Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.38581070T>ACA352139534SCN5Ac.3089A>T (p.Glu1030Val)
c.2960A>T (p.Glu987Val)
3g.38581070T>CCA352139536SCN5Ac.3089A>G (p.Glu1030Gly)
c.2960A>G (p.Glu987Gly)
3g.38581070T>GCA352139538SCN5Ac.3089A>C (p.Glu1030Ala)
c.2960A>C (p.Glu987Ala)
3g.38581071C>ACA352139540SCN5Ac.3088G>T (p.Glu1030Ter)
c.2959G>T (p.Glu987Ter)
dbSNP
3g.38581071C=CA1358576460SCN5Ac.3088G= (p.Glu1030=)
c.2959G= (p.Glu987=)
3g.38581071C>GCA352139542SCN5Ac.3088G>C (p.Glu1030Gln)
c.2959G>C (p.Glu987Gln)
ClinVar dbSNP
3g.38581071C>TCA352139544SCN5Ac.3088G>A (p.Glu1030Lys)
c.2959G>A (p.Glu987Lys)
3g.38581072C>ACA352139546SCN5Ac.3087G>T (p.Glu1029Asp)
c.2958G>T (p.Glu986Asp)
3g.38581072C>GCA352139547SCN5Ac.3087G>C (p.Glu1029Asp)
c.2958G>C (p.Glu986Asp)
3g.38581072C>TCA433135360SCN5Ac.3087G>A (p.Glu1029=)
c.2958G>A (p.Glu986=)
ClinVar dbSNP
3g.38581073T>ACA352139553SCN5Ac.3086A>T (p.Glu1029Val)
c.2957A>T (p.Glu986Val)
3g.38581073T>CCA352139551SCN5Ac.3086A>G (p.Glu1029Gly)
c.2957A>G (p.Glu986Gly)
3g.38581073T>GCA352139550SCN5Ac.3086A>C (p.Glu1029Ala)
c.2957A>C (p.Glu986Ala)
3g.38581074C>ACA352139555SCN5Ac.3085G>T (p.Glu1029Ter)
c.2956G>T (p.Glu986Ter)
dbSNP
3g.38581074C=CA1358576465SCN5Ac.3085G= (p.Glu1029=)
c.2956G= (p.Glu986=)
3g.38581074C>GCA352139557SCN5Ac.3085G>C (p.Glu1029Gln)
c.2956G>C (p.Glu986Gln)
3g.38581074C>TCA16617949SCN5Ac.3085G>A (p.Glu1029Lys)
c.2956G>A (p.Glu986Lys)
ClinVar dbSNP gnomAD v2 gnomAD v4
3g.38581075A>CCA352139560SCN5Ac.3084T>G (p.Phe1028Leu)
c.2955T>G (p.Phe985Leu)
3g.38581075A>GCA433135367SCN5Ac.3084T>C (p.Phe1028=)
c.2955T>C (p.Phe985=)
3g.38581075A>TCA352139561SCN5Ac.3084T>A (p.Phe1028Leu)
c.2955T>A (p.Phe985Leu)
3g.38581076A>CCA352139563SCN5Ac.3083T>G (p.Phe1028Cys)
c.2954T>G (p.Phe985Cys)
gnomAD v4
3g.38581076A>GCA352139565SCN5Ac.3083T>C (p.Phe1028Ser)
c.2954T>C (p.Phe985Ser)
3g.38581076A>TCA352139567SCN5Ac.3083T>A (p.Phe1028Tyr)
c.2954T>A (p.Phe985Tyr)
3g.38581077A>CCA352139570SCN5Ac.3082T>G (p.Phe1028Val)
c.2953T>G (p.Phe985Val)
gnomAD v3 gnomAD v4
3g.38581077A>GCA352139571SCN5Ac.3082T>C (p.Phe1028Leu)
c.2953T>C (p.Phe985Leu)
3g.38581077A>TCA352139573SCN5Ac.3082T>A (p.Phe1028Ile)
c.2953T>A (p.Phe985Ile)
3g.38581077_38581078delinsACCA1358576469SCN5Ac.3081_3082delinsGT (p.Arg1027=)
c.2952_2953delinsGT (p.Arg984=)
3g.38581078C>ACA433135374SCN5Ac.3081G>T (p.Arg1027=)
c.2952G>T (p.Arg984=)
ClinVar dbSNP gnomAD v4
3g.38581078C=CA1358576474SCN5Ac.3081G= (p.Arg1027=)
c.2952G= (p.Arg984=)
3g.38581078C>GCA433135376SCN5Ac.3081G>C (p.Arg1027=)
c.2952G>C (p.Arg984=)
3g.38581078C>TCA72926234SCN5Ac.3081G>A (p.Arg1027=)
c.2952G>A (p.Arg984=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC
3g.38581079delCA658657284SCN5Ac.3081del (p.Phe1028LeufsTer?)
