Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.38581004_38581017delinsGCCACAGCGATGGGCA1358576272SCN5Ac.3142_3155delinsCCCATCGCTGTGGC (p.Pro1048=)
c.3013_3026delinsCCCATCGCTGTGGC (p.Pro1005=)
3g.38581006delCA2499216750SCN5Ac.3154del (p.Ala1052ProfsTer?)
c.3025del (p.Ala1009ProfsTer?)
ClinVar dbSNP
3g.38581005_38581017delinsACACAGTCAGACA10582194SCN5Ac.3142_3154delinsTCTGACTGTGT (p.Pro1048SerfsTer10)
c.3013_3025delinsTCTGACTGTGT (p.Pro1005SerfsTer10)
ClinVar dbSNP
3g.38581005_38581017delinsCCACAGCGATGGGCA1358576285SCN5Ac.3142_3154delinsCCCATCGCTGTGG (p.Pro1048=)
c.3013_3025delinsCCCATCGCTGTGG (p.Pro1005=)
3g.38581006C>ACA433135140SCN5Ac.3153G>T (p.Val1051=)
c.3024G>T (p.Val1008=)
dbSNP
3g.38581006C>GCA433135142SCN5Ac.3153G>C (p.Val1051=)
c.3024G>C (p.Val1008=)
3g.38581006C>TCA433135144SCN5Ac.3153G>A (p.Val1051=)
c.3024G>A (p.Val1008=)
3g.38581006_38581017delinsACACAGTCAGACA016864SCN5Ac.3142_3153delinsTCTGACTGTGT (p.Pro1048SerfsTer?)
c.3013_3024delinsTCTGACTGTGT (p.Pro1005SerfsTer?)
ClinVar dbSNP
3g.38581007A=CA1358576294SCN5Ac.3152T= (p.Val1051=)
c.3023T= (p.Val1008=)
3g.38581007A>CCA352139267SCN5Ac.3152T>G (p.Val1051Gly)
c.3023T>G (p.Val1008Gly)
3g.38581007A>GCA061317SCN5Ac.3152T>C (p.Val1051Ala)
c.3023T>C (p.Val1008Ala)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.38581007A>TCA352139270SCN5Ac.3152T>A (p.Val1051Glu)
c.3023T>A (p.Val1008Glu)
3g.38581008C>ACA352139272SCN5Ac.3151G>T (p.Val1051Leu)
c.3022G>T (p.Val1008Leu)
3g.38581008C>GCA352139274SCN5Ac.3151G>C (p.Val1051Leu)
c.3022G>C (p.Val1008Leu)
3g.38581008C>TCA352139275SCN5Ac.3151G>A (p.Val1051Met)
c.3022G>A (p.Val1008Met)
3g.38581009A>CCA433135159SCN5Ac.3150T>G (p.Ala1050=)
c.3021T>G (p.Ala1007=)
3g.38581009A>GCA433135157SCN5Ac.3150T>C (p.Ala1050=)
c.3021T>C (p.Ala1007=)
3g.38581009A>TCA433135156SCN5Ac.3150T>A (p.Ala1050=)
c.3021T>A (p.Ala1007=)
3g.38581010G>ACA352139278SCN5Ac.3149C>T (p.Ala1050Val)
c.3020C>T (p.Ala1007Val)
3g.38581010G>CCA352139279SCN5Ac.3149C>G (p.Ala1050Gly)
c.3020C>G (p.Ala1007Gly)
3g.38581010G=CA1358576297SCN5Ac.3149C= (p.Ala1050=)
c.3020C= (p.Ala1007=)
3g.38581010G>TCA352139281SCN5Ac.3149C>A (p.Ala1050Asp)
c.3020C>A (p.Ala1007Asp)
3g.38581010_38581011insTCA542615698SCN5Ac.3148_3149insA (p.Ala1050AspfsTer9)
c.3019_3020insA (p.Ala1007AspfsTer9)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.38581011C>ACA352139282SCN5Ac.3148G>T (p.Ala1050Ser)
c.3019G>T (p.Ala1007Ser)
dbSNP gnomAD v2
3g.38581011C=CA1358576301SCN5Ac.3148G= (p.Ala1050=)
