Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.73329619G>A | CA393093521 | HCN4 | c.1544C>T (p.Ala515Val) c.326C>T (p.Ala109Val) | |
15 | g.73329619G>C | CA393093524 | HCN4 | c.1544C>G (p.Ala515Gly) c.326C>G (p.Ala109Gly) | |
15 | g.73329619G>T | CA393093522 | HCN4 | c.1544C>A (p.Ala515Asp) c.326C>A (p.Ala109Asp) | |
15 | g.73329620C>A | CA393093527 | HCN4 | c.1543G>T (p.Ala515Ser) c.325G>T (p.Ala109Ser) | |
15 | g.73329620C>G | CA393093529 | HCN4 | c.1543G>C (p.Ala515Pro) c.325G>C (p.Ala109Pro) | |
15 | g.73329620C>T | CA393093531 | HCN4 | c.1543G>A (p.Ala515Thr) c.325G>A (p.Ala109Thr) | |
15 | g.73329621A>C | CA491151476 | HCN4 | c.1542T>G (p.Thr514=) c.324T>G (p.Thr108=) | |
15 | g.73329621A>G | CA491151478 | HCN4 | c.1542T>C (p.Thr514=) c.324T>C (p.Thr108=) | |
15 | g.73329621A>T | CA491151477 | HCN4 | c.1542T>A (p.Thr514=) c.324T>A (p.Thr108=) | |
15 | g.73329622G>A | CA393093533 | HCN4 | c.1541C>T (p.Thr514Ile) c.323C>T (p.Thr108Ile) | |
15 | g.73329622G>C | CA393093534 | HCN4 | c.1541C>G (p.Thr514Ser) c.323C>G (p.Thr108Ser) | |
15 | g.73329622G>T | CA393093536 | HCN4 | c.1541C>A (p.Thr514Asn) c.323C>A (p.Thr108Asn) | |
15 | g.73329623T>A | CA393093538 | HCN4 | c.1540A>T (p.Thr514Ser) c.322A>T (p.Thr108Ser) | |
15 | g.73329623T>C | CA393093541 | HCN4 | c.1540A>G (p.Thr514Ala) c.322A>G (p.Thr108Ala) | COSMIC |
15 | g.73329623T>G | CA393093543 | HCN4 | c.1540A>C (p.Thr514Pro) c.322A>C (p.Thr108Pro) | |
15 | g.73329624G>A | CA491151479 | HCN4 | c.1539C>T (p.Ala513=) c.321C>T (p.Ala107=) | |
15 | g.73329624G>C | CA491151480 | HCN4 | c.1539C>G (p.Ala513=) c.321C>G (p.Ala107=) | |
15 | g.73329624G>T | CA491151481 | HCN4 | c.1539C>A (p.Ala513=) c.321C>A (p.Ala107=) | |
15 | g.73329625G>A | CA393093549 | HCN4 | c.1538C>T (p.Ala513Val) c.320C>T (p.Ala107Val) | |
15 | g.73329625G>C | CA393093547 | HCN4 | c.1538C>G (p.Ala513Gly) c.320C>G (p.Ala107Gly) | |
15 | g.73329625G>T | CA393093545 | HCN4 | c.1538C>A (p.Ala513Asp) c.320C>A (p.Ala107Asp) | |
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) |