Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.73329626C>A | CA393093552 | HCN4 | c.1537G>T (p.Ala513Ser) c.319G>T (p.Ala107Ser) | |
15 | g.73329626C= | CA2187167446 | HCN4 | c.1537G= (p.Ala513=) c.319G= (p.Ala107=) | |
15 | g.73329626C>G | CA393093553 | HCN4 | c.1537G>C (p.Ala513Pro) c.319G>C (p.Ala107Pro) | |
15 | g.73329626C>T | CA393093555 | HCN4 | c.1537G>A (p.Ala513Thr) c.319G>A (p.Ala107Thr) | dbSNP gnomAD v3 gnomAD v4 |
15 | g.73329627G>A | CA7649283 | HCN4 | c.1536C>T (p.His512=) c.318C>T (p.His106=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
15 | g.73329627G>C | CA393093558 | HCN4 | c.1536C>G (p.His512Gln) c.318C>G (p.His106Gln) | |
15 | g.73329627G= | CA2187167452 | HCN4 | c.1536C= (p.His512=) c.318C= (p.His106=) | |
15 | g.73329627G>T | CA393093560 | HCN4 | c.1536C>A (p.His512Gln) c.318C>A (p.His106Gln) | |
15 | g.73329628T>A | CA393093562 | HCN4 | c.1535A>T (p.His512Leu) c.317A>T (p.His106Leu) | |
15 | g.73329628T>C | CA393093564 | HCN4 | c.1535A>G (p.His512Arg) c.317A>G (p.His106Arg) | |
15 | g.73329628T>G | CA393093566 | HCN4 | c.1535A>C (p.His512Pro) c.317A>C (p.His106Pro) | |
15 | g.73329629G>A | CA393093568 | HCN4 | c.1534C>T (p.His512Tyr) c.316C>T (p.His106Tyr) | |
15 | g.73329629G>C | CA393093570 | HCN4 | c.1534C>G (p.His512Asp) c.316C>G (p.His106Asp) | |
15 | g.73329629G>T | CA393093572 | HCN4 | c.1534C>A (p.His512Asn) c.316C>A (p.His106Asn) | |
15 | g.73329630G>A | CA491151484 | HCN4 | c.1533C>T (p.Gly511=) c.315C>T (p.Gly105=) | gnomAD v4 |
15 | g.73329630G>C | CA491151482 | HCN4 | c.1533C>G (p.Gly511=) c.315C>G (p.Gly105=) | |
15 | g.73329630G>T | CA491151483 | HCN4 | c.1533C>A (p.Gly511=) c.315C>A (p.Gly105=) | ClinVar dbSNP gnomAD v4 |
15 | g.73329631C>A | CA393093579 | HCN4 | c.1532G>T (p.Gly511Val) c.314G>T (p.Gly105Val) | |
15 | g.73329631C>G | CA393093576 | HCN4 | c.1532G>C (p.Gly511Ala) c.314G>C (p.Gly105Ala) | gnomAD v4 |
15 | g.73329631C>T | CA393093574 | HCN4 | c.1532G>A (p.Gly511Asp) c.314G>A (p.Gly105Asp) | |
15 | g.73329632C>A | CA393093581 | HCN4 | c.1531G>T (p.Gly511Cys) c.313G>T (p.Gly105Cys) | |
15 | g.73329632C>G | CA393093582 | HCN4 | c.1531G>C (p.Gly511Arg) c.313G>C (p.Gly105Arg) | |
15 | g.73329632C>T | CA393093584 | HCN4 | c.1531G>A (p.Gly511Ser) c.313G>A (p.Gly105Ser) | |
15 | g.73329633A>C | CA393093586 | HCN4 | c.1530T>G (p.Ile510Met) c.312T>G (p.Ile104Met) | |