c.3019G= (p.Ala1007=)
3g.38581011C>GCA352139284SCN5Ac.3148G>C (p.Ala1050Pro)
c.3019G>C (p.Ala1007Pro)
3g.38581011C>TCA352139286SCN5Ac.3148G>A (p.Ala1050Thr)
c.3019G>A (p.Ala1007Thr)
ClinVar dbSNP gnomAD v2 gnomAD v4
3g.38581011_38581012insACA542615699SCN5Ac.3147_3148insT (p.Ala1050CysfsTer9)
c.3018_3019insT (p.Ala1007CysfsTer9)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.38581012G>ACA72926171SCN5Ac.3147C>T (p.Ile1049=)
c.3018C>T (p.Ile1006=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.38581012G>CCA352139289SCN5Ac.3147C>G (p.Ile1049Met)
c.3018C>G (p.Ile1006Met)
dbSNP
3g.38581012G=CA1358576306SCN5Ac.3147C= (p.Ile1049=)
c.3018C= (p.Ile1006=)
3g.38581012G>TCA433135167SCN5Ac.3147C>A (p.Ile1049=)
c.3018C>A (p.Ile1006=)
3g.38581013A>CCA352139291SCN5Ac.3146T>G (p.Ile1049Ser)
c.3017T>G (p.Ile1006Ser)
3g.38581013A>GCA352139294SCN5Ac.3146T>C (p.Ile1049Thr)
c.3017T>C (p.Ile1006Thr)
3g.38581013A>TCA352139292SCN5Ac.3146T>A (p.Ile1049Asn)
c.3017T>A (p.Ile1006Asn)
3g.38581013_38581015delinsATGCA1358576311SCN5Ac.3144_3146delinsCAT (p.Pro1048=)
c.3015_3017delinsCAT (p.Pro1005=)
3g.38581013_38581017delinsATGGGCA1358576310SCN5Ac.3142_3146delinsCCCAT (p.Pro1048=)
c.3013_3017delinsCCCAT (p.Pro1005=)
3g.38581014T>ACA352139297SCN5Ac.3145A>T (p.Ile1049Phe)
c.3016A>T (p.Ile1006Phe)
3g.38581014T>CCA352139300SCN5Ac.3145A>G (p.Ile1049Val)
c.3016A>G (p.Ile1006Val)
ClinVar dbSNP
3g.38581014T>GCA352139298SCN5Ac.3145A>C (p.Ile1049Leu)
c.3016A>C (p.Ile1006Leu)
3g.38581014_38581015delCA1358576316SCN5Ac.3144_3145del (p.Ile1049ArgfsTer9)
c.3015_3016del (p.Ile1006ArgfsTer9)
dbSNP
3g.38581014_38581017delCA542615700SCN5Ac.3142_3145del (p.Pro1048SerfsTer?)
c.3013_3016del (p.Pro1005SerfsTer?)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.38581015G>ACA433135176SCN5Ac.3144C>T (p.Pro1048=)
c.3015C>T (p.Pro1005=)
3g.38581015G>CCA433135178SCN5Ac.3144C>G (p.Pro1048=)
c.3015C>G (p.Pro1005=)
3g.38581015G>TCA433135181SCN5Ac.3144C>A (p.Pro1048=)
c.3015C>A (p.Pro1005=)
3g.38581016G>ACA352139302SCN5Ac.3143C>T (p.Pro1048Leu)
c.3014C>T (p.Pro1005Leu)
gnomAD v4
3g.38581016G>CCA352139303SCN5Ac.3143C>G (p.Pro1048Arg)
c.3014C>G (p.Pro1005Arg)
3g.38581016G>TCA352139305SCN5Ac.3143C>A (p.Pro1048His)
c.3014C>A (p.Pro1005His)
3g.38581017G>ACA352139308SCN5Ac.3142C>T (p.Pro1048Ser)
c.3013C>T (p.Pro1005Ser)
ClinVar dbSNP gnomAD v2 gnomAD v4
3g.38581017G>CCA352139309SCN5Ac.3142C>G (p.Pro1048Ala)
c.3013C>G (p.Pro1005Ala)

Number of alleles fetched