Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.38603913C>A | CA433332971 | SCN5A | c.1689G>T (p.Val563=) c.1560G>T (p.Val520=) | |
3 | g.38603913C>G | CA433332972 | SCN5A | c.1689G>C (p.Val563=) c.1560G>C (p.Val520=) | |
3 | g.38603913C>T | CA433332973 | SCN5A | c.1689G>A (p.Val563=) c.1560G>A (p.Val520=) | gnomAD v4 |
3 | g.38603914A= | CA1358584964 | SCN5A | c.1688T= (p.Val563=) c.1559T= (p.Val520=) | |
3 | g.38603914A>C | CA352146709 | SCN5A | c.1688T>G (p.Val563Gly) c.1559T>G (p.Val520Gly) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.38603914A>G | CA352146712 | SCN5A | c.1688T>C (p.Val563Ala) c.1559T>C (p.Val520Ala) | |
3 | g.38603914A>T | CA352146714 | SCN5A | c.1688T>A (p.Val563Glu) c.1559T>A (p.Val520Glu) | |
3 | g.38603915C>A | CA352146717 | SCN5A | c.1687G>T (p.Val563Leu) c.1558G>T (p.Val520Leu) | ClinVar dbSNP gnomAD v4 |
3 | g.38603915C>G | CA352146720 | SCN5A | c.1687G>C (p.Val563Leu) c.1558G>C (p.Val520Leu) | gnomAD v4 |
3 | g.38603915C>T | CA352146722 | SCN5A | c.1687G>A (p.Val563Met) c.1558G>A (p.Val520Met) | |
3 | g.38603916dup | CA2990484004 | SCN5A | c.1687dup (p.Val563GlyfsTer?) c.1558dup (p.Val520GlyfsTer?) | |
3 | g.38603916C>A | CA433332986 | SCN5A | c.1686G>T (p.Leu562=) c.1557G>T (p.Leu519=) | |
3 | g.38603916C>G | CA433332988 | SCN5A | c.1686G>C (p.Leu562=) c.1557G>C (p.Leu519=) | |
3 | g.38603916C>T | CA433332992 | SCN5A | c.1686G>A (p.Leu562=) c.1557G>A (p.Leu519=) | |
3 | g.38603917A>C | CA352146727 | SCN5A | c.1685T>G (p.Leu562Arg) c.1556T>G (p.Leu519Arg) | |
3 | g.38603917A>G | CA352146731 | SCN5A | c.1685T>C (p.Leu562Pro) c.1556T>C (p.Leu519Pro) | gnomAD v4 |
3 | g.38603917A>T | CA352146729 | SCN5A | c.1685T>A (p.Leu562Gln) c.1556T>A (p.Leu519Gln) | |
3 | g.38603918G>A | CA433333007 | SCN5A | c.1684C>T (p.Leu562=) c.1555C>T (p.Leu519=) | dbSNP gnomAD v2 |
3 | g.38603918G>C | CA352146734 | SCN5A | c.1684C>G (p.Leu562Val) c.1555C>G (p.Leu519Val) | |
3 | g.38603918G= | CA1358584965 | SCN5A | c.1684C= (p.Leu562=) c.1555C= (p.Leu519=) | |
3 | g.38603918G>T | CA352146737 | SCN5A | c.1684C>A (p.Leu562Met) c.1555C>A (p.Leu519Met) | |
3 | g.38603919C>A | CA433333010 | SCN5A | c.1683G>T (p.Leu561=) c.1554G>T (p.Leu518=) | |
3 | g.38603919C= | CA1358584966 | SCN5A | c.1683G= (p.Leu561=) c.1554G= (p.Leu518=) | |
3 | g.38603919C>G | CA433333013 | SCN5A | c.1683G>C (p.Leu561=) c.1554G>C (p.Leu518=) | |
3 | g.38603919C>T | CA433333012 | SCN5A | c.1683G>A (p.Leu561=) c.1554G>A (p.Leu518=) | dbSNP gnomAD v2 gnomAD v4 |
3 | g.38603920A>C | CA352146740 | SCN5A | c.1682T>G (p.Leu561Arg) c.1553T>G (p.Leu518Arg) | |
3 | g.38603920A>G | CA352146742 | SCN5A | c.1682T>C (p.Leu561Pro) c.1553T>C (p.Leu518Pro) | |
3 | g.38603920A>T | CA352146745 | SCN5A | c.1682T>A (p.Leu561Gln) c.1553T>A (p.Leu518Gln) | |
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) |