UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 15 | g.73329604A>C | CA393093456 | HCN4 | c.1559T>G (p.Leu520Arg) c.341T>G (p.Leu114Arg) | |
| 15 | g.73329604A>G | CA393093458 | HCN4 | c.1559T>C (p.Leu520Pro) c.341T>C (p.Leu114Pro) | |
| 15 | g.73329604A>T | CA393093460 | HCN4 | c.1559T>A (p.Leu520Gln) c.341T>A (p.Leu114Gln) | |
| 15 | g.73329605G>A | CA291166 | HCN4 | c.1558C>T (p.Leu520=) c.340C>T (p.Leu114=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73329605G>C | CA393093464 | HCN4 | c.1558C>G (p.Leu520Val) c.340C>G (p.Leu114Val) | |
| 15 | g.73329605G= | CA2187167423 | HCN4 | c.1558C= (p.Leu520=) c.340C= (p.Leu114=) | |
| 15 | g.73329605G>T | CA393093465 | HCN4 | c.1558C>A (p.Leu520Met) c.340C>A (p.Leu114Met) | |
| 15 | g.73329606G>A | CA491151465 | HCN4 | c.1557C>T (p.Ser519=) c.339C>T (p.Ser113=) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73329606G>C | CA491151466 | HCN4 | c.1557C>G (p.Ser519=) c.339C>G (p.Ser113=) | |
| 15 | g.73329606G= | CA2187167428 | HCN4 | c.1557C= (p.Ser519=) c.339C= (p.Ser113=) | |
| 15 | g.73329606G>T | CA491151467 | HCN4 | c.1557C>A (p.Ser519=) c.339C>A (p.Ser113=) | |
| 15 | g.73329607G>A | CA393093466 | HCN4 | c.1556C>T (p.Ser519Phe) c.338C>T (p.Ser113Phe) | |
| 15 | g.73329607G>C | CA393093467 | HCN4 | c.1556C>G (p.Ser519Cys) c.338C>G (p.Ser113Cys) | COSMIC |
| 15 | g.73329607G>T | CA393093469 | HCN4 | c.1556C>A (p.Ser519Tyr) c.338C>A (p.Ser113Tyr) | |
| 15 | g.73329608A>C | CA393093472 | HCN4 | c.1555T>G (p.Ser519Ala) c.337T>G (p.Ser113Ala) | |
| 15 | g.73329608A>G | CA393093473 | HCN4 | c.1555T>C (p.Ser519Pro) c.337T>C (p.Ser113Pro) | |
| 15 | g.73329608A>T | CA393093475 | HCN4 | c.1555T>A (p.Ser519Thr) c.337T>A (p.Ser113Thr) | |
| 15 | g.73329609C>A | CA393093477 | HCN4 | c.1554G>T (p.Gln518His) c.336G>T (p.Gln112His) | |
| 15 | g.73329609C>G | CA393093479 | HCN4 | c.1554G>C (p.Gln518His) c.336G>C (p.Gln112His) | |
| 15 | g.73329609C>T | CA491151468 | HCN4 | c.1554G>A (p.Gln518=) c.336G>A (p.Gln112=) | |
| 15 | g.73329610T>A | CA393093484 | HCN4 | c.1553A>T (p.Gln518Leu) c.335A>T (p.Gln112Leu) | |
| 15 | g.73329610T>C | CA393093486 | HCN4 | c.1553A>G (p.Gln518Arg) c.335A>G (p.Gln112Arg) | gnomAD v4 |
| 15 | g.73329610T>G | CA393093482 | HCN4 | c.1553A>C (p.Gln518Pro) c.335A>C (p.Gln112Pro) | |
| 15 | g.73329611G>A | CA393093489 | HCN4 | c.1552C>T (p.Gln518Ter) c.334C>T (p.Gln112Ter) | |
| 15 | g.73329611G>C | CA393093492 | HCN4 | c.1552C>G (p.Gln518Glu) c.334C>G (p.Gln112Glu) | |
| 15 | g.73329611G>T | CA393093491 | HCN4 | c.1552C>A (p.Gln518Lys) c.334C>A (p.Gln112Lys) | |
| 15 | g.73329612G>A | CA491151469 | HCN4 | c.1551C>T (p.Ile517=) c.333C>T (p.Ile111=) | ClinVar |
