Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.38585746C>ACA352141485SCN5Ac.2732G>T (p.Gly911Val)
c.2603G>T (p.Gly868Val)
3g.38585746C=CA1358577404SCN5Ac.2732G= (p.Gly911=)
c.2603G= (p.Gly868=)
3g.38585746C>GCA352141488SCN5Ac.2732G>C (p.Gly911Ala)
c.2603G>C (p.Gly868Ala)
3g.38585746C>TCA352141486SCN5Ac.2732G>A (p.Gly911Glu)
c.2603G>A (p.Gly868Glu)
dbSNP gnomAD v2 gnomAD v4
3g.38585747C>ACA352141490SCN5Ac.2731G>T (p.Gly911Trp)
c.2602G>T (p.Gly868Trp)
gnomAD v4
3g.38585747C>GCA352141493SCN5Ac.2731G>C (p.Gly911Arg)
c.2602G>C (p.Gly868Arg)
3g.38585747C>TCA352141492SCN5Ac.2731G>A (p.Gly911Arg)
c.2602G>A (p.Gly868Arg)
gnomAD v4
3g.38585748C>ACA433332654SCN5Ac.2730G>T (p.Ser910=)
c.2601G>T (p.Ser867=)
3g.38585748C=CA1358577405SCN5Ac.2730G= (p.Ser910=)
c.2601G= (p.Ser867=)
3g.38585748C>GCA433332655SCN5Ac.2730G>C (p.Ser910=)
c.2601G>C (p.Ser867=)
dbSNP gnomAD v2
3g.38585748C>TCA060753SCN5Ac.2730G>A (p.Ser910=)
c.2601G>A (p.Ser867=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC
3g.38585749G>ACA016445SCN5Ac.2729C>T (p.Ser910Leu)
c.2600C>T (p.Ser867Leu)
ClinVar dbSNP gnomAD v2 gnomAD v4
3g.38585749G>CCA352141495SCN5Ac.2729C>G (p.Ser910Trp)
c.2600C>G (p.Ser867Trp)
3g.38585749G=CA1358577406SCN5Ac.2729C= (p.Ser910=)
c.2600C= (p.Ser867=)
3g.38585749G>TCA352141497SCN5Ac.2729C>A (p.Ser910Ter)
c.2600C>A (p.Ser867Ter)
dbSNP
3g.38585750A>CCA352141499SCN5Ac.2728T>G (p.Ser910Ala)
c.2599T>G (p.Ser867Ala)
3g.38585750A>GCA352141500SCN5Ac.2728T>C (p.Ser910Pro)
c.2599T>C (p.Ser867Pro)
3g.38585750A>TCA352141502SCN5Ac.2728T>A (p.Ser910Thr)
c.2599T>A (p.Ser867Thr)
3g.38585751C>ACA433332659SCN5Ac.2727G>T (p.Val909=)
c.2598G>T (p.Val866=)
3g.38585751C>GCA433332661SCN5Ac.2727G>C (p.Val909=)
c.2598G>C (p.Val866=)
3g.38585751C>TCA433332662SCN5Ac.2727G>A (p.Val909=)
c.2598G>A (p.Val866=)
3g.38585752A=CA1358577407SCN5Ac.2726T= (p.Val909=)
c.2597T= (p.Val866=)
3g.38585752A>CCA352141503SCN5Ac.2726T>G (p.Val909Gly)
c.2597T>G (p.Val866Gly)
dbSNP
3g.38585752A>GCA352141505SCN5Ac.2726T>C (p.Val909Ala)
c.2597T>C (p.Val866Ala)
3g.38585752A>TCA352141506SCN5Ac.2726T>A (p.Val909Glu)
c.2597T>A (p.Val866Glu)
3g.38585753C>ACA352141508SCN5Ac.2725G>T (p.Val909Leu)
c.2596G>T (p.Val866Leu)
dbSNP
3g.38585753C=CA1358577408SCN5Ac.2725G= (p.Val909=)
c.2596G= (p.Val866=)
3g.38585753C>GCA352141509SCN5Ac.2725G>C (p.Val909Leu)
c.2596G>C (p.Val866Leu)
3g.38585753C>TCA352141511SCN5Ac.2725G>A (p.Val909Met)
c.2596G>A (p.Val866Met)
dbSNP
3g.38585754C>ACA352141513SCN5Ac.2724G>T (p.Glu908Asp)
c.2595G>T (p.Glu865Asp)
3g.38585754C>GCA352141514SCN5Ac.2724G>C (p.Glu908Asp)
c.2595G>C (p.Glu865Asp)
3g.38585754C>TCA433332667SCN5Ac.2724G>A (p.Glu908=)
c.2595G>A (p.Glu865=)
ClinVar dbSNP
3g.38585755T>ACA352141516SCN5Ac.2723A>T (p.Glu908Val)
c.2594A>T (p.Glu865Val)
ClinVar
3g.38585755T>CCA352141520SCN5Ac.2723A>G (p.Glu908Gly)
c.2594A>G (p.Glu865Gly)
3g.38585755T>GCA352141518SCN5Ac.2723A>C (p.Glu908Ala)
c.2594A>C (p.Glu865Ala)
3g.38585756C>ACA352141521SCN5Ac.2722G>T (p.Glu908Ter)
c.2593G>T (p.Glu865Ter)
dbSNP
3g.38585756C=CA1358577409SCN5Ac.2722G= (p.Glu908=)
c.2593G= (p.Glu865=)
3g.38585756C>GCA352141523SCN5Ac.2722G>C (p.Glu908Gln)
c.2593G>C (p.Glu865Gln)
3g.38585756C>TCA352141525SCN5Ac.2722G>A (p.Glu908Lys)
c.2593G>A (p.Glu865Lys)
3g.38585757C>ACA352141527SCN5Ac.2721G>T (p.Met907Ile)
c.2592G>T (p.Met864Ile)
3g.38585757C=CA1358577410SCN5Ac.2721G= (p.Met907=)
c.2592G= (p.Met864=)
3g.38585757C>GCA352141528SCN5Ac.2721G>C (p.Met907Ile)
c.2592G>C (p.Met864Ile)
3g.38585757C>TCA352141529SCN5Ac.2721G>A (p.Met907Ile)
c.2592G>A (p.Met864Ile)
ClinVar dbSNP
3g.38585758A>CCA352141532SCN5Ac.2720T>G (p.Met907Arg)
c.2591T>G (p.Met864Arg)
3g.38585758A>GCA352141534SCN5Ac.2720T>C (p.Met907Thr)
c.2591T>C (p.Met864Thr)
3g.38585758A>TCA352141535SCN5Ac.2720T>A (p.Met907Lys)
c.2591T>A (p.Met864Lys)
3g.38585759T>ACA352141540SCN5Ac.2719A>T (p.Met907Leu)
c.2590A>T (p.Met864Leu)
3g.38585759T>CCA352141538SCN5Ac.2719A>G (p.Met907Val)
c.2590A>G (p.Met864Val)
ClinVar dbSNP
3g.38585759T>GCA352141536SCN5Ac.2719A>C (p.Met907Leu)
c.2590A>C (p.Met864Leu)
3g.38585760G>ACA060748SCN5Ac.2718C>T (p.Cys906=)
c.2589C>T (p.Cys863=)
dbSNP ExAC gnomAD v2 gnomAD v4

Number of alleles fetched