leu1156Phe)
c.3469C>T (p.Leu1157Phe)
c.3307C>T (p.Leu1103Phe)
c.3340C>T (p.Leu1114Phe)
 gnomAD v4
3g.38576703G>CCA352138411SCN5Ac.3466C>G (p.Leu1156Val)
c.3469C>G (p.Leu1157Val)
c.3307C>G (p.Leu1103Val)
c.3340C>G (p.Leu1114Val)
3g.38576703G>TCA352138412SCN5Ac.3466C>A (p.Leu1156Ile)
c.3469C>A (p.Leu1157Ile)
c.3307C>A (p.Leu1103Ile)
c.3340C>A (p.Leu1114Ile)
3g.38576704G>ACA433134144SCN5Ac.3465C>T (p.Asp1155=)
c.3468C>T (p.Asp1156=)
c.3306C>T (p.Asp1102=)
c.3339C>T (p.Asp1113=)
3g.38576704G>CCA352138413SCN5Ac.3465C>G (p.Asp1155Glu)
c.3468C>G (p.Asp1156Glu)
c.3306C>G (p.Asp1102Glu)
c.3339C>G (p.Asp1113Glu)
3g.38576704G>TCA352138414SCN5Ac.3465C>A (p.Asp1155Glu)
c.3468C>A (p.Asp1156Glu)
c.3306C>A (p.Asp1102Glu)
c.3339C>A (p.Asp1113Glu)
3g.38576705T>ACA352138415SCN5Ac.3464A>T (p.Asp1155Val)
c.3467A>T (p.Asp1156Val)
c.3305A>T (p.Asp1102Val)
c.3338A>T (p.Asp1113Val)
3g.38576705T>CCA017175SCN5Ac.3464A>G (p.Asp1155Gly)
c.3467A>G (p.Asp1156Gly)
c.3305A>G (p.Asp1102Gly)
c.3338A>G (p.Asp1113Gly)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38576705T>GCA352138416SCN5Ac.3464A>C (p.Asp1155Ala)
c.3467A>C (p.Asp1156Ala)
c.3305A>C (p.Asp1102Ala)
c.3338A>C (p.Asp1113Ala)
 ClinVar dbSNP gnomAD v3 gnomAD v4
3g.38576705T=CA1358573163SCN5Ac.3464A= (p.Asp1155=)
c.3467A= (p.Asp1156=)
c.3305A= (p.Asp1102=)
c.3338A= (p.Asp1113=)
3g.38576706C>ACA352138417SCN5Ac.3463G>T (p.Asp1155Tyr)
c.3466G>T (p.Asp1156Tyr)
c.3304G>T (p.Asp1102Tyr)
c.3337G>T (p.Asp1113Tyr)
3g.38576706C>GCA352138418SCN5Ac.3463G>C (p.Asp1155His)
c.3466G>C (p.Asp1156His)
c.3304G>C (p.Asp1102His)
c.3337G>C (p.Asp1113His)
3g.38576706C>TCA352138419SCN5Ac.3463G>A (p.Asp1155Asn)
c.3466G>A (p.Asp1156Asn)
c.3304G>A (p.Asp1102Asn)
c.3337G>A (p.Asp1113Asn)
3g.38576707A>CCA433134148SCN5Ac.3462T>G (p.Pro1154=)
c.3465T>G (p.Pro1155=)
c.3303T>G (p.Pro1101=)
c.3336T>G (p.Pro1112=)
3g.38576707A>GCA433134152SCN5Ac.3462T>C (p.Pro1154=)
c.3465T>C (p.Pro1155=)
c.3303T>C (p.Pro1101=)
c.3336T>C (p.Pro1112=)
3g.38576707A>TCA433134150SCN5Ac.3462T>A (p.Pro1154=)
c.3465T>A (p.Pro1155=)
c.3303T>A (p.Pro1101=)
c.3336T>A (p.Pro1112=)
3g.38576708G>ACA352138420SCN5Ac.3461C>T (p.Pro1154Leu)
c.3464C>T (p.Pro1155Leu)
c.3302C>T (p.Pro1101Leu)
c.3335C>T (p.Pro1112Leu)
3g.38576708G>CCA352138421SCN5Ac.3461C>G (p.Pro1154Arg)
c.3464C>G (p.Pro1155Arg)
c.3302C>G (p.Pro1101Arg)
c.3335C>G (p.Pro1112Arg)
3g.38576708G>TCA352138422SCN5Ac.3461C>A (p.Pro1154His)
c.3464C>A (p.Pro1155His)
c.3302C>A (p.Pro1101His)
c.3335C>A (p.Pro1112His)
3g.38576709G>ACA061870SCN5Ac.3460C>T (p.Pro1154Ser)
c.3463C>T (p.Pro1155Ser)
c.3301C>T (p.Pro1101Ser)
c.3334C>T (p.Pro1112Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38576709G>CCA352138423SCN5Ac.3460C>G (p.Pro1154Ala)
c.3463C>G (p.Pro1155Ala)
c.3301C>G (p.Pro1101Ala)
c.3334C>G (p.Pro1112Ala)
3g.38576709G=CA1358573164SCN5Ac.3460C= (p.Pro1154=)
c.3463C= (p.Pro1155=)
c.3301C= (p.Pro1101=)
c.3334C= (p.Pro1112=)
3g.38576709G>TCA352138424SCN5Ac.3460C>A (p.Pro1154Thr)
c.3463C>A (p.Pro1155Thr)
c.3301C>A (p.Pro1101Thr)
c.3334C>A (p.Pro1112Thr)
3g.38576710G>ACA433134154SCN5Ac.3459C>T (p.Ile1153=)
c.3462C>T (p.Ile1154=)
c.3300C>T (p.Ile1100=)
c.3333C>T (p.Ile1111=)
3g.38576710G>CCA352138425SCN5Ac.3459C>G (p.Ile1153Met)
c.3462C>G (p.Ile1154Met)
c.3300C>G (p.Ile1100Met)
c.3333C>G (p.Ile1111Met)
 ClinVar gnomAD v4
3g.38576710G>TCA433134155SCN5Ac.3459C>A (p.Ile1153=)
c.3462C>A (p.Ile1154=)
c.3300C>A (p.Ile1100=)
c.3333C>A (p.Ile1111=)
3g.38576711delCA2580614197SCN5Ac.3458del (p.Ile1153ThrfsTer?)
c.3461del (p.Ile1154ThrfsTer?)
c.3299del (p.Ile1100ThrfsTer?)
c.3332del (p.Ile1111ThrfsTer?)