| 15 | g.73329612G>C | CA393093495 | HCN4 | c.1551C>G (p.Ile517Met) c.333C>G (p.Ile111Met) | |
| 15 | g.73329612G>T | CA491151470 | HCN4 | c.1551C>A (p.Ile517=) c.333C>A (p.Ile111=) | |
| 15 | g.73329613A>C | CA393093498 | HCN4 | c.1550T>G (p.Ile517Ser) c.332T>G (p.Ile111Ser) | |
| 15 | g.73329613A>G | CA393093500 | HCN4 | c.1550T>C (p.Ile517Thr) c.332T>C (p.Ile111Thr) | |
| 15 | g.73329613A>T | CA393093501 | HCN4 | c.1550T>A (p.Ile517Asn) c.332T>A (p.Ile111Asn) | |
| 15 | g.73329614T>A | CA393093503 | HCN4 | c.1549A>T (p.Ile517Phe) c.331A>T (p.Ile111Phe) | |
| 15 | g.73329614T>C | CA393093505 | HCN4 | c.1549A>G (p.Ile517Val) c.331A>G (p.Ile111Val) | dbSNP gnomAD v4 |
| 15 | g.73329614T>G | CA393093506 | HCN4 | c.1549A>C (p.Ile517Leu) c.331A>C (p.Ile111Leu) | |
| 15 | g.73329614T= | CA2187167432 | HCN4 | c.1549A= (p.Ile517=) c.331A= (p.Ile111=) | |
| 15 | g.73329615G>A | CA16614561 | HCN4 | c.1548C>T (p.Leu516=) c.330C>T (p.Leu110=) | ClinVar dbSNP |
| 15 | g.73329615G>C | CA491151472 | HCN4 | c.1548C>G (p.Leu516=) c.330C>G (p.Leu110=) | |
| 15 | g.73329615G= | CA2187167435 | HCN4 | c.1548C= (p.Leu516=) c.330C= (p.Leu110=) | |
| 15 | g.73329615G>T | CA491151471 | HCN4 | c.1548C>A (p.Leu516=) c.330C>A (p.Leu110=) | |
| 15 | g.73329616A>C | CA393093509 | HCN4 | c.1547T>G (p.Leu516Arg) c.329T>G (p.Leu110Arg) | |
| 15 | g.73329616A>G | CA393093510 | HCN4 | c.1547T>C (p.Leu516Pro) c.329T>C (p.Leu110Pro) | |
| 15 | g.73329616A>T | CA393093512 | HCN4 | c.1547T>A (p.Leu516His) c.329T>A (p.Leu110His) | |
| 15 | g.73329617G>A | CA393093514 | HCN4 | c.1546C>T (p.Leu516Phe) c.328C>T (p.Leu110Phe) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73329617G>C | CA393093516 | HCN4 | c.1546C>G (p.Leu516Val) c.328C>G (p.Leu110Val) | |
| 15 | g.73329617G= | CA2187167439 | HCN4 | c.1546C= (p.Leu516=) c.328C= (p.Leu110=) | |
| 15 | g.73329617G>T | CA393093518 | HCN4 | c.1546C>A (p.Leu516Ile) c.328C>A (p.Leu110Ile) | |
| 15 | g.73329618G>A | CA491151473 | HCN4 | c.1545C>T (p.Ala515=) c.327C>T (p.Ala109=) | |
| 15 | g.73329618G>C | CA491151474 | HCN4 | c.1545C>G (p.Ala515=) c.327C>G (p.Ala109=) | dbSNP |
| 15 | g.73329618G= | CA2187167443 | HCN4 | c.1545C= (p.Ala515=) c.327C= (p.Ala109=) | |
| 15 | g.73329618G>T | CA491151475 | HCN4 | c.1545C>A (p.Ala515=) c.327C>A (p.Ala109=) | |
| 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) | |
| 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) | |
| 15 | g.73329641T= | CA2187167457 | HCN4 | c.1522A= (p.Met508=) c.304A= (p.Met102=) | |
| 15 | g.73329641dup | CA2695220988 | HCN4 | c.1522dup (p.Met508AsnfsTer?) c.304dup (p.Met102AsnfsTer?) | |
| 15 | g.73329642G>A | CA272672032 | HCN4 | c.1521C>T (p.Ala507=) c.303C>T (p.Ala101=) | ClinVar dbSNP |