15 | g.73329633A>G | CA491151485 | HCN4 | c.1530T>C (p.Ile510=) c.312T>C (p.Ile104=) | |
15 | g.73329633A>T | CA491151486 | HCN4 | c.1530T>A (p.Ile510=) c.312T>A (p.Ile104=) | |
15 | g.73329634A>C | CA393093589 | HCN4 | c.1529T>G (p.Ile510Ser) c.311T>G (p.Ile104Ser) | |
15 | g.73329634A>G | CA393093591 | HCN4 | c.1529T>C (p.Ile510Thr) c.311T>C (p.Ile104Thr) | |
15 | g.73329634A>T | CA393093593 | HCN4 | c.1529T>A (p.Ile510Asn) c.311T>A (p.Ile104Asn) | |
15 | g.73329635T>A | CA393093596 | HCN4 | c.1528A>T (p.Ile510Phe) c.310A>T (p.Ile104Phe) | |
15 | g.73329635T>C | CA393093598 | HCN4 | c.1528A>G (p.Ile510Val) c.310A>G (p.Ile104Val) | |
15 | g.73329635T>G | CA393093600 | HCN4 | c.1528A>C (p.Ile510Leu) c.310A>C (p.Ile104Leu) | |
15 | g.73329636G>A | CA491151487 | HCN4 | c.1527C>T (p.Phe509=) c.309C>T (p.Phe103=) | |
15 | g.73329636G>C | CA393093602 | HCN4 | c.1527C>G (p.Phe509Leu) c.309C>G (p.Phe103Leu) | |
15 | g.73329636G>T | CA393093604 | HCN4 | c.1527C>A (p.Phe509Leu) c.309C>A (p.Phe103Leu) | |
15 | g.73329637A>C | CA393093606 | HCN4 | c.1526T>G (p.Phe509Cys) c.308T>G (p.Phe103Cys) | |
15 | g.73329637A>G | CA393093610 | HCN4 | c.1526T>C (p.Phe509Ser) c.308T>C (p.Phe103Ser) | |
15 | g.73329637A>T | CA393093608 | HCN4 | c.1526T>A (p.Phe509Tyr) c.308T>A (p.Phe103Tyr) | |
15 | g.73329638A>C | CA393093612 | HCN4 | c.1525T>G (p.Phe509Val) c.307T>G (p.Phe103Val) | |
15 | g.73329638A>G | CA393093615 | HCN4 | c.1525T>C (p.Phe509Leu) c.307T>C (p.Phe103Leu) | gnomAD v4 |
15 | g.73329638A>T | CA393093613 | HCN4 | c.1525T>A (p.Phe509Ile) c.307T>A (p.Phe103Ile) | |
15 | g.73329639C>A | CA393093618 | HCN4 | c.1524G>T (p.Met508Ile) c.306G>T (p.Met102Ile) | |
15 | g.73329639C>G | CA393093622 | HCN4 | c.1524G>C (p.Met508Ile) c.306G>C (p.Met102Ile) | |
15 | g.73329639C>T | CA393093619 | HCN4 | c.1524G>A (p.Met508Ile) c.306G>A (p.Met102Ile) | |
15 | g.73329640A>C | CA393093623 | HCN4 | c.1523T>G (p.Met508Arg) c.305T>G (p.Met102Arg) | |
15 | g.73329640A>G | CA393093625 | HCN4 | c.1523T>C (p.Met508Thr) c.305T>C (p.Met102Thr) | gnomAD v4 |
15 | g.73329640A>T | CA393093627 | HCN4 | c.1523T>A (p.Met508Lys) c.305T>A (p.Met102Lys) | |
15 | g.73329641T>A | CA393093630 | HCN4 | c.1522A>T (p.Met508Leu) c.304A>T (p.Met102Leu) | |
15 | g.73329641T>C | CA272672022 | HCN4 | c.1522A>G (p.Met508Val) c.304A>G (p.Met102Val) | ClinVar dbSNP |
15 | g.73329641T>G | CA393093633 | HCN4 | c.1522A>C (p.Met508Leu) c.304A>C (p.Met102Leu) |