 ClinVar
3g.38576711A=CA1358573165SCN5Ac.3458T= (p.Ile1153=)
c.3461T= (p.Ile1154=)
c.3299T= (p.Ile1100=)
c.3332T= (p.Ile1111=)
3g.38576711A>CCA352138426SCN5Ac.3458T>G (p.Ile1153Ser)
c.3461T>G (p.Ile1154Ser)
c.3299T>G (p.Ile1100Ser)
c.3332T>G (p.Ile1111Ser)
3g.38576711A>GCA352138427SCN5Ac.3458T>C (p.Ile1153Thr)
c.3461T>C (p.Ile1154Thr)
c.3299T>C (p.Ile1100Thr)
c.3332T>C (p.Ile1111Thr)
 ClinVar
3g.38576711A>TCA72923955SCN5Ac.3458T>A (p.Ile1153Asn)
c.3461T>A (p.Ile1154Asn)
c.3299T>A (p.Ile1100Asn)
c.3332T>A (p.Ile1111Asn)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.38576712T>ACA352138428SCN5Ac.3457A>T (p.Ile1153Phe)
c.3460A>T (p.Ile1154Phe)
c.3298A>T (p.Ile1100Phe)
c.3331A>T (p.Ile1111Phe)
 ClinVar
3g.38576712T>CCA352138429SCN5Ac.3457A>G (p.Ile1153Val)
c.3460A>G (p.Ile1154Val)
c.3298A>G (p.Ile1100Val)
c.3331A>G (p.Ile1111Val)
3g.38576712T>GCA352138430SCN5Ac.3457A>C (p.Ile1153Leu)
c.3460A>C (p.Ile1154Leu)
c.3298A>C (p.Ile1100Leu)
c.3331A>C (p.Ile1111Leu)
3g.38576713C>ACA352138431SCN5Ac.3456G>T (p.Gln1152His)
c.3459G>T (p.Gln1153His)
c.3297G>T (p.Gln1099His)
c.3330G>T (p.Gln1110His)
3g.38576713C=CA1358573166SCN5Ac.3456G= (p.Gln1152=)
c.3459G= (p.Gln1153=)
c.3297G= (p.Gln1099=)
c.3330G= (p.Gln1110=)
3g.38576713C>GCA061864SCN5Ac.3456G>C (p.Gln1152His)
c.3459G>C (p.Gln1153His)
c.3297G>C (p.Gln1099His)
c.3330G>C (p.Gln1110His)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38576713C>TCA433134160SCN5Ac.3456G>A (p.Gln1152=)
c.3459G>A (p.Gln1153=)
c.3297G>A (p.Gln1099=)
c.3330G>A (p.Gln1110=)
3g.38576714T>ACA352138432SCN5Ac.3455A>T (p.Gln1152Leu)
c.3458A>T (p.Gln1153Leu)
c.3296A>T (p.Gln1099Leu)
c.3329A>T (p.Gln1110Leu)
3g.38576714T>CCA352138433SCN5Ac.3455A>G (p.Gln1152Arg)
c.3458A>G (p.Gln1153Arg)
c.3296A>G (p.Gln1099Arg)
c.3329A>G (p.Gln1110Arg)
 gnomAD v4
3g.38576714T>GCA352138434SCN5Ac.3455A>C (p.Gln1152Pro)
c.3458A>C (p.Gln1153Pro)
c.3296A>C (p.Gln1099Pro)
c.3329A>C (p.Gln1110Pro)
3g.38576715G>ACA352138435SCN5Ac.3454C>T (p.Gln1152Ter)
c.3457C>T (p.Gln1153Ter)
c.3295C>T (p.Gln1099Ter)
c.3328C>T (p.Gln1110Ter)
 ClinVar dbSNP
3g.38576715G>CCA352138436SCN5Ac.3454C>G (p.Gln1152Glu)
c.3457C>G (p.Gln1153Glu)
c.3295C>G (p.Gln1099Glu)
c.3328C>G (p.Gln1110Glu)
 ClinVar dbSNP
3g.38576715G=CA1358573167SCN5Ac.3454C= (p.Gln1152=)
c.3457C= (p.Gln1153=)
c.3295C= (p.Gln1099=)
c.3328C= (p.Gln1110=)
3g.38576715G>TCA352138437SCN5Ac.3454C>A (p.Gln1152Lys)
c.3457C>A (p.Gln1153Lys)
c.3295C>A (p.Gln1099Lys)
c.3328C>A (p.Gln1110Lys)
3g.38576716C>ACA352138438SCN5Ac.3453G>T (p.Glu1151Asp)
c.3456G>T (p.Glu1152Asp)
c.3294G>T (p.Glu1098Asp)
c.3327G>T (p.Glu1109Asp)
3g.38576716C>GCA352138439SCN5Ac.3453G>C (p.Glu1151Asp)
c.3456G>C (p.Glu1152Asp)
c.3294G>C (p.Glu1098Asp)
c.3327G>C (p.Glu1109Asp)
3g.38576716C>TCA433134161SCN5Ac.3453G>A (p.Glu1151=)
c.3456G>A (p.Glu1152=)
c.3294G>A (p.Glu1098=)
c.3327G>A (p.Glu1109=)
3g.38576717T>ACA352138442SCN5Ac.3452A>T (p.Glu1151Val)
c.3455A>T (p.Glu1152Val)
c.3293A>T (p.Glu1098Val)
c.3326A>T (p.Glu1109Val)
3g.38576717T>CCA352138440SCN5Ac.3452A>G (p.Glu1151Gly)
c.3455A>G (p.Glu1152Gly)
c.3293A>G (p.Glu1098Gly)
c.3326A>G (p.Glu1109Gly)
3g.38576717T>GCA352138441SCN5Ac.3452A>C (p.Glu1151Ala)
c.3455A>C (p.Glu1152Ala)
c.3293A>C (p.Glu1098Ala)
c.3326A>C (p.Glu1109Ala)
3g.38576718C>ACA352138443SCN5Ac.3451G>T (p.Glu1151Ter)
c.3454G>T (p.Glu1152Ter)
c.3292G>T (p.Glu1098Ter)
c.3325G>T (p.Glu1109Ter)
 dbSNP
3g.38576718C=CA1358573168SCN5Ac.3451G= (p.Glu1151=)
c.3454G= (p.Glu1152=)
c.3292G= (p.Glu1098=)
c.3325G= (p.Glu1109=)
3g.38576718C>GCA352138444SCN5Ac.3451G>C (p.Glu1151Gln)
c.3454G>C (p.Glu1152Gln)
c.3292G>C (p.Glu1098Gln)
c.3325G>C (p.Glu1109Gln)
3g.38576718C>TCA352138445SCN5Ac.3451G>A (p.Glu1151Lys)
c.3454G>A (p.Glu1152Lys)
c.3292G>A (p.Glu1098Lys)
c.3325G>A (p.Glu1109Lys)
3g.38576719C>ACA433134163SCN5Ac.3450G>T (p.Leu1150=)
c.3453G>T (p.Leu1151=)
c.3291G>T (p.Leu1097=)
c.3324G>T (p.Leu1108=)
3g.38576719C=CA1358573169SCN5Ac.3450G= (p.Leu1150=)
c.3453G= (p.Leu1151=)
c.3291G= (p.Leu1097=)
c.3324G= (p.Leu1108=)
3g.38576719C>GCA433134164SCN5Ac.3450G>C (p.Leu1150=)
c.3453G>C (p.Leu1151=)
c.3291G>C (p.Leu1097=)
c.3324G>C (p.Leu1108=)
3g.38576719C>TCA433134165SCN5Ac.3450G>A (p.Leu1150=)
c.3453G>A (p.Leu1151=)
c.3291G>A (p.Leu1097=)
c.3324G>A (p.Leu1108=)
 dbSNP gnomAD v3 gnomAD v4
3g.38576720A>CCA352138446SCN5Ac.3449T>G (p.Leu1150Arg)
c.3452T>G (p.Leu1151Arg)
c.3290T>G (p.Leu1097Arg)
c.3323T>G (p.Leu1108Arg)
3g.38576720A>GCA352138447SCN5Ac.3449T>C (p.Leu1150Pro)
c.3452T>C (p.Leu1151Pro)
c.3290T>C (p.Leu1097Pro)
c.3323T>C (p.Leu1108Pro)
 gnomAD v4
3g.38576720A>TCA352138448SCN5Ac.3449T>A (p.Leu1150Gln)
c.3452T>A (p.Leu1151Gln)
c.3290T>A (p.Leu1097Gln)
c.3323T>A (p.Leu1108Gln)
3g.38576721G>ACA433134168SCN5Ac.3448C>T (p.Leu1150=)
c.3451C>T (p.Leu1151=)
c.3289C>T (p.Leu1097=)
c.3322C>T (p.Leu1108=)
 dbSNP gnomAD v2 gnomAD v4
3g.38576721G>CCA352138449SCN5Ac.3448C>G (p.Leu1150Val)
c.3451C>G (p.Leu1151Val)
c.3289C>G (p.Leu1097Val)
c.3322C>G (p.Leu1108Val)
3g.38576721G=CA1358573170SCN5Ac.3448C= (p.Leu1150=)
c.3451C= (p.Leu1151=)
c.3289C= (p.Leu1097=)
c.3322C= (p.Leu1108=)
3g.38576721G>TCA352138450SCN5Ac.3448C>A (p.Leu1150Met)
c.3451C>A (p.Leu1151Met)
c.3289C>A (p.Leu1097Met)
c.3322C>A (p.Leu1108Met)
3g.38576722G>ACA433134170SCN5Ac.3447C>T (p.Leu1149=)
c.3450C>T (p.Leu1150=)
c.3288C>T (p.Leu1096=)
c.3321C>T (p.Leu1107=)
3g.38576722G>CCA433134171SCN5Ac.3447C>G (p.Leu1149=)
c.3450C>G (p.Leu1150=)
c.3288C>G (p.Leu1096=)
c.3321C>G (p.Leu1107=)
3g.38576722G>TCA433134169SCN5Ac.3447C>A (p.Leu1149=)
c.3450C>A (p.Leu1150=)