| 15 | g.73329642G>C | CA491151488 | HCN4 | c.1521C>G (p.Ala507=) c.303C>G (p.Ala101=) | |
| 15 | g.73329642G= | CA2187167461 | HCN4 | c.1521C= (p.Ala507=) c.303C= (p.Ala101=) | |
| 15 | g.73329642G>T | CA491151489 | HCN4 | c.1521C>A (p.Ala507=) c.303C>A (p.Ala101=) | |
| 15 | g.73329643G>A | CA393093636 | HCN4 | c.1520C>T (p.Ala507Val) c.302C>T (p.Ala101Val) | |
| 15 | g.73329643G>C | CA393093638 | HCN4 | c.1520C>G (p.Ala507Gly) c.302C>G (p.Ala101Gly) | |
| 15 | g.73329643G>T | CA393093639 | HCN4 | c.1520C>A (p.Ala507Asp) c.302C>A (p.Ala101Asp) | |
| 15 | g.73329644C>A | CA393093642 | HCN4 | c.1519G>T (p.Ala507Ser) c.301G>T (p.Ala101Ser) | COSMIC |
| 15 | g.73329644C= | CA2187167464 | HCN4 | c.1519G= (p.Ala507=) c.301G= (p.Ala101=) | |
| 15 | g.73329644C>G | CA393093644 | HCN4 | c.1519G>C (p.Ala507Pro) c.301G>C (p.Ala101Pro) | |
| 15 | g.73329644C>T | CA393093645 | HCN4 | c.1519G>A (p.Ala507Thr) c.301G>A (p.Ala101Thr) | dbSNP gnomAD v4 |
| 15 | g.73329645G>A | CA202780 | HCN4 | c.1518C>T (p.Tyr506=) c.300C>T (p.Tyr100=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73329645G>C | CA393093651 | HCN4 | c.1518C>G (p.Tyr506Ter) c.300C>G (p.Tyr100Ter) | |
| 15 | g.73329645G= | CA2187167471 | HCN4 | c.1518C= (p.Tyr506=) c.300C= (p.Tyr100=) | |
| 15 | g.73329645G>T | CA393093650 | HCN4 | c.1518C>A (p.Tyr506Ter) c.300C>A (p.Tyr100Ter) | |
| 15 | g.73329646T>A | CA393093653 | HCN4 | c.1517A>T (p.Tyr506Phe) c.299A>T (p.Tyr100Phe) | |
| 15 | g.73329646T>C | CA393093655 | HCN4 | c.1517A>G (p.Tyr506Cys) c.299A>G (p.Tyr100Cys) | |
| 15 | g.73329646T>G | CA393093657 | HCN4 | c.1517A>C (p.Tyr506Ser) c.299A>C (p.Tyr100Ser) | |
| 15 | g.73329647A>C | CA393093659 | HCN4 | c.1516T>G (p.Tyr506Asp) c.298T>G (p.Tyr100Asp) | |
| 15 | g.73329647A>G | CA393093661 | HCN4 | c.1516T>C (p.Tyr506His) c.298T>C (p.Tyr100His) | |
| 15 | g.73329647A>T | CA393093663 | HCN4 | c.1516T>A (p.Tyr506Asn) c.298T>A (p.Tyr100Asn) | |
| 15 | g.73329648G>A | CA491151490 | HCN4 | c.1515C>T (p.Cys505=) c.297C>T (p.Cys99=) | |
| 15 | g.73329648G>C | CA393093665 | HCN4 | c.1515C>G (p.Cys505Trp) c.297C>G (p.Cys99Trp) | |
| 15 | g.73329648G>T | CA393093667 | HCN4 | c.1515C>A (p.Cys505Ter) c.297C>A (p.Cys99Ter) | |
| 15 | g.73329649C>A | CA393093670 | HCN4 | c.1514G>T (p.Cys505Phe) c.296G>T (p.Cys99Phe) | gnomAD v4 |
| 15 | g.73329649C>G | CA393093672 | HCN4 | c.1514G>C (p.Cys505Ser) c.296G>C (p.Cys99Ser) | |
| 15 | g.73329649C>T | CA393093674 | HCN4 | c.1514G>A (p.Cys505Tyr) c.296G>A (p.Cys99Tyr) | ClinVar |
| 15 | g.73329650A>C | CA393093680 | HCN4 | c.1513T>G (p.Cys505Gly) c.295T>G (p.Cys99Gly) | |
| 15 | g.73329650A>G | CA393093678 | HCN4 | c.1513T>C (p.Cys505Arg) c.295T>C (p.Cys99Arg) | |
