Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.38603921G>A | CA015163 | SCN5A | c.1681C>T (p.Leu561=) c.1552C>T (p.Leu518=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.38603921G>C | CA352146750 | SCN5A | c.1681C>G (p.Leu561Val) c.1552C>G (p.Leu518Val) | |
3 | g.38603921G= | CA1358584967 | SCN5A | c.1681C= (p.Leu561=) c.1552C= (p.Leu518=) | |
3 | g.38603921G>T | CA352146752 | SCN5A | c.1681C>A (p.Leu561Met) c.1552C>A (p.Leu518Met) | |
3 | g.38603922T>A | CA433333024 | SCN5A | c.1680A>T (p.Ser560=) c.1551A>T (p.Ser517=) | |
3 | g.38603922T>C | CA433333021 | SCN5A | c.1680A>G (p.Ser560=) c.1551A>G (p.Ser517=) | |
3 | g.38603922T>G | CA433333020 | SCN5A | c.1680A>C (p.Ser560=) c.1551A>C (p.Ser517=) | |
3 | g.38603923G>A | CA352146756 | SCN5A | c.1679C>T (p.Ser560Leu) c.1550C>T (p.Ser517Leu) | ClinVar |
3 | g.38603923G>C | CA352146759 | SCN5A | c.1679C>G (p.Ser560Ter) c.1550C>G (p.Ser517Ter) | ClinVar |
3 | g.38603923G>T | CA352146762 | SCN5A | c.1679C>A (p.Ser560Ter) c.1550C>A (p.Ser517Ter) | |
3 | g.38603924A>C | CA352146769 | SCN5A | c.1678T>G (p.Ser560Ala) c.1549T>G (p.Ser517Ala) | |
3 | g.38603924A>G | CA352146766 | SCN5A | c.1678T>C (p.Ser560Pro) c.1549T>C (p.Ser517Pro) | |
3 | g.38603924A>T | CA352146765 | SCN5A | c.1678T>A (p.Ser560Thr) c.1549T>A (p.Ser517Thr) | |
3 | g.38603925T>A | CA433333037 | SCN5A | c.1677A>T (p.Thr559=) c.1548A>T (p.Thr516=) | |
3 | g.38603925T>C | CA72939197 | SCN5A | c.1677A>G (p.Thr559=) c.1548A>G (p.Thr516=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
3 | g.38603925T>G | CA433333038 | SCN5A | c.1677A>C (p.Thr559=) c.1548A>C (p.Thr516=) | |
3 | g.38603925T= | CA1358584968 | SCN5A | c.1677A= (p.Thr559=) c.1548A= (p.Thr516=) | |
3 | g.38603926G>A | CA015154 | SCN5A | c.1676C>T (p.Thr559Ile) c.1547C>T (p.Thr516Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.38603926G>C | CA058488 | SCN5A | c.1676C>G (p.Thr559Arg) c.1547C>G (p.Thr516Arg) | dbSNP ExAC gnomAD v4 |
3 | g.38603926G= | CA1358584969 | SCN5A | c.1676C= (p.Thr559=) c.1547C= (p.Thr516=) | |
3 | g.38603926G>T | CA352146777 | SCN5A | c.1676C>A (p.Thr559Lys) c.1547C>A (p.Thr516Lys) | ClinVar dbSNP |
3 | g.38603927T>A | CA352146781 | SCN5A | c.1675A>T (p.Thr559Ser) c.1546A>T (p.Thr516Ser) | |
3 | g.38603927T>C | CA352146782 | SCN5A | c.1675A>G (p.Thr559Ala) c.1546A>G (p.Thr516Ala) | |
3 | g.38603927T>G | CA352146784 | SCN5A | c.1675A>C (p.Thr559Pro) c.1546A>C (p.Thr516Pro) | dbSNP |
3 | g.38603927T= | CA1358584970 | SCN5A | c.1675A= (p.Thr559=) c.1546A= (p.Thr516=) | |
3 | g.38603928G>A | CA433333049 | SCN5A | c.1674C>T (p.His558=) c.1545C>T (p.His515=) | |