c.3288C>A (p.Leu1096=)
c.3321C>A (p.Leu1107=)
3g.38576723A>CCA352138451SCN5Ac.3446T>G (p.Leu1149Arg)
c.3449T>G (p.Leu1150Arg)
c.3287T>G (p.Leu1096Arg)
c.3320T>G (p.Leu1107Arg)
3g.38576723A>GCA352138452SCN5Ac.3446T>C (p.Leu1149Pro)
c.3449T>C (p.Leu1150Pro)
c.3287T>C (p.Leu1096Pro)
c.3320T>C (p.Leu1107Pro)
3g.38576723A>TCA352138453SCN5Ac.3446T>A (p.Leu1149His)
c.3449T>A (p.Leu1150His)
c.3287T>A (p.Leu1096His)
c.3320T>A (p.Leu1107His)
3g.38576724G>ACA352138454SCN5Ac.3445C>T (p.Leu1149Phe)
c.3448C>T (p.Leu1150Phe)
c.3286C>T (p.Leu1096Phe)
c.3319C>T (p.Leu1107Phe)
 dbSNP
3g.38576724G>CCA352138456SCN5Ac.3445C>G (p.Leu1149Val)
c.3448C>G (p.Leu1150Val)
c.3286C>G (p.Leu1096Val)
c.3319C>G (p.Leu1107Val)
3g.38576724G>TCA352138455SCN5Ac.3445C>A (p.Leu1149Ile)
c.3448C>A (p.Leu1150Ile)
c.3286C>A (p.Leu1096Ile)
c.3319C>A (p.Leu1107Ile)
3g.38576725C>ACA352138457SCN5Ac.3444G>T (p.Glu1148Asp)
c.3447G>T (p.Glu1149Asp)
c.3285G>T (p.Glu1095Asp)
c.3318G>T (p.Glu1106Asp)
3g.38576725C=CA1358573171SCN5Ac.3444G= (p.Glu1148=)
c.3447G= (p.Glu1149=)
c.3285G= (p.Glu1095=)
c.3318G= (p.Glu1106=)
3g.38576725C>GCA352138458SCN5Ac.3444G>C (p.Glu1148Asp)
c.3447G>C (p.Glu1149Asp)
c.3285G>C (p.Glu1095Asp)
c.3318G>C (p.Glu1106Asp)
3g.38576725C>TCA433134174SCN5Ac.3444G>A (p.Glu1148=)
c.3447G>A (p.Glu1149=)
c.3285G>A (p.Glu1095=)
c.3318G>A (p.Glu1106=)
 dbSNP gnomAD v3 gnomAD v4
3g.38576726T>ACA352138459SCN5Ac.3443A>T (p.Glu1148Val)
c.3446A>T (p.Glu1149Val)
c.3284A>T (p.Glu1095Val)
c.3317A>T (p.Glu1106Val)
3g.38576726T>CCA352138461SCN5Ac.3443A>G (p.Glu1148Gly)
c.3446A>G (p.Glu1149Gly)
c.3284A>G (p.Glu1095Gly)
c.3317A>G (p.Glu1106Gly)
3g.38576726T>GCA352138460SCN5Ac.3443A>C (p.Glu1148Ala)
c.3446A>C (p.Glu1149Ala)
c.3284A>C (p.Glu1095Ala)
c.3317A>C (p.Glu1106Ala)
3g.38576727C>ACA352138462SCN5Ac.3442G>T (p.Glu1148Ter)
c.3445G>T (p.Glu1149Ter)
c.3283G>T (p.Glu1095Ter)
c.3316G>T (p.Glu1106Ter)
 dbSNP
3g.38576727C=CA1358573172SCN5Ac.3442G= (p.Glu1148=)
c.3445G= (p.Glu1149=)
c.3283G= (p.Glu1095=)
c.3316G= (p.Glu1106=)
3g.38576727C>GCA352138463SCN5Ac.3442G>C (p.Glu1148Gln)
c.3445G>C (p.Glu1149Gln)
c.3283G>C (p.Glu1095Gln)
c.3316G>C (p.Glu1106Gln)
3g.38576727C>TCA352138464SCN5Ac.3442G>A (p.Glu1148Lys)
c.3445G>A (p.Glu1149Lys)
c.3283G>A (p.Glu1095Lys)
c.3316G>A (p.Glu1106Lys)
3g.38576728A>CCA433134176SCN5Ac.3441T>G (p.Ala1147=)
c.3444T>G (p.Ala1148=)
c.3282T>G (p.Ala1094=)
c.3315T>G (p.Ala1105=)
3g.38576728A>GCA433134177SCN5Ac.3441T>C (p.Ala1147=)
c.3444T>C (p.Ala1148=)
c.3282T>C (p.Ala1094=)
c.3315T>C (p.Ala1105=)
3g.38576728A>TCA433134178SCN5Ac.3441T>A (p.Ala1147=)
c.3444T>A (p.Ala1148=)
c.3282T>A (p.Ala1094=)
c.3315T>A (p.Ala1105=)
3g.38576729G>ACA352138465SCN5Ac.3440C>T (p.Ala1147Val)
c.3443C>T (p.Ala1148Val)
c.3281C>T (p.Ala1094Val)
c.3314C>T (p.Ala1105Val)
3g.38576729G>CCA352138466SCN5Ac.3440C>G (p.Ala1147Gly)
c.3443C>G (p.Ala1148Gly)
c.3281C>G (p.Ala1094Gly)
c.3314C>G (p.Ala1105Gly)
3g.38576729G>TCA352138467SCN5Ac.3440C>A (p.Ala1147Asp)
c.3443C>A (p.Ala1148Asp)
c.3281C>A (p.Ala1094Asp)
c.3314C>A (p.Ala1105Asp)
3g.38576730C>ACA061854SCN5Ac.3439G>T (p.Ala1147Ser)
c.3442G>T (p.Ala1148Ser)
c.3280G>T (p.Ala1094Ser)
c.3313G>T (p.Ala1105Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.38576730C=CA1358573173SCN5Ac.3439G= (p.Ala1147=)
c.3442G= (p.Ala1148=)
c.3280G= (p.Ala1094=)
c.3313G= (p.Ala1105=)
3g.38576730C>GCA352138468SCN5Ac.3439G>C (p.Ala1147Pro)
c.3442G>C (p.Ala1148Pro)
c.3280G>C (p.Ala1094Pro)
c.3313G>C (p.Ala1105Pro)
 ClinVar dbSNP
3g.38576730C>TCA061848SCN5Ac.3439G>A (p.Ala1147Thr)
c.3442G>A (p.Ala1148Thr)
c.3280G>A (p.Ala1094Thr)
c.3313G>A (p.Ala1105Thr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38576731G>ACA061843SCN5Ac.3438C>T (p.Thr1146=)
c.3441C>T (p.Thr1147=)
c.3279C>T (p.Thr1093=)
c.3312C>T (p.Thr1104=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.38576731G>CCA433134180SCN5Ac.3438C>G (p.Thr1146=)
c.3441C>G (p.Thr1147=)
c.3279C>G (p.Thr1093=)
c.3312C>G (p.Thr1104=)
3g.38576731G=CA1358573174SCN5Ac.3438C= (p.Thr1146=)
c.3441C= (p.Thr1147=)
c.3279C= (p.Thr1093=)
c.3312C= (p.Thr1104=)
3g.38576731G>TCA433134181SCN5Ac.3438C>A (p.Thr1146=)
c.3441C>A (p.Thr1147=)
c.3279C>A (p.Thr1093=)
c.3312C>A (p.Thr1104=)
 gnomAD v4
3g.38576732G>ACA061838SCN5Ac.3437C>T (p.Thr1146Ile)
c.3440C>T (p.Thr1147Ile)
c.3278C>T (p.Thr1093Ile)
c.3311C>T (p.Thr1104Ile)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.38576732G>CCA72923967SCN5Ac.3437C>G (p.Thr1146Ser)
c.3440C>G (p.Thr1147Ser)
c.3278C>G (p.Thr1093Ser)
c.3311C>G (p.Thr1104Ser)
 ClinVar dbSNP gnomAD v2 gnomAD v4
3g.38576732G=CA1358573175SCN5Ac.3437C= (p.Thr1146=)
c.3440C= (p.Thr1147=)
c.3278C= (p.Thr1093=)
c.3311C= (p.Thr1104=)
3g.38576732G>TCA061831SCN5Ac.3437C>A (p.Thr1146Asn)
c.3440C>A (p.Thr1147Asn)
c.3278C>A (p.Thr1093Asn)
c.3311C>A (p.Thr1104Asn)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC
3g.38576733T>ACA352138469SCN5Ac.3436A>T (p.Thr1146Ser)
c.3439A>T (p.Thr1147Ser)
c.3277A>T (p.Thr1093Ser)
c.3310A>T (p.Thr1104Ser)
3g.38576733T>CCA017161SCN5Ac.3436A>G (p.Thr1146Ala)
c.3439A>G (p.Thr1147Ala)
c.3277A>G (p.Thr1093Ala)
c.3310A>G (p.Thr1104Ala)
 ClinVar dbSNP gnomAD v4
3g.38576733T>GCA352138470SCN5Ac.3436A>C (p.Thr1146Pro)
c.3439A>C (p.Thr1147Pro)
c.3277A>C (p.Thr1093Pro)
c.3310A>C (p.Thr1104Pro)
3g.38576733T=CA1358573176SCN5Ac.3436A= (p.Thr1146=)
c.3439A= (p.Thr1147=)
c.3277A= (p.Thr1093=)
c.3310A= (p.Thr1104=)
3g.38576734delCA2586972096SCN5Ac.3435del (p.Asn1145LysfsTer?)
c.3438del (p.Asn1146LysfsTer?)
c.3276del (p.Asn1092LysfsTer?)
c.3309del (p.Asn1103LysfsTer?)