| 15 | g.73329650A>T | CA393093675 | HCN4 | c.1513T>A (p.Cys505Ser) c.295T>A (p.Cys99Ser) | |
| 15 | g.73329651G>A | CA7649284 | HCN4 | c.1512C>T (p.Thr504=) c.294C>T (p.Thr98=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73329651G>C | CA491151494 | HCN4 | c.1512C>G (p.Thr504=) c.294C>G (p.Thr98=) | |
| 15 | g.73329651G= | CA2187167473 | HCN4 | c.1512C= (p.Thr504=) c.294C= (p.Thr98=) | |
| 15 | g.73329651G>T | CA491151496 | HCN4 | c.1512C>A (p.Thr504=) c.294C>A (p.Thr98=) | |
| 15 | g.73329652G>A | CA393093682 | HCN4 | c.1511C>T (p.Thr504Ile) c.293C>T (p.Thr98Ile) | |
| 15 | g.73329652G>C | CA393093684 | HCN4 | c.1511C>G (p.Thr504Ser) c.293C>G (p.Thr98Ser) | |
| 15 | g.73329652G= | CA2187167477 | HCN4 | c.1511C= (p.Thr504=) c.293C= (p.Thr98=) | |
| 15 | g.73329652G>T | CA393093686 | HCN4 | c.1511C>A (p.Thr504Asn) c.293C>A (p.Thr98Asn) | ClinVar dbSNP |
| 15 | g.73329653T>A | CA393093689 | HCN4 | c.1510A>T (p.Thr504Ser) c.292A>T (p.Thr98Ser) | |
| 15 | g.73329653T>C | CA393093690 | HCN4 | c.1510A>G (p.Thr504Ala) c.292A>G (p.Thr98Ala) | |
| 15 | g.73329653T>G | CA393093692 | HCN4 | c.1510A>C (p.Thr504Pro) c.292A>C (p.Thr98Pro) | dbSNP |
| 15 | g.73329653T= | CA2187167481 | HCN4 | c.1510A= (p.Thr504=) c.292A= (p.Thr98=) | |
| 15 | g.73329654G>A | CA16614505 | HCN4 | c.1509C>T (p.Ala503=) c.291C>T (p.Ala97=) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73329654G>C | CA491151506 | HCN4 | c.1509C>G (p.Ala503=) c.291C>G (p.Ala97=) | |
| 15 | g.73329654G= | CA2187167486 | HCN4 | c.1509C= (p.Ala503=) c.291C= (p.Ala97=) | |
| 15 | g.73329654G>T | CA491151508 | HCN4 | c.1509C>A (p.Ala503=) c.291C>A (p.Ala97=) | |
| 15 | g.73329655G>A | CA393093695 | HCN4 | c.1508C>T (p.Ala503Val) c.290C>T (p.Ala97Val) | gnomAD v4 |
| 15 | g.73329655G>C | CA393093698 | HCN4 | c.1508C>G (p.Ala503Gly) c.290C>G (p.Ala97Gly) | |
| 15 | g.73329655G>T | CA393093699 | HCN4 | c.1508C>A (p.Ala503Asp) c.290C>A (p.Ala97Asp) | |
| 15 | g.73329656C>A | CA393093700 | HCN4 | c.1507G>T (p.Ala503Ser) c.289G>T (p.Ala97Ser) | |
| 15 | g.73329656C>G | CA393093702 | HCN4 | c.1507G>C (p.Ala503Pro) c.289G>C (p.Ala97Pro) | |
| 15 | g.73329656C>T | CA393093704 | HCN4 | c.1507G>A (p.Ala503Thr) c.289G>A (p.Ala97Thr) | |
| 15 | g.73329657A>C | CA491151517 | HCN4 | c.1506T>G (p.Gly502=) c.288T>G (p.Gly96=) | |
| 15 | g.73329657A>G | CA491151516 | HCN4 | c.1506T>C (p.Gly502=) c.288T>C (p.Gly96=) | |
| 15 | g.73329657A>T | CA491151519 | HCN4 | c.1506T>A (p.Gly502=) c.288T>A (p.Gly96=) | |
| 15 | g.73329658C>A | CA393093709 | HCN4 | c.1505G>T (p.Gly502Val) c.287G>T (p.Gly96Val) | |
| 15 | g.73329658C>G | CA393093710 | HCN4 | c.1505G>C (p.Gly502Ala) c.287G>C (p.Gly96Ala) | |