3 | g.38603928G>C | CA352146786 | SCN5A | c.1674C>G (p.His558Gln) c.1545C>G (p.His515Gln) | ClinVar dbSNP |
3 | g.38603928G= | CA1358584971 | SCN5A | c.1674C= (p.His558=) c.1545C= (p.His515=) | |
3 | g.38603928G>T | CA352146788 | SCN5A | c.1674C>A (p.His558Gln) c.1545C>A (p.His515Gln) | |
3 | g.38603929T>A | CA352146790 | SCN5A | c.1673A>T (p.His558Leu) c.1544A>T (p.His515Leu) | |
3 | g.38603929T>C | CA015145 | SCN5A | c.1673A>G (p.His558Arg) c.1544A>G (p.His515Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.[38603929T>C;38604067G>A] | CA085349 | SCN5A | c.[1535C>T;1673A>G] (p.[Thr512Ile;His558Arg]) c.[1406C>T;1544A>G] (p.[Thr469Ile;His515Arg]) | |
3 | g.38603929T>G | CA352146796 | SCN5A | c.1673A>C (p.His558Pro) c.1544A>C (p.His515Pro) | |
3 | g.38603929T= | CA1358584972 | SCN5A | c.1673A= (p.His558=) c.1544A= (p.His515=) | |
3 | g.38603929_38603930delinsCA | CA1139655765 | SCN5A | c.1672_1673delinsTG (p.His558Cys) c.1543_1544delinsTG (p.His515Cys) | ClinVar |
3 | g.38603930G>A | CA72939207 | SCN5A | c.1672C>T (p.His558Tyr) c.1543C>T (p.His515Tyr) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
3 | g.38603930G>C | CA352146802 | SCN5A | c.1672C>G (p.His558Asp) c.1543C>G (p.His515Asp) | |
3 | g.38603930G= | CA1358584973 | SCN5A | c.1672C= (p.His558=) c.1543C= (p.His515=) | |
3 | g.38603930G>T | CA352146799 | SCN5A | c.1672C>A (p.His558Asn) c.1543C>A (p.His515Asn) | |
3 | g.38603931del | CA2586971911 | SCN5A | c.1672del (p.His558ThrfsTer?) c.1543del (p.His515ThrfsTer?) | gnomAD v4 |
3 | g.38603931G>A | CA433333057 | SCN5A | c.1671C>T (p.His557=) c.1542C>T (p.His514=) | gnomAD v4 |
3 | g.38603931G>C | CA058476 | SCN5A | c.1671C>G (p.His557Gln) c.1542C>G (p.His514Gln) | ClinVar dbSNP ExAC gnomAD v2 |
3 | g.38603931G= | CA1358584974 | SCN5A | c.1671C= (p.His557=) c.1542C= (p.His514=) | |
3 | g.38603931G>T | CA352146807 | SCN5A | c.1671C>A (p.His557Gln) c.1542C>A (p.His514Gln) | |
3 | g.38603932T>A | CA352146809 | SCN5A | c.1670A>T (p.His557Leu) c.1541A>T (p.His514Leu) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.38603932T>C | CA72939214 | SCN5A | c.1670A>G (p.His557Arg) c.1541A>G (p.His514Arg) | ClinVar dbSNP gnomAD v4 |
3 | g.38603932T>G | CA352146813 | SCN5A | c.1670A>C (p.His557Pro) c.1541A>C (p.His514Pro) | |
3 | g.38603932T= | CA1358584975 | SCN5A | c.1670A= (p.His557=) c.1541A= (p.His514=) | |
3 | g.38603933G>A | CA058468 | SCN5A | c.1669C>T (p.His557Tyr) c.1540C>T (p.His514Tyr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.38603933G>C | CA352146817 | SCN5A | c.1669C>G (p.His557Asp) c.1540C>G (p.His514Asp) |