3g.38576734G>ACA433134182SCN5Ac.3435C>T (p.Asn1145=)
c.3438C>T (p.Asn1146=)
c.3276C>T (p.Asn1092=)
c.3309C>T (p.Asn1103=)
 ClinVar gnomAD v4 COSMIC COSMIC COSMIC
3g.38576734G>CCA352138471SCN5Ac.3435C>G (p.Asn1145Lys)
c.3438C>G (p.Asn1146Lys)
c.3276C>G (p.Asn1092Lys)
c.3309C>G (p.Asn1103Lys)
3g.38576734G=CA1358573177SCN5Ac.3435C= (p.Asn1145=)
c.3438C= (p.Asn1146=)
c.3276C= (p.Asn1092=)
c.3309C= (p.Asn1103=)
3g.38576734G>TCA352138472SCN5Ac.3435C>A (p.Asn1145Lys)
c.3438C>A (p.Asn1146Lys)
c.3276C>A (p.Asn1092Lys)
c.3309C>A (p.Asn1103Lys)
3g.38576734_38576735insACA352138473SCN5Ac.3434_3435insT (p.Thr1146HisfsTer3)
c.3437_3438insT (p.Thr1147HisfsTer3)
c.3275_3276insT (p.Thr1093HisfsTer3)
c.3308_3309insT (p.Thr1104HisfsTer3)
 dbSNP
3g.38576735T>ACA352138474SCN5Ac.3434A>T (p.Asn1145Ile)
c.3437A>T (p.Asn1146Ile)
c.3275A>T (p.Asn1092Ile)
c.3308A>T (p.Asn1103Ile)
3g.38576735T>CCA352138475SCN5Ac.3434A>G (p.Asn1145Ser)
c.3437A>G (p.Asn1146Ser)
c.3275A>G (p.Asn1092Ser)
c.3308A>G (p.Asn1103Ser)
3g.38576735T>GCA352138476SCN5Ac.3434A>C (p.Asn1145Thr)
c.3437A>C (p.Asn1146Thr)
c.3275A>C (p.Asn1092Thr)
c.3308A>C (p.Asn1103Thr)
3g.38576736T>ACA352138477SCN5Ac.3433A>T (p.Asn1145Tyr)
c.3436A>T (p.Asn1146Tyr)
c.3274A>T (p.Asn1092Tyr)
c.3307A>T (p.Asn1103Tyr)
3g.38576736T>CCA352138478SCN5Ac.3433A>G (p.Asn1145Asp)
c.3436A>G (p.Asn1146Asp)
c.3274A>G (p.Asn1092Asp)
c.3307A>G (p.Asn1103Asp)
 dbSNP
3g.38576736T>GCA352138479SCN5Ac.3433A>C (p.Asn1145His)
c.3436A>C (p.Asn1146His)
c.3274A>C (p.Asn1092His)
c.3307A>C (p.Asn1103His)
3g.38576736T=CA1358573178SCN5Ac.3433A= (p.Asn1145=)
c.3436A= (p.Asn1146=)
c.3274A= (p.Asn1092=)
c.3307A= (p.Asn1103=)
3g.38576737G>ACA061826SCN5Ac.3432C>T (p.Thr1144=)
c.3435C>T (p.Thr1145=)
c.3273C>T (p.Thr1091=)
c.3306C>T (p.Thr1102=)
 ClinVar dbSNP ExAC gnomAD v2
3g.38576737G>CCA433134183SCN5Ac.3432C>G (p.Thr1144=)
c.3435C>G (p.Thr1145=)
c.3273C>G (p.Thr1091=)
c.3306C>G (p.Thr1102=)
3g.38576737G=CA1358573179SCN5Ac.3432C= (p.Thr1144=)
c.3435C= (p.Thr1145=)
c.3273C= (p.Thr1091=)
c.3306C= (p.Thr1102=)
3g.38576737G>TCA433134184SCN5Ac.3432C>A (p.Thr1144=)
c.3435C>A (p.Thr1145=)
c.3273C>A (p.Thr1091=)
c.3306C>A (p.Thr1102=)
3g.38576738G>ACA352138482SCN5Ac.3431C>T (p.Thr1144Ile)
c.3434C>T (p.Thr1145Ile)
c.3272C>T (p.Thr1091Ile)
c.3305C>T (p.Thr1102Ile)
 ClinVar dbSNP COSMIC COSMIC COSMIC
3g.38576738G>CCA352138481SCN5Ac.3431C>G (p.Thr1144Ser)
c.3434C>G (p.Thr1145Ser)
c.3272C>G (p.Thr1091Ser)
c.3305C>G (p.Thr1102Ser)
3g.38576738G=CA1358573180SCN5Ac.3431C= (p.Thr1144=)
c.3434C= (p.Thr1145=)
c.3272C= (p.Thr1091=)
c.3305C= (p.Thr1102=)
3g.38576738G>TCA352138480SCN5Ac.3431C>A (p.Thr1144Asn)
c.3434C>A (p.Thr1145Asn)
c.3272C>A (p.Thr1091Asn)
c.3305C>A (p.Thr1102Asn)
3g.38576739T>ACA352138485SCN5Ac.3430A>T (p.Thr1144Ser)
c.3433A>T (p.Thr1145Ser)
c.3271A>T (p.Thr1091Ser)
c.3304A>T (p.Thr1102Ser)
3g.38576739T>CCA352138483SCN5Ac.3430A>G (p.Thr1144Ala)
c.3433A>G (p.Thr1145Ala)
c.3271A>G (p.Thr1091Ala)
c.3304A>G (p.Thr1102Ala)
3g.38576739T>GCA352138484SCN5Ac.3430A>C (p.Thr1144Pro)
c.3433A>C (p.Thr1145Pro)
c.3271A>C (p.Thr1091Pro)
c.3304A>C (p.Thr1102Pro)
3g.38576740C>ACA352138486SCN5Ac.3429G>T (p.Met1143Ile)
c.3432G>T (p.Met1144Ile)
c.3270G>T (p.Met1090Ile)
c.3303G>T (p.Met1101Ile)
 COSMIC COSMIC COSMIC
3g.38576740C>GCA352138487SCN5Ac.3429G>C (p.Met1143Ile)
c.3432G>C (p.Met1144Ile)
c.3270G>C (p.Met1090Ile)
c.3303G>C (p.Met1101Ile)
3g.38576740C>TCA352138488SCN5Ac.3429G>A (p.Met1143Ile)
c.3432G>A (p.Met1144Ile)
c.3270G>A (p.Met1090Ile)
c.3303G>A (p.Met1101Ile)
3g.38576741_38576758dupCA2665112490SCN5Ac.3412_3429dup (p.Met1143_Thr1144insGlySerThrAlaAspMet)
c.3415_3432dup (p.Met1144_Thr1145insGlySerThrAlaAspMet)
c.3253_3270dup (p.Met1090_Thr1091insGlySerThrAlaAspMet)
c.3286_3303dup (p.Met1101_Thr1102insGlySerThrAlaAspMet)
 gnomAD v4
3g.38576741A=CA1358573181SCN5Ac.3428T= (p.Met1143=)
c.3431T= (p.Met1144=)
c.3269T= (p.Met1090=)
c.3302T= (p.Met1101=)
3g.38576741A>CCA352138489SCN5Ac.3428T>G (p.Met1143Arg)
c.3431T>G (p.Met1144Arg)
c.3269T>G (p.Met1090Arg)
c.3302T>G (p.Met1101Arg)
 dbSNP gnomAD v4
3g.38576741A>GCA352138490SCN5Ac.3428T>C (p.Met1143Thr)
c.3431T>C (p.Met1144Thr)
c.3269T>C (p.Met1090Thr)
c.3302T>C (p.Met1101Thr)
 gnomAD v4
3g.38576741A>TCA352138491SCN5Ac.3428T>A (p.Met1143Lys)
c.3431T>A (p.Met1144Lys)
c.3269T>A (p.Met1090Lys)
c.3302T>A (p.Met1101Lys)
3g.38576742T>ACA352138492SCN5Ac.3427A>T (p.Met1143Leu)
c.3430A>T (p.Met1144Leu)
c.3268A>T (p.Met1090Leu)
c.3301A>T (p.Met1101Leu)
3g.38576742T>CCA352138493SCN5Ac.3427A>G (p.Met1143Val)
c.3430A>G (p.Met1144Val)
c.3268A>G (p.Met1090Val)
c.3301A>G (p.Met1101Val)
 dbSNP
3g.38576742T>GCA352138494SCN5Ac.3427A>C (p.Met1143Leu)
c.3430A>C (p.Met1144Leu)
c.3268A>C (p.Met1090Leu)
c.3301A>C (p.Met1101Leu)
3g.38576742T=CA1358573182SCN5Ac.3427A= (p.Met1143=)
c.3430A= (p.Met1144=)
c.3268A= (p.Met1090=)
c.3301A= (p.Met1101=)
3g.38576743G>ACA433134187SCN5Ac.3426C>T (p.Asp1142=)
c.3429C>T (p.Asp1143=)
c.3267C>T (p.Asp1089=)
c.3300C>T (p.Asp1100=)
 dbSNP
3g.38576743G>CCA352138495SCN5Ac.3426C>G (p.Asp1142Glu)
c.3429C>G (p.Asp1143Glu)
c.3267C>G (p.Asp1089Glu)
c.3300C>G (p.Asp1100Glu)