| 15 | g.73329658C>T | CA393093707 | HCN4 | c.1505G>A (p.Gly502Asp) c.287G>A (p.Gly96Asp) | |
| 15 | g.73329659C>A | CA393093713 | HCN4 | c.1504G>T (p.Gly502Cys) c.286G>T (p.Gly96Cys) | |
| 15 | g.73329659C>G | CA393093714 | HCN4 | c.1504G>C (p.Gly502Arg) c.286G>C (p.Gly96Arg) | |
| 15 | g.73329659C>T | CA393093716 | HCN4 | c.1504G>A (p.Gly502Ser) c.286G>A (p.Gly96Ser) | |
| 15 | g.73329660C>A | CA491151527 | HCN4 | c.1503G>T (p.Val501=) c.285G>T (p.Val95=) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73329660C= | CA2187167492 | HCN4 | c.1503G= (p.Val501=) c.285G= (p.Val95=) | |
| 15 | g.73329660C>G | CA491151529 | HCN4 | c.1503G>C (p.Val501=) c.285G>C (p.Val95=) | |
| 15 | g.73329660C>T | CA491151531 | HCN4 | c.1503G>A (p.Val501=) c.285G>A (p.Val95=) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73329661A>C | CA393093718 | HCN4 | c.1502T>G (p.Val501Gly) c.284T>G (p.Val95Gly) | |
| 15 | g.73329661A>G | CA393093719 | HCN4 | c.1502T>C (p.Val501Ala) c.284T>C (p.Val95Ala) | |
| 15 | g.73329661A>T | CA393093721 | HCN4 | c.1502T>A (p.Val501Glu) c.284T>A (p.Val95Glu) | |
| 15 | g.73329662C>A | CA393093723 | HCN4 | c.1501G>T (p.Val501Leu) c.283G>T (p.Val95Leu) | |
| 15 | g.73329662C>G | CA393093726 | HCN4 | c.1501G>C (p.Val501Leu) c.283G>C (p.Val95Leu) | |
| 15 | g.73329662C>T | CA393093725 | HCN4 | c.1501G>A (p.Val501Met) c.283G>A (p.Val95Met) | COSMIC |
| 15 | g.73329663G>A | CA7649285 | HCN4 | c.1500C>T (p.Ile500=) c.282C>T (p.Ile94=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73329663G>C | CA393093729 | HCN4 | c.1500C>G (p.Ile500Met) c.282C>G (p.Ile94Met) | |
| 15 | g.73329663G= | CA2187167495 | HCN4 | c.1500C= (p.Ile500=) c.282C= (p.Ile94=) | |
| 15 | g.73329663G>T | CA491151543 | HCN4 | c.1500C>A (p.Ile500=) c.282C>A (p.Ile94=) | |
| 15 | g.73329664A>C | CA393093731 | HCN4 | c.1499T>G (p.Ile500Ser) c.281T>G (p.Ile94Ser) | |
| 15 | g.73329664A>G | CA393093732 | HCN4 | c.1499T>C (p.Ile500Thr) c.281T>C (p.Ile94Thr) | |
| 15 | g.73329664A>T | CA393093735 | HCN4 | c.1499T>A (p.Ile500Asn) c.281T>A (p.Ile94Asn) | |
| 15 | g.73329665T>A | CA393093738 | HCN4 | c.1498A>T (p.Ile500Phe) c.280A>T (p.Ile94Phe) | |
| 15 | g.73329665T>C | CA393093739 | HCN4 | c.1498A>G (p.Ile500Val) c.280A>G (p.Ile94Val) | |
| 15 | g.73329665T>G | CA393093737 | HCN4 | c.1498A>C (p.Ile500Leu) c.280A>C (p.Ile94Leu) | |
| 15 | g.73329666C>A | CA393093740 | HCN4 | c.1497G>T (p.Met499Ile) c.279G>T (p.Met93Ile) | |
| 15 | g.73329666C>G | CA393093742 | HCN4 | c.1497G>C (p.Met499Ile) c.279G>C (p.Met93Ile) | |
| 15 | g.73329666C>T | CA393093741 | HCN4 | c.1497G>A (p.Met499Ile) c.279G>A (p.Met93Ile) | |
| 15 | g.73329667A>C | CA393093743 | HCN4 | c.1496T>G (p.Met499Arg) c.278T>G (p.Met93Arg) | |
