Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.38580910_38580997delinsCATGCAGGGGTGAGGGCCCACCTGCTTGCTGGACTCCTCCTCCGTGCCCAGGCTGTTCTCCTCATCTTCTTCTTGGTCATCTGTGTCTCA1358576032SCN5Ac.3162_3228+21delinsAGACACAGATGACCAAGAAGAAGATGAGGAGAACAGCCTGGGCACGGAGGAGGAGTCCAGCAAGCAGGTGGGCCCTCACCCCTGCATG
c.3033_3099+21delinsAGACACAGATGACCAAGAAGAAGATGAGGAGAACAGCCTGGGCACGGAGGAGGAGTCCAGCAAGCAGGTGGGCCCTCACCCCTGCATG
3g.38580911_38580997delCA1047003605SCN5Ac.3162_3228+20del
c.3033_3099+20del
dbSNP gnomAD v3 gnomAD v4
3g.38580979T>ACA352139140SCN5Ac.3180A>T (p.Glu1060Asp)
c.3051A>T (p.Glu1017Asp)
3g.38580979T>CCA433135063SCN5Ac.3180A>G (p.Glu1060=)
c.3051A>G (p.Glu1017=)
3g.38580979T>GCA352139141SCN5Ac.3180A>C (p.Glu1060Asp)
c.3051A>C (p.Glu1017Asp)
3g.38580980T>ACA352139143SCN5Ac.3179A>T (p.Glu1060Val)
c.3050A>T (p.Glu1017Val)
3g.38580980T>CCA352139145SCN5Ac.3179A>G (p.Glu1060Gly)
c.3050A>G (p.Glu1017Gly)
3g.38580980T>GCA352139147SCN5Ac.3179A>C (p.Glu1060Ala)
c.3050A>C (p.Glu1017Ala)
3g.38580981C>ACA352139152SCN5Ac.3178G>T (p.Glu1060Ter)
c.3049G>T (p.Glu1017Ter)
dbSNP
3g.38580981C=CA1358576218SCN5Ac.3178G= (p.Glu1060=)
c.3049G= (p.Glu1017=)
3g.38580981C>GCA352139149SCN5Ac.3178G>C (p.Glu1060Gln)
c.3049G>C (p.Glu1017Gln)
3g.38580981C>TCA352139150SCN5Ac.3178G>A (p.Glu1060Lys)
c.3049G>A (p.Glu1017Lys)
COSMIC COSMIC COSMIC
3g.38580982T>ACA352139154SCN5Ac.3177A>T (p.Gln1059His)
c.3048A>T (p.Gln1016His)
3g.38580982T>CCA433135075SCN5Ac.3177A>G (p.Gln1059=)
c.3048A>G (p.Gln1016=)
3g.38580982T>GCA352139155SCN5Ac.3177A>C (p.Gln1059His)
c.3048A>C (p.Gln1016His)
3g.38580983T>ACA352139156SCN5Ac.3176A>T (p.Gln1059Leu)
c.3047A>T (p.Gln1016Leu)
3g.38580983T>CCA352139158SCN5Ac.3176A>G (p.Gln1059Arg)
c.3047A>G (p.Gln1016Arg)
3g.38580983T>GCA352139159SCN5Ac.3176A>C (p.Gln1059Pro)
c.3047A>C (p.Gln1016Pro)
3g.38580984G>ACA352139161SCN5Ac.3175C>T (p.Gln1059Ter)
c.3046C>T (p.Gln1016Ter)
ClinVar dbSNP
3g.38580984G>CCA352139163SCN5Ac.3175C>G (p.Gln1059Glu)
c.3046C>G (p.Gln1016Glu)
3g.38580984G>TCA352139165SCN5Ac.3175C>A (p.Gln1059Lys)
c.3046C>A (p.Gln1016Lys)
3g.38580985G>ACA433135079SCN5Ac.3174C>T (p.Asp1058=)
c.3045C>T (p.Asp1015=)
3g.38580985G>CCA352139167SCN5Ac.3174C>G (p.Asp1058Glu)
c.3045C>G (p.Asp1015Glu)
3g.38580985G>TCA352139168SCN5Ac.3174C>A (p.Asp1058Glu)
c.3045C>A (p.Asp1015Glu)
COSMIC COSMIC COSMIC