3g.38576743G=CA1358573183SCN5Ac.3426C= (p.Asp1142=)
c.3429C= (p.Asp1143=)
c.3267C= (p.Asp1089=)
c.3300C= (p.Asp1100=)
3g.38576743G>TCA352138496SCN5Ac.3426C>A (p.Asp1142Glu)
c.3429C>A (p.Asp1143Glu)
c.3267C>A (p.Asp1089Glu)
c.3300C>A (p.Asp1100Glu)
3g.38576744T>ACA352138499SCN5Ac.3425A>T (p.Asp1142Val)
c.3428A>T (p.Asp1143Val)
c.3266A>T (p.Asp1089Val)
c.3299A>T (p.Asp1100Val)
 gnomAD v4
3g.38576744T>CCA352138497SCN5Ac.3425A>G (p.Asp1142Gly)
c.3428A>G (p.Asp1143Gly)
c.3266A>G (p.Asp1089Gly)
c.3299A>G (p.Asp1100Gly)
3g.38576744T>GCA352138498SCN5Ac.3425A>C (p.Asp1142Ala)
c.3428A>C (p.Asp1143Ala)
c.3266A>C (p.Asp1089Ala)
c.3299A>C (p.Asp1100Ala)
3g.38576745C>ACA352138500SCN5Ac.3424G>T (p.Asp1142Tyr)
c.3427G>T (p.Asp1143Tyr)
c.3265G>T (p.Asp1089Tyr)
c.3298G>T (p.Asp1100Tyr)
 gnomAD v4
3g.38576745C>GCA352138501SCN5Ac.3424G>C (p.Asp1142His)
c.3427G>C (p.Asp1143His)
c.3265G>C (p.Asp1089His)
c.3298G>C (p.Asp1100His)
3g.38576745C>TCA352138502SCN5Ac.3424G>A (p.Asp1142Asn)
c.3427G>A (p.Asp1143Asn)
c.3265G>A (p.Asp1089Asn)
c.3298G>A (p.Asp1100Asn)
3g.38576746T>ACA433134194SCN5Ac.3423A>T (p.Ala1141=)
c.3426A>T (p.Ala1142=)
c.3264A>T (p.Ala1088=)
c.3297A>T (p.Ala1099=)
3g.38576746T>CCA433134193SCN5Ac.3423A>G (p.Ala1141=)
c.3426A>G (p.Ala1142=)
c.3264A>G (p.Ala1088=)
c.3297A>G (p.Ala1099=)
3g.38576746T>GCA433134192SCN5Ac.3423A>C (p.Ala1141=)
c.3426A>C (p.Ala1142=)
c.3264A>C (p.Ala1088=)
c.3297A>C (p.Ala1099=)
3g.38576747G>ACA10585977SCN5Ac.3422C>T (p.Ala1141Val)
c.3425C>T (p.Ala1142Val)
c.3263C>T (p.Ala1088Val)
c.3296C>T (p.Ala1099Val)
 ClinVar dbSNP
3g.38576747G>CCA352138503SCN5Ac.3422C>G (p.Ala1141Gly)
c.3425C>G (p.Ala1142Gly)
c.3263C>G (p.Ala1088Gly)
c.3296C>G (p.Ala1099Gly)
3g.38576747G=CA1358573184SCN5Ac.3422C= (p.Ala1141=)
c.3425C= (p.Ala1142=)
c.3263C= (p.Ala1088=)
c.3296C= (p.Ala1099=)
3g.38576747G>TCA352138504SCN5Ac.3422C>A (p.Ala1141Glu)
c.3425C>A (p.Ala1142Glu)
c.3263C>A (p.Ala1088Glu)
c.3296C>A (p.Ala1099Glu)
3g.38576748C>ACA352138505SCN5Ac.3421G>T (p.Ala1141Ser)
c.3424G>T (p.Ala1142Ser)
c.3262G>T (p.Ala1088Ser)
c.3295G>T (p.Ala1099Ser)
3g.38576748C>GCA352138506SCN5Ac.3421G>C (p.Ala1141Pro)
c.3424G>C (p.Ala1142Pro)
c.3262G>C (p.Ala1088Pro)
c.3295G>C (p.Ala1099Pro)
3g.38576748C>TCA352138507SCN5Ac.3421G>A (p.Ala1141Thr)
c.3424G>A (p.Ala1142Thr)
c.3262G>A (p.Ala1088Thr)
c.3295G>A (p.Ala1099Thr)
3g.38576749T>ACA433134197SCN5Ac.3420A>T (p.Thr1140=)
c.3423A>T (p.Thr1141=)
c.3261A>T (p.Thr1087=)
c.3294A>T (p.Thr1098=)
3g.38576749T>CCA433134199SCN5Ac.3420A>G (p.Thr1140=)
c.3423A>G (p.Thr1141=)
c.3261A>G (p.Thr1087=)
c.3294A>G (p.Thr1098=)
 gnomAD v4
3g.38576749T>GCA433134198SCN5Ac.3420A>C (p.Thr1140=)
c.3423A>C (p.Thr1141=)
c.3261A>C (p.Thr1087=)
c.3294A>C (p.Thr1098=)
3g.38576750G>ACA352138508SCN5Ac.3419C>T (p.Thr1140Ile)
c.3422C>T (p.Thr1141Ile)
c.3260C>T (p.Thr1087Ile)
c.3293C>T (p.Thr1098Ile)
3g.38576750G>CCA352138509SCN5Ac.3419C>G (p.Thr1140Arg)
c.3422C>G (p.Thr1141Arg)
c.3260C>G (p.Thr1087Arg)
c.3293C>G (p.Thr1098Arg)
3g.38576750G>TCA352138510SCN5Ac.3419C>A (p.Thr1140Lys)
c.3422C>A (p.Thr1141Lys)
c.3260C>A (p.Thr1087Lys)
c.3293C>A (p.Thr1098Lys)
 gnomAD v4
3g.38576751T>ACA352138512SCN5Ac.3418A>T (p.Thr1140Ser)
c.3421A>T (p.Thr1141Ser)
c.3259A>T (p.Thr1087Ser)
c.3292A>T (p.Thr1098Ser)
 ClinVar
3g.38576751T>CCA352138513SCN5Ac.3418A>G (p.Thr1140Ala)
c.3421A>G (p.Thr1141Ala)
c.3259A>G (p.Thr1087Ala)
c.3292A>G (p.Thr1098Ala)
3g.38576751T>GCA352138511SCN5Ac.3418A>C (p.Thr1140Pro)
c.3421A>C (p.Thr1141Pro)
c.3259A>C (p.Thr1087Pro)
c.3292A>C (p.Thr1098Pro)
3g.38576754_38576756dupCA2580614198SCN5Ac.3416_3418dup (p.Ser1139_Thr1140insSer)
c.3419_3421dup (p.Ser1140_Thr1141insSer)
c.3257_3259dup (p.Ser1086_Thr1087insSer)
c.3290_3292dup (p.Ser1097_Thr1098insSer)
 ClinVar
3g.38576752G>ACA433134204SCN5Ac.3417C>T (p.Ser1139=)
c.3420C>T (p.Ser1140=)
c.3258C>T (p.Ser1086=)
c.3291C>T (p.Ser1097=)
 gnomAD v4
3g.38576752G>CCA352138514SCN5Ac.3417C>G (p.Ser1139Arg)
c.3420C>G (p.Ser1140Arg)
c.3258C>G (p.Ser1086Arg)
c.3291C>G (p.Ser1097Arg)
3g.38576752G>TCA352138515SCN5Ac.3417C>A (p.Ser1139Arg)
c.3420C>A (p.Ser1140Arg)
c.3258C>A (p.Ser1086Arg)
c.3291C>A (p.Ser1097Arg)
3g.38576753C>ACA352138516SCN5Ac.3416G>T (p.Ser1139Ile)
c.3419G>T (p.Ser1140Ile)
c.3257G>T (p.Ser1086Ile)
c.3290G>T (p.Ser1097Ile)
3g.38576753C=CA1358573185SCN5Ac.3416G= (p.Ser1139=)
c.3419G= (p.Ser1140=)
c.3257G= (p.Ser1086=)
c.3290G= (p.Ser1097=)
3g.38576753C>GCA017152SCN5Ac.3416G>C (p.Ser1139Thr)
c.3419G>C (p.Ser1140Thr)
c.3257G>C (p.Ser1086Thr)
c.3290G>C (p.Ser1097Thr)
 ClinVar dbSNP
3g.38576753C>TCA352138517SCN5Ac.3416G>A (p.Ser1139Asn)
c.3419G>A (p.Ser1140Asn)
c.3257G>A (p.Ser1086Asn)
c.3290G>A (p.Ser1097Asn)
 dbSNP gnomAD v4 COSMIC COSMIC COSMIC
3g.38576754T>ACA352138518SCN5Ac.3415A>T (p.Ser1139Cys)
c.3418A>T (p.Ser1140Cys)
c.3256A>T (p.Ser1086Cys)
c.3289A>T (p.Ser1097Cys)
3g.38576754T>CCA352138519SCN5Ac.3415A>G (p.Ser1139Gly)
c.3418A>G (p.Ser1140Gly)
c.3256A>G (p.Ser1086Gly)
c.3289A>G (p.Ser1097Gly)
3g.38576754T>GCA352138520SCN5Ac.3415A>C (p.Ser1139Arg)
c.3418A>C (p.Ser1140Arg)
c.3256A>C (p.Ser1086Arg)
c.3289A>C (p.Ser1097Arg)