| 15 | g.73329667A>G | CA393093744 | HCN4 | c.1496T>C (p.Met499Thr) c.278T>C (p.Met93Thr) | |
| 15 | g.73329667A>T | CA393093745 | HCN4 | c.1496T>A (p.Met499Lys) c.278T>A (p.Met93Lys) | |
| 15 | g.73329668T>A | CA393093746 | HCN4 | c.1495A>T (p.Met499Leu) c.277A>T (p.Met93Leu) | |
| 15 | g.73329668T>C | CA393093747 | HCN4 | c.1495A>G (p.Met499Val) c.277A>G (p.Met93Val) | |
| 15 | g.73329668T>G | CA393093748 | HCN4 | c.1495A>C (p.Met499Leu) c.277A>C (p.Met93Leu) | |
| 15 | g.73329669G>A | CA491151559 | HCN4 | c.1494C>T (p.Ser498=) c.276C>T (p.Ser92=) | |
| 15 | g.73329669G>C | CA393093749 | HCN4 | c.1494C>G (p.Ser498Arg) c.276C>G (p.Ser92Arg) | ClinVar dbSNP |
| 15 | g.73329669G= | CA2187167500 | HCN4 | c.1494C= (p.Ser498=) c.276C= (p.Ser92=) | |
| 15 | g.73329669G>T | CA393093750 | HCN4 | c.1494C>A (p.Ser498Arg) c.276C>A (p.Ser92Arg) | ClinVar dbSNP |
| 15 | g.73329670C>A | CA393093751 | HCN4 | c.1493G>T (p.Ser498Ile) c.275G>T (p.Ser92Ile) | |
| 15 | g.73329670C>G | CA393093752 | HCN4 | c.1493G>C (p.Ser498Thr) c.275G>C (p.Ser92Thr) | |
| 15 | g.73329670C>T | CA393093753 | HCN4 | c.1493G>A (p.Ser498Asn) c.275G>A (p.Ser92Asn) | |
| 15 | g.73329671T>A | CA393093756 | HCN4 | c.1492A>T (p.Ser498Cys) c.274A>T (p.Ser92Cys) | |
| 15 | g.73329671T>C | CA393093755 | HCN4 | c.1492A>G (p.Ser498Gly) c.274A>G (p.Ser92Gly) | |
| 15 | g.73329671T>G | CA393093754 | HCN4 | c.1492A>C (p.Ser498Arg) c.274A>C (p.Ser92Arg) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73329671T= | CA2187167502 | HCN4 | c.1492A= (p.Ser498=) c.274A= (p.Ser92=) | |
| 15 | g.73329672G>A | CA491151571 | HCN4 | c.1491C>T (p.Leu497=) c.273C>T (p.Leu91=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73329672G>C | CA491151572 | HCN4 | c.1491C>G (p.Leu497=) c.273C>G (p.Leu91=) | |
| 15 | g.73329672G= | CA2187167506 | HCN4 | c.1491C= (p.Leu497=) c.273C= (p.Leu91=) | |
| 15 | g.73329672G>T | CA491151574 | HCN4 | c.1491C>A (p.Leu497=) c.273C>A (p.Leu91=) | |
| 15 | g.73329673A>C | CA393093757 | HCN4 | c.1490T>G (p.Leu497Arg) c.272T>G (p.Leu91Arg) | |
| 15 | g.73329673A>G | CA393093758 | HCN4 | c.1490T>C (p.Leu497Pro) c.272T>C (p.Leu91Pro) | |
| 15 | g.73329673A>T | CA393093759 | HCN4 | c.1490T>A (p.Leu497His) c.272T>A (p.Leu91His) | |
| 15 | g.73329674G>A | CA393093760 | HCN4 | c.1489C>T (p.Leu497Phe) c.271C>T (p.Leu91Phe) | |
| 15 | g.73329674G>C | CA393093761 | HCN4 | c.1489C>G (p.Leu497Val) c.271C>G (p.Leu91Val) | |
| 15 | g.73329674G>T | CA393093762 | HCN4 | c.1489C>A (p.Leu497Ile) c.271C>A (p.Leu91Ile) | |
| 15 | g.73329675C>A | CA393093763 | HCN4 | c.1488G>T (p.Met496Ile) c.270G>T (p.Met90Ile) | |
| 15 | g.73329675C>G | CA393093764 | HCN4 | c.1488G>C (p.Met496Ile) c.270G>C (p.Met90Ile) | |