3g.38580986T>ACA352139171SCN5Ac.3173A>T (p.Asp1058Val)
c.3044A>T (p.Asp1015Val)
3g.38580986T>CCA352139172SCN5Ac.3173A>G (p.Asp1058Gly)
c.3044A>G (p.Asp1015Gly)
dbSNP
3g.38580986T>GCA72926107SCN5Ac.3173A>C (p.Asp1058Ala)
c.3044A>C (p.Asp1015Ala)
ClinVar dbSNP
3g.38580986T=CA1358576224SCN5Ac.3173A= (p.Asp1058=)
c.3044A= (p.Asp1015=)
3g.38580987C>ACA352139178SCN5Ac.3172G>T (p.Asp1058Tyr)
c.3043G>T (p.Asp1015Tyr)
gnomAD v4
3g.38580987C>GCA352139180SCN5Ac.3172G>C (p.Asp1058His)
c.3043G>C (p.Asp1015His)
3g.38580987C>TCA352139176SCN5Ac.3172G>A (p.Asp1058Asn)
c.3043G>A (p.Asp1015Asn)
3g.38580987_38580988delinsTCA2586972013SCN5Ac.3171_3172delinsA (p.Asp1057GlufsTer?)
c.3042_3043delinsA (p.Asp1014GlufsTer?)
3g.38580988A=CA1358576227SCN5Ac.3171T= (p.Asp1057=)
c.3042T= (p.Asp1014=)
3g.38580988A>CCA352139183SCN5Ac.3171T>G (p.Asp1057Glu)
c.3042T>G (p.Asp1014Glu)
3g.38580988A>GCA433135087SCN5Ac.3171T>C (p.Asp1057=)
c.3042T>C (p.Asp1014=)
dbSNP gnomAD v3 gnomAD v4
3g.38580988A>TCA352139185SCN5Ac.3171T>A (p.Asp1057Glu)
c.3042T>A (p.Asp1014Glu)
3g.38580989T>ACA352139186SCN5Ac.3170A>T (p.Asp1057Val)
c.3041A>T (p.Asp1014Val)
3g.38580989T>CCA352139187SCN5Ac.3170A>G (p.Asp1057Gly)
c.3041A>G (p.Asp1014Gly)
3g.38580989T>GCA352139190SCN5Ac.3170A>C (p.Asp1057Ala)
c.3041A>C (p.Asp1014Ala)
3g.38580993_38580998delCA2573052155SCN5Ac.3165_3170del (p.Thr1056_Asp1057del)
c.3036_3041del (p.Thr1013_Asp1014del)
ClinVar dbSNP
3g.38580990C>ACA352139192SCN5Ac.3169G>T (p.Asp1057Tyr)
c.3040G>T (p.Asp1014Tyr)
3g.38580990C=CA1358576232SCN5Ac.3169G= (p.Asp1057=)
c.3040G= (p.Asp1014=)
3g.38580990C>GCA352139194SCN5Ac.3169G>C (p.Asp1057His)
c.3040G>C (p.Asp1014His)
3g.38580990C>TCA352139195SCN5Ac.3169G>A (p.Asp1057Asn)
c.3040G>A (p.Asp1014Asn)
ClinVar dbSNP gnomAD v3 gnomAD v4
3g.38580991T>ACA433135093SCN5Ac.3168A>T (p.Thr1056=)
c.3039A>T (p.Thr1013=)
3g.38580991T>CCA433135094SCN5Ac.3168A>G (p.Thr1056=)
c.3039A>G (p.Thr1013=)
dbSNP
3g.38580991T>GCA061330SCN5Ac.3168A>C (p.Thr1056=)
c.3039A>C (p.Thr1013=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38580991T=CA1358576237SCN5Ac.3168A= (p.Thr1056=)
c.3039A= (p.Thr1013=)
3g.38580992G>ACA352139199SCN5Ac.3167C>T (p.Thr1056Ile)
c.3038C>T (p.Thr1013Ile)
3g.38580992G>CCA352139201SCN5Ac.3167C>G (p.Thr1056Arg)
c.3038C>G (p.Thr1013Arg)

Number of alleles fetched