3g.38576755G>ACA433134209SCN5Ac.3414C>T (p.Gly1138=)
c.3417C>T (p.Gly1139=)
c.3255C>T (p.Gly1085=)
c.3288C>T (p.Gly1096=)
 gnomAD v4
3g.38576755G>CCA433134210SCN5Ac.3414C>G (p.Gly1138=)
c.3417C>G (p.Gly1139=)
c.3255C>G (p.Gly1085=)
c.3288C>G (p.Gly1096=)
3g.38576755G>TCA433134211SCN5Ac.3414C>A (p.Gly1138=)
c.3417C>A (p.Gly1139=)
c.3255C>A (p.Gly1085=)
c.3288C>A (p.Gly1096=)
 gnomAD v4
3g.38576756C>ACA352138521SCN5Ac.3413G>T (p.Gly1138Val)
c.3416G>T (p.Gly1139Val)
c.3254G>T (p.Gly1085Val)
c.3287G>T (p.Gly1096Val)
 gnomAD v4
3g.38576756C=CA1358573186SCN5Ac.3413G= (p.Gly1138=)
c.3416G= (p.Gly1139=)
c.3254G= (p.Gly1085=)
c.3287G= (p.Gly1096=)
3g.38576756C>GCA352138522SCN5Ac.3413G>C (p.Gly1138Ala)
c.3416G>C (p.Gly1139Ala)
c.3254G>C (p.Gly1085Ala)
c.3287G>C (p.Gly1096Ala)
3g.38576756C>TCA72923981SCN5Ac.3413G>A (p.Gly1138Asp)
c.3416G>A (p.Gly1139Asp)
c.3254G>A (p.Gly1085Asp)
c.3287G>A (p.Gly1096Asp)
 ClinVar dbSNP
3g.38576757C>ACA352138523SCN5Ac.3412G>T (p.Gly1138Cys)
c.3415G>T (p.Gly1139Cys)
c.3253G>T (p.Gly1085Cys)
c.3286G>T (p.Gly1096Cys)
3g.38576757C>GCA352138524SCN5Ac.3412G>C (p.Gly1138Arg)
c.3415G>C (p.Gly1139Arg)
c.3253G>C (p.Gly1085Arg)
c.3286G>C (p.Gly1096Arg)
3g.38576757C>TCA352138525SCN5Ac.3412G>A (p.Gly1138Ser)
c.3415G>A (p.Gly1139Ser)
c.3253G>A (p.Gly1085Ser)
c.3286G>A (p.Gly1096Ser)
 ClinVar
3g.38576758C>ACA352138527SCN5Ac.3411G>T (p.Glu1137Asp)
c.3414G>T (p.Glu1138Asp)
c.3252G>T (p.Glu1084Asp)
c.3285G>T (p.Glu1095Asp)
 dbSNP
3g.38576758C=CA1358573187SCN5Ac.3411G= (p.Glu1137=)
c.3414G= (p.Glu1138=)
c.3252G= (p.Glu1084=)
c.3285G= (p.Glu1095=)
3g.38576758C>GCA352138526SCN5Ac.3411G>C (p.Glu1137Asp)
c.3414G>C (p.Glu1138Asp)
c.3252G>C (p.Glu1084Asp)
c.3285G>C (p.Glu1095Asp)
3g.38576758C>TCA72923984SCN5Ac.3411G>A (p.Glu1137=)
c.3414G>A (p.Glu1138=)
c.3252G>A (p.Glu1084=)
c.3285G>A (p.Glu1095=)
 ClinVar dbSNP
3g.38576759T>ACA352138528SCN5Ac.3410A>T (p.Glu1137Val)
c.3413A>T (p.Glu1138Val)
c.3251A>T (p.Glu1084Val)
c.3284A>T (p.Glu1095Val)
3g.38576759T>CCA352138529SCN5Ac.3410A>G (p.Glu1137Gly)
c.3413A>G (p.Glu1138Gly)
c.3251A>G (p.Glu1084Gly)
c.3284A>G (p.Glu1095Gly)
3g.38576759T>GCA017144SCN5Ac.3410A>C (p.Glu1137Ala)
c.3413A>C (p.Glu1138Ala)
c.3251A>C (p.Glu1084Ala)
c.3284A>C (p.Glu1095Ala)
 ClinVar dbSNP gnomAD v3 gnomAD v4
3g.38576759T=CA1358573188SCN5Ac.3410A= (p.Glu1137=)
c.3413A= (p.Glu1138=)
c.3251A= (p.Glu1084=)
c.3284A= (p.Glu1095=)
3g.38576760C>ACA352138530SCN5Ac.3409G>T (p.Glu1137Ter)
c.3412G>T (p.Glu1138Ter)
c.3250G>T (p.Glu1084Ter)
c.3283G>T (p.Glu1095Ter)
 dbSNP
3g.38576760C=CA1358573189SCN5Ac.3409G= (p.Glu1137=)
c.3412G= (p.Glu1138=)
c.3250G= (p.Glu1084=)
c.3283G= (p.Glu1095=)
3g.38576760C>GCA352138531SCN5Ac.3409G>C (p.Glu1137Gln)
c.3412G>C (p.Glu1138Gln)
c.3250G>C (p.Glu1084Gln)
c.3283G>C (p.Glu1095Gln)
3g.38576760C>TCA061821SCN5Ac.3409G>A (p.Glu1137Lys)
c.3412G>A (p.Glu1138Lys)
c.3250G>A (p.Glu1084Lys)
c.3283G>A (p.Glu1095Lys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.38576761G>ACA017137SCN5Ac.3408C>T (p.Ser1136=)
c.3411C>T (p.Ser1137=)
c.3249C>T (p.Ser1083=)
c.3282C>T (p.Ser1094=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38576761G>CCA433134215SCN5Ac.3408C>G (p.Ser1136=)
c.3411C>G (p.Ser1137=)
c.3249C>G (p.Ser1083=)
c.3282C>G (p.Ser1094=)
3g.38576761G=CA1358573190SCN5Ac.3408C= (p.Ser1136=)
c.3411C= (p.Ser1137=)
c.3249C= (p.Ser1083=)
c.3282C= (p.Ser1094=)
3g.38576761G>TCA433134216SCN5Ac.3408C>A (p.Ser1136=)
c.3411C>A (p.Ser1137=)
c.3249C>A (p.Ser1083=)
c.3282C>A (p.Ser1094=)
3g.38576762G>ACA352138532SCN5Ac.3407C>T (p.Ser1136Phe)
c.3410C>T (p.Ser1137Phe)
c.3248C>T (p.Ser1083Phe)
c.3281C>T (p.Ser1094Phe)
3g.38576762G>CCA352138533SCN5Ac.3407C>G (p.Ser1136Cys)
c.3410C>G (p.Ser1137Cys)
c.3248C>G (p.Ser1083Cys)
c.3281C>G (p.Ser1094Cys)
 gnomAD v4
3g.38576762G>TCA352138534SCN5Ac.3407C>A (p.Ser1136Tyr)
c.3410C>A (p.Ser1137Tyr)
c.3248C>A (p.Ser1083Tyr)
c.3281C>A (p.Ser1094Tyr)
3g.38576763A>CCA352138535SCN5Ac.3406T>G (p.Ser1136Ala)
c.3409T>G (p.Ser1137Ala)
c.3247T>G (p.Ser1083Ala)
c.3280T>G (p.Ser1094Ala)
3g.38576763A>GCA352138536SCN5Ac.3406T>C (p.Ser1136Pro)
c.3409T>C (p.Ser1137Pro)
c.3247T>C (p.Ser1083Pro)
c.3280T>C (p.Ser1094Pro)
3g.38576763A>TCA352138537SCN5Ac.3406T>A (p.Ser1136Thr)
c.3409T>A (p.Ser1137Thr)
c.3247T>A (p.Ser1083Thr)
c.3280T>A (p.Ser1094Thr)
3g.38576764G>ACA433134217SCN5Ac.3405C>T (p.Cys1135=)
c.3408C>T (p.Cys1136=)
c.3246C>T (p.Cys1082=)
c.3279C>T (p.Cys1093=)
 gnomAD v4
3g.38576764G>CCA352138538SCN5Ac.3405C>G (p.Cys1135Trp)
c.3408C>G (p.Cys1136Trp)
c.3246C>G (p.Cys1082Trp)
c.3279C>G (p.Cys1093Trp)
3g.38576764G=CA1358573191SCN5Ac.3405C= (p.Cys1135=)
c.3408C= (p.Cys1136=)
c.3246C= (p.Cys1082=)
c.3279C= (p.Cys1093=)
3g.38576764G>TCA352138539SCN5Ac.3405C>A (p.Cys1135Ter)
c.3408C>A (p.Cys1136Ter)
c.3246C>A (p.Cys1082Ter)
c.3279C>A (p.Cys1093Ter)
 dbSNP
3g.38576765C>ACA352138540SCN5Ac.3404G>T (p.Cys1135Phe)
c.3407G>T (p.Cys1136Phe)
c.3245G>T (p.Cys1082Phe)
c.3278G>T (p.Cys1093Phe)
3g.38576765C=CA1358573192SCN5Ac.3404G= (p.Cys1135=)
c.3407G= (p.Cys1136=)
c.3245G= (p.Cys1082=)
c.3278G= (p.Cys1093=)
3g.38576765C>GCA352138541SCN5Ac.3404G>C (p.Cys1135Ser)