| 15 | g.73329675C>T | CA393093765 | HCN4 | c.1488G>A (p.Met496Ile) c.270G>A (p.Met90Ile) | |
| 15 | g.73329676A= | CA2187167511 | HCN4 | c.1487T= (p.Met496=) c.269T= (p.Met90=) | |
| 15 | g.73329676A>C | CA393093766 | HCN4 | c.1487T>G (p.Met496Arg) c.269T>G (p.Met90Arg) | |
| 15 | g.73329676A>G | CA393093767 | HCN4 | c.1487T>C (p.Met496Thr) c.269T>C (p.Met90Thr) | dbSNP gnomAD v4 |
| 15 | g.73329676A>T | CA393093768 | HCN4 | c.1487T>A (p.Met496Lys) c.269T>A (p.Met90Lys) | |
| 15 | g.73329677T>A | CA393093770 | HCN4 | c.1486A>T (p.Met496Leu) c.268A>T (p.Met90Leu) | |
| 15 | g.73329677T>C | CA7649286 | HCN4 | c.1486A>G (p.Met496Val) c.268A>G (p.Met90Val) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73329677T>G | CA393093769 | HCN4 | c.1486A>C (p.Met496Leu) c.268A>C (p.Met90Leu) | |
| 15 | g.73329677T= | CA2187167513 | HCN4 | c.1486A= (p.Met496=) c.268A= (p.Met90=) | |
| 15 | g.73329678G>A | CA491151594 | HCN4 | c.1485C>T (p.Thr495=) c.267C>T (p.Thr89=) | |
| 15 | g.73329678G>C | CA491151596 | HCN4 | c.1485C>G (p.Thr495=) c.267C>G (p.Thr89=) | |
| 15 | g.73329678G>T | CA491151592 | HCN4 | c.1485C>A (p.Thr495=) c.267C>A (p.Thr89=) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73329679G>A | CA393093771 | HCN4 | c.1484C>T (p.Thr495Ile) c.266C>T (p.Thr89Ile) | |
| 15 | g.73329679G>C | CA393093772 | HCN4 | c.1484C>G (p.Thr495Ser) c.266C>G (p.Thr89Ser) | |
| 15 | g.73329679G>T | CA393093773 | HCN4 | c.1484C>A (p.Thr495Asn) c.266C>A (p.Thr89Asn) | |
| 15 | g.73329680T>A | CA393093774 | HCN4 | c.1483A>T (p.Thr495Ser) c.265A>T (p.Thr89Ser) | |
| 15 | g.73329680T>C | CA393093775 | HCN4 | c.1483A>G (p.Thr495Ala) c.265A>G (p.Thr89Ala) | gnomAD v4 |
| 15 | g.73329680T>G | CA393093776 | HCN4 | c.1483A>C (p.Thr495Pro) c.265A>C (p.Thr89Pro) | |
| 15 | g.73329681G>A | CA272672050 | HCN4 | c.1482C>T (p.Leu494=) c.264C>T (p.Leu88=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73329681G>C | CA491151603 | HCN4 | c.1482C>G (p.Leu494=) c.264C>G (p.Leu88=) | |
| 15 | g.73329681G= | CA2187167516 | HCN4 | c.1482C= (p.Leu494=) c.264C= (p.Leu88=) | |
| 15 | g.73329681G>T | CA491151605 | HCN4 | c.1482C>A (p.Leu494=) c.264C>A (p.Leu88=) | |
| 15 | g.73329682A>C | CA393093777 | HCN4 | c.1481T>G (p.Leu494Arg) c.263T>G (p.Leu88Arg) | |
| 15 | g.73329682A>G | CA393093778 | HCN4 | c.1481T>C (p.Leu494Pro) c.263T>C (p.Leu88Pro) | |
| 15 | g.73329682A>T | CA393093779 | HCN4 | c.1481T>A (p.Leu494His) c.263T>A (p.Leu88His) | |
| 15 | g.73329683G>A | CA393093780 | HCN4 | c.1480C>T (p.Leu494Phe) c.262C>T (p.Leu88Phe) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73329683G>C | CA393093781 | HCN4 | c.1480C>G (p.Leu494Val) c.262C>G (p.Leu88Val) | |