c.2952del (p.Phe985LeufsTer?)
ClinVar dbSNP
3g.38581079C>ACA352139577SCN5Ac.3080G>T (p.Arg1027Leu)
c.2951G>T (p.Arg984Leu)
gnomAD v4
3g.38581079C=CA1358576480SCN5Ac.3080G= (p.Arg1027=)
c.2951G= (p.Arg984=)
3g.38581079C>GCA72926239SCN5Ac.3080G>C (p.Arg1027Pro)
c.2951G>C (p.Arg984Pro)
dbSNP gnomAD v2 gnomAD v4
3g.38581079C>TCA061251SCN5Ac.3080G>A (p.Arg1027Gln)
c.2951G>A (p.Arg984Gln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.38581080G>ACA352139580SCN5Ac.3079C>T (p.Arg1027Trp)
c.2950C>T (p.Arg984Trp)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC
3g.38581080G>CCA352139582SCN5Ac.3079C>G (p.Arg1027Gly)
c.2950C>G (p.Arg984Gly)
3g.38581080G=CA1358576493SCN5Ac.3079C= (p.Arg1027=)
c.2950C= (p.Arg984=)
3g.38581080G>TCA433135384SCN5Ac.3079C>A (p.Arg1027=)
c.2950C>A (p.Arg984=)
dbSNP
3g.38581081T>ACA433135386SCN5Ac.3078A>T (p.Thr1026=)
c.2949A>T (p.Thr983=)
3g.38581081T>CCA061246SCN5Ac.3078A>G (p.Thr1026=)
c.2949A>G (p.Thr983=)
dbSNP ExAC gnomAD v2 gnomAD v4
3g.38581081T>GCA433135389SCN5Ac.3078A>C (p.Thr1026=)
c.2949A>C (p.Thr983=)
3g.38581081T=CA1358576501SCN5Ac.3078A= (p.Thr1026=)
c.2949A= (p.Thr983=)
3g.38581082G>ACA352139585SCN5Ac.3077C>T (p.Thr1026Ile)
c.2948C>T (p.Thr983Ile)
3g.38581082G>CCA352139588SCN5Ac.3077C>G (p.Thr1026Arg)
c.2948C>G (p.Thr983Arg)
3g.38581082G>TCA352139589SCN5Ac.3077C>A (p.Thr1026Lys)
c.2948C>A (p.Thr983Lys)
3g.38581083T>ACA352139596SCN5Ac.3076A>T (p.Thr1026Ser)
c.2947A>T (p.Thr983Ser)
3g.38581083T>CCA352139592SCN5Ac.3076A>G (p.Thr1026Ala)
c.2947A>G (p.Thr983Ala)
gnomAD v4
3g.38581083T>GCA352139594SCN5Ac.3076A>C (p.Thr1026Pro)
c.2947A>C (p.Thr983Pro)

Number of alleles fetched