c.3407G>C (p.Cys1136Ser)
c.3245G>C (p.Cys1082Ser)
c.3278G>C (p.Cys1093Ser)
3g.38576765C>TCA352138542SCN5Ac.3404G>A (p.Cys1135Tyr)
c.3407G>A (p.Cys1136Tyr)
c.3245G>A (p.Cys1082Tyr)
c.3278G>A (p.Cys1093Tyr)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.38576766A>CCA352138543SCN5Ac.3403T>G (p.Cys1135Gly)
c.3406T>G (p.Cys1136Gly)
c.3244T>G (p.Cys1082Gly)
c.3277T>G (p.Cys1093Gly)
3g.38576766A>GCA352138544SCN5Ac.3403T>C (p.Cys1135Arg)
c.3406T>C (p.Cys1136Arg)
c.3244T>C (p.Cys1082Arg)
c.3277T>C (p.Cys1093Arg)
3g.38576766A>TCA352138545SCN5Ac.3403T>A (p.Cys1135Ser)
c.3406T>A (p.Cys1136Ser)
c.3244T>A (p.Cys1082Ser)
c.3277T>A (p.Cys1093Ser)
3g.38576767A>CCA352138546SCN5Ac.3402T>G (p.Ser1134Arg)
c.3405T>G (p.Ser1135Arg)
c.3243T>G (p.Ser1081Arg)
c.3276T>G (p.Ser1092Arg)
3g.38576767A>GCA433134218SCN5Ac.3402T>C (p.Ser1134=)
c.3405T>C (p.Ser1135=)
c.3243T>C (p.Ser1081=)
c.3276T>C (p.Ser1092=)
 gnomAD v4
3g.38576767A>TCA352138547SCN5Ac.3402T>A (p.Ser1134Arg)
c.3405T>A (p.Ser1135Arg)
c.3243T>A (p.Ser1081Arg)
c.3276T>A (p.Ser1092Arg)
3g.38576768C>ACA017130SCN5Ac.3401G>T (p.Ser1134Ile)
c.3404G>T (p.Ser1135Ile)
c.3242G>T (p.Ser1081Ile)
c.3275G>T (p.Ser1092Ile)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38576768C=CA1358573193SCN5Ac.3401G= (p.Ser1134=)
c.3404G= (p.Ser1135=)
c.3242G= (p.Ser1081=)
c.3275G= (p.Ser1092=)
3g.38576768C>GCA352138548SCN5Ac.3401G>C (p.Ser1134Thr)
c.3404G>C (p.Ser1135Thr)
c.3242G>C (p.Ser1081Thr)
c.3275G>C (p.Ser1092Thr)
 ClinVar dbSNP
3g.38576768C>TCA352138549SCN5Ac.3401G>A (p.Ser1134Asn)
c.3404G>A (p.Ser1135Asn)
c.3242G>A (p.Ser1081Asn)
c.3275G>A (p.Ser1092Asn)
 ClinVar
3g.38576769T>ACA352138552SCN5Ac.3400A>T (p.Ser1134Cys)
c.3403A>T (p.Ser1135Cys)
c.3241A>T (p.Ser1081Cys)
c.3274A>T (p.Ser1092Cys)
3g.38576769T>CCA352138551SCN5Ac.3400A>G (p.Ser1134Gly)
c.3403A>G (p.Ser1135Gly)
c.3241A>G (p.Ser1081Gly)
c.3274A>G (p.Ser1092Gly)
3g.38576769T>GCA352138550SCN5Ac.3400A>C (p.Ser1134Arg)
c.3403A>C (p.Ser1135Arg)
c.3241A>C (p.Ser1081Arg)
c.3274A>C (p.Ser1092Arg)
3g.38576770G>ACA433134219SCN5Ac.3399C>T (p.Asp1133=)
c.3402C>T (p.Asp1134=)
c.3240C>T (p.Asp1080=)
c.3273C>T (p.Asp1091=)
 gnomAD v4
3g.38576770G>CCA352138553SCN5Ac.3399C>G (p.Asp1133Glu)
c.3402C>G (p.Asp1134Glu)
c.3240C>G (p.Asp1080Glu)
c.3273C>G (p.Asp1091Glu)
 ClinVar dbSNP gnomAD v2 gnomAD v4
3g.38576770G=CA1358573194SCN5Ac.3399C= (p.Asp1133=)
c.3402C= (p.Asp1134=)
c.3240C= (p.Asp1080=)
c.3273C= (p.Asp1091=)
3g.38576770G>TCA352138554SCN5Ac.3399C>A (p.Asp1133Glu)
c.3402C>A (p.Asp1134Glu)
c.3240C>A (p.Asp1080Glu)
c.3273C>A (p.Asp1091Glu)
3g.38576771T>ACA352138555SCN5Ac.3398A>T (p.Asp1133Val)
c.3401A>T (p.Asp1134Val)
c.3239A>T (p.Asp1080Val)
c.3272A>T (p.Asp1091Val)
3g.38576771T>CCA352138556SCN5Ac.3398A>G (p.Asp1133Gly)
c.3401A>G (p.Asp1134Gly)
c.3239A>G (p.Asp1080Gly)
c.3272A>G (p.Asp1091Gly)
3g.38576771T>GCA352138557SCN5Ac.3398A>C (p.Asp1133Ala)
c.3401A>C (p.Asp1134Ala)
c.3239A>C (p.Asp1080Ala)
c.3272A>C (p.Asp1091Ala)
3g.38576772C>ACA352138558SCN5Ac.3397G>T (p.Asp1133Tyr)
c.3400G>T (p.Asp1134Tyr)
c.3238G>T (p.Asp1080Tyr)
c.3271G>T (p.Asp1091Tyr)
3g.38576772C=CA1358573195SCN5Ac.3397G= (p.Asp1133=)
c.3400G= (p.Asp1134=)
c.3238G= (p.Asp1080=)
c.3271G= (p.Asp1091=)
3g.38576772C>GCA352138559SCN5Ac.3397G>C (p.Asp1133His)
c.3400G>C (p.Asp1134His)
c.3238G>C (p.Asp1080His)
c.3271G>C (p.Asp1091His)
3g.38576772C>TCA061807SCN5Ac.3397G>A (p.Asp1133Asn)
c.3400G>A (p.Asp1134Asn)
c.3238G>A (p.Asp1080Asn)
c.3271G>A (p.Asp1091Asn)
 dbSNP ExAC gnomAD v2 COSMIC COSMIC COSMIC
3g.38576773C>ACA352138560SCN5Ac.3396G>T (p.Glu1132Asp)
c.3399G>T (p.Glu1133Asp)
c.3237G>T (p.Glu1079Asp)
c.3270G>T (p.Glu1090Asp)
3g.38576773C>GCA352138561SCN5Ac.3396G>C (p.Glu1132Asp)
c.3399G>C (p.Glu1133Asp)
c.3237G>C (p.Glu1079Asp)
c.3270G>C (p.Glu1090Asp)
3g.38576773C>TCA433134220SCN5Ac.3396G>A (p.Glu1132=)
c.3399G>A (p.Glu1133=)
c.3237G>A (p.Glu1079=)
c.3270G>A (p.Glu1090=)
 ClinVar
3g.38576774T>ACA352138562SCN5Ac.3395A>T (p.Glu1132Val)
c.3398A>T (p.Glu1133Val)
c.3236A>T (p.Glu1079Val)
c.3269A>T (p.Glu1090Val)
3g.38576774T>CCA352138563SCN5Ac.3395A>G (p.Glu1132Gly)
c.3398A>G (p.Glu1133Gly)
c.3236A>G (p.Glu1079Gly)
c.3269A>G (p.Glu1090Gly)
 gnomAD v4
3g.38576774T>GCA352138564SCN5Ac.3395A>C (p.Glu1132Ala)
c.3398A>C (p.Glu1133Ala)
c.3236A>C (p.Glu1079Ala)
c.3269A>C (p.Glu1090Ala)
3g.38576775C>ACA352138566SCN5Ac.3394G>T (p.Glu1132Ter)
c.3397G>T (p.Glu1133Ter)
c.3235G>T (p.Glu1079Ter)
c.3268G>T (p.Glu1090Ter)
 ClinVar dbSNP
3g.38576775C=CA1358573196SCN5Ac.3394G= (p.Glu1132=)
c.3397G= (p.Glu1133=)
c.3235G= (p.Glu1079=)
c.3268G= (p.Glu1090=)
3g.38576775C>GCA352138567SCN5Ac.3394G>C (p.Glu1132Gln)
c.3397G>C (p.Glu1133Gln)
c.3235G>C (p.Glu1079Gln)
c.3268G>C (p.Glu1090Gln)
3g.38576775C>TCA352138565SCN5Ac.3394G>A (p.Glu1132Lys)
c.3397G>A (p.Glu1133Lys)
c.3235G>A (p.Glu1079Lys)
c.3268G>A (p.Glu1090Lys)
 ClinVar dbSNP
3g.38576776T>ACA433134221SCN5Ac.3393A>T (p.Pro1131=)
c.3396A>T (p.Pro1132=)
c.3234A>T (p.Pro1078=)
c.3267A>T (p.Pro1089=)
 ClinVar dbSNP gnomAD v4
3g.38576776T>CCA061799SCN5Ac.3393A>G (p.Pro1131=)
c.3396A>G (p.Pro1132=)
c.3234A>G (p.Pro1078=)
c.3267A>G (p.Pro1089=)
 dbSNP ExAC gnomAD v2
3g.38576776T>GCA433134222SCN5Ac.3393A>C (p.Pro1131=)
c.3396A>C (p.Pro1132=)
c.3234A>C (p.Pro1078=)
c.3267A>C (p.Pro1089=)
3g.38576776T=CA1358573197SCN5Ac.3393A= (p.Pro1131=)
c.3396A= (p.Pro1132=)
c.3234A= (p.Pro1078=)
c.3267A= (p.Pro1089=)
3g.38576777G>ACA352138568SCN5Ac.3392C>T (p.Pro1131Leu)
c.3395C>T (p.Pro1132Leu)
c.3233C>T (p.Pro1078Leu)
c.3266C>T (p.Pro1089Leu)
 gnomAD v4 COSMIC COSMIC COSMIC
3g.38576777G>CCA352138570SCN5Ac.3392C>G (p.Pro1131Arg)
c.3395C>G (p.Pro1132Arg)
c.3233C>G (p.Pro1078Arg)
c.3266C>G (p.Pro1089Arg)
 ClinVar
3g.38576777G=CA1358573198SCN5Ac.3392C= (p.Pro1131=)
c.3395C= (p.Pro1132=)
c.3233C= (p.Pro1078=)
c.3266C= (p.Pro1089=)
3g.38576777G>TCA352138569SCN5Ac.3392C>A (p.Pro1131Gln)
c.3395C>A (p.Pro1132Gln)
c.3233C>A (p.Pro1078Gln)
c.3266C>A (p.Pro1089Gln)
 ClinVar dbSNP gnomAD v4
3g.38576778G>ACA017122SCN5Ac.3391C>T (p.Pro1131Ser)
c.3394C>T (p.Pro1132Ser)
c.3232C>T (p.Pro1078Ser)
c.3265C>T (p.Pro1089Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38576778G>CCA352138571SCN5Ac.3391C>G (p.Pro1131Ala)
c.3394C>G (p.Pro1132Ala)
c.3232C>G (p.Pro1078Ala)
c.3265C>G (p.Pro1089Ala)
 ClinVar
3g.38576778G=CA1358573199SCN5Ac.3391C= (p.Pro1131=)
c.3394C= (p.Pro1132=)
c.3232C= (p.Pro1078=)
c.3265C= (p.Pro1089=)
3g.38576778G>TCA352138572SCN5Ac.3391C>A (p.Pro1131Thr)
c.3394C>A (p.Pro1132Thr)
c.3232C>A (p.Pro1078Thr)
c.3265C>A (p.Pro1089Thr)
3g.38576779G>ACA061789SCN5Ac.3390C>T (p.Thr1130=)
c.3393C>T (p.Thr1131=)
c.3231C>T (p.Thr1077=)
c.3264C>T (p.Thr1088=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC
3g.38576779G>CCA433134223SCN5Ac.3390C>G (p.Thr1130=)
c.3393C>G (p.Thr1131=)
c.3231C>G (p.Thr1077=)
c.3264C>G (p.Thr1088=)
3g.38576779G=CA1358573200SCN5Ac.3390C= (p.Thr1130=)
c.3393C= (p.Thr1131=)
c.3231C= (p.Thr1077=)
c.3264C= (p.Thr1088=)
3g.38576779G>TCA433134224SCN5Ac.3390C>A (p.Thr1130=)
c.3393C>A (p.Thr1131=)
c.3231C>A (p.Thr1077=)
c.3264C>A (p.Thr1088=)
3g.38576780G>ACA017114SCN5Ac.3389C>T (p.Thr1130Ile)
c.3392C>T (p.Thr1131Ile)
c.3230C>T (p.Thr1077Ile)
c.3263C>T (p.Thr1088Ile)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38576780G>CCA352138573SCN5Ac.3389C>G (p.Thr1130Ser)
c.3392C>G (p.Thr1131Ser)
c.3230C>G (p.Thr1077Ser)
c.3263C>G (p.Thr1088Ser)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.38576780G=CA1358573201SCN5Ac.3389C= (p.Thr1130=)
c.3392C= (p.Thr1131=)
c.3230C= (p.Thr1077=)
c.3263C= (p.Thr1088=)
3g.38576780G>TCA352138574SCN5Ac.3389C>A (p.Thr1130Asn)
c.3392C>A (p.Thr1131Asn)
c.3230C>A (p.Thr1077Asn)
c.3263C>A (p.Thr1088Asn)
 dbSNP gnomAD v2 gnomAD v4
3g.38576781T>ACA061773SCN5Ac.3388A>T (p.Thr1130Ser)
c.3391A>T (p.Thr1131Ser)
c.3229A>T (p.Thr1077Ser)
c.3262A>T (p.Thr1088Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38576781T>CCA352138575SCN5Ac.3388A>G (p.Thr1130Ala)
c.3391A>G (p.Thr1131Ala)
c.3229A>G (p.Thr1077Ala)
c.3262A>G (p.Thr1088Ala)
3g.38576781T>GCA352138576SCN5Ac.3388A>C (p.Thr1130Pro)
c.3391A>C (p.Thr1131Pro)
c.3229A>C (p.Thr1077Pro)
c.3262A>C (p.Thr1088Pro)
 ClinVar dbSNP
3g.38576781T=CA1358573202SCN5Ac.3388A= (p.Thr1130=)
c.3391A= (p.Thr1131=)
c.3229A= (p.Thr1077=)
c.3262A= (p.Thr1088=)
3g.38576782C>ACA352138577SCN5Ac.3388-1G>T (n.3388-1G>T)
c.3391-1G>T (n.3391-1G>T)
c.3229-1G>T (n.3229-1G>T)
c.3262-1G>T (n.3262-1G>T)
 gnomAD v4
3g.38576782C>GCA352138578SCN5Ac.3388-1G>C (n.3388-1G>C)
c.3391-1G>C (n.3391-1G>C)
c.3229-1G>C (n.3229-1G>C)
c.3262-1G>C (n.3262-1G>C)
 ClinVar
3g.38576782C>TCA352138579SCN5Ac.3388-1G>A (n.3388-1G>A)
c.3391-1G>A (n.3391-1G>A)
c.3229-1G>A (n.3229-1G>A)
c.3262-1G>A (n.3262-1G>A)
 ClinVar dbSNP
3g.38576783T>ACA352138580SCN5Ac.3388-2A>T (n.3388-2A>T)
c.3391-2A>T (n.3391-2A>T)
c.3229-2A>T (n.3229-2A>T)
c.3262-2A>T (n.3262-2A>T)
3g.38576783T>CCA352138582SCN5Ac.3388-2A>G (n.3388-2A>G)
c.3391-2A>G (n.3391-2A>G)
c.3229-2A>G (n.3229-2A>G)
c.3262-2A>G (n.3262-2A>G)
3g.38576783T>GCA352138581SCN5Ac.3388-2A>C (n.3388-2A>C)
c.3391-2A>C (n.3391-2A>C)
c.3229-2A>C (n.3229-2A>C)
c.3262-2A>C (n.3262-2A>C)
3g.38576784A=CA1358573203SCN5Ac.3388-3T= (n.3388-3T=)
c.3391-3T= (n.3391-3T=)
c.3229-3T= (n.3229-3T=)
c.3262-3T= (n.3262-3T=)
3g.38576784A>GCA16604913SCN5Ac.3388-3T>C (n.3388-3T>C)
c.3391-3T>C (n.3391-3T>C)
c.3229-3T>C (n.3229-3T>C)
c.3262-3T>C (n.3262-3T>C)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.38576785T>CCA542272680SCN5Ac.3388-4A>G (n.3388-4A>G)
c.3391-4A>G (n.3391-4A>G)
c.3229-4A>G (n.3229-4A>G)
c.3262-4A>G (n.3262-4A>G)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.38576785T=CA1358573204SCN5Ac.3388-4A= (n.3388-4A=)
c.3391-4A= (n.3391-4A=)
c.3229-4A= (n.3229-4A=)
c.3262-4A= (n.3262-4A=)
3g.38576786G>ACA542272682SCN5Ac.3388-5C>T (n.3388-5C>T)
c.3391-5C>T (n.3391-5C>T)
c.3229-5C>T (n.3229-5C>T)
c.3262-5C>T (n.3262-5C>T)
 ClinVar dbSNP gnomAD v2 gnomAD v4
3g.38576786G=CA1358573205SCN5Ac.3388-5C= (n.3388-5C=)
c.3391-5C= (n.3391-5C=)
c.3229-5C= (n.3229-5C=)
c.3262-5C= (n.3262-5C=)
3g.38576786G>TCA2665112491SCN5Ac.3388-5C>A (n.3388-5C>A)
c.3391-5C>A (n.3391-5C>A)
c.3229-5C>A (n.3229-5C>A)
c.3262-5C>A (n.3262-5C>A)
 gnomAD v4

Number of alleles fetched