| 15 | g.73329683G>T | CA393093782 | HCN4 | c.1480C>A (p.Leu494Ile) c.262C>A (p.Leu88Ile) | |
| 15 | g.73329684C>A | CA393093785 | HCN4 | c.1479G>T (p.Trp493Cys) c.261G>T (p.Trp87Cys) | gnomAD v4 |
| 15 | g.73329684C>G | CA393093784 | HCN4 | c.1479G>C (p.Trp493Cys) c.261G>C (p.Trp87Cys) | |
| 15 | g.73329684C>T | CA393093783 | HCN4 | c.1479G>A (p.Trp493Ter) c.261G>A (p.Trp87Ter) | gnomAD v4 |
| 15 | g.73329685C>A | CA393093786 | HCN4 | c.1478G>T (p.Trp493Leu) c.260G>T (p.Trp87Leu) | |
| 15 | g.73329685C>G | CA393093787 | HCN4 | c.1478G>C (p.Trp493Ser) c.260G>C (p.Trp87Ser) | |
| 15 | g.73329685C>T | CA393093788 | HCN4 | c.1478G>A (p.Trp493Ter) c.260G>A (p.Trp87Ter) | gnomAD v4 |
| 15 | g.73329686A>C | CA393093789 | HCN4 | c.1477T>G (p.Trp493Gly) c.259T>G (p.Trp87Gly) | |
| 15 | g.73329686A>G | CA393093790 | HCN4 | c.1477T>C (p.Trp493Arg) c.259T>C (p.Trp87Arg) | |
| 15 | g.73329686A>T | CA393093791 | HCN4 | c.1477T>A (p.Trp493Arg) c.259T>A (p.Trp87Arg) | |
| 15 | g.73329687G>A | CA491151625 | HCN4 | c.1476C>T (p.Val492=) c.258C>T (p.Val86=) | dbSNP |
| 15 | g.73329687G>C | CA491151627 | HCN4 | c.1476C>G (p.Val492=) c.258C>G (p.Val86=) | |
| 15 | g.73329687G= | CA2187167519 | HCN4 | c.1476C= (p.Val492=) c.258C= (p.Val86=) | |
| 15 | g.73329687G>T | CA491151629 | HCN4 | c.1476C>A (p.Val492=) c.258C>A (p.Val86=) | |
| 15 | g.73329688A>C | CA393093792 | HCN4 | c.1475T>G (p.Val492Gly) c.257T>G (p.Val86Gly) | |
| 15 | g.73329688A>G | CA393093793 | HCN4 | c.1475T>C (p.Val492Ala) c.257T>C (p.Val86Ala) | |
| 15 | g.73329688A>T | CA393093794 | HCN4 | c.1475T>A (p.Val492Asp) c.257T>A (p.Val86Asp) | |
| 15 | g.73329689C>A | CA393093795 | HCN4 | c.1474G>T (p.Val492Phe) c.256G>T (p.Val86Phe) | |
| 15 | g.73329689C= | CA2187167522 | HCN4 | c.1474G= (p.Val492=) c.256G= (p.Val86=) | |
| 15 | g.73329689C>G | CA393093796 | HCN4 | c.1474G>C (p.Val492Leu) c.256G>C (p.Val86Leu) | |
| 15 | g.73329689C>T | CA7649287 | HCN4 | c.1474G>A (p.Val492Ile) c.256G>A (p.Val86Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.73329690G>A | CA7649288 | HCN4 | c.1473C>T (p.Asp491=) c.255C>T (p.Asp85=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73329690G>C | CA393093798 | HCN4 | c.1473C>G (p.Asp491Glu) c.255C>G (p.Asp85Glu) | |
| 15 | g.73329690G= | CA2187167528 | HCN4 | c.1473C= (p.Asp491=) c.255C= (p.Asp85=) | |
| 15 | g.73329690G>T | CA393093797 | HCN4 | c.1473C>A (p.Asp491Glu) c.255C>A (p.Asp85Glu) | |
| 15 | g.73329691T>A | CA393093799 | HCN4 | c.1472A>T (p.Asp491Val) c.254A>T (p.Asp85Val) | |
| 15 | g.73329691T>C | CA393093800 | HCN4 | c.1472A>G (p.Asp491Gly) c.254A>G (p.Asp85Gly) | |
| 15 | g.73329691T>G | CA393093801 | HCN4 | c.1472A>C (p.Asp491Ala) c.254A>C (p.Asp85Ala) | |
| 15 | g.73329692C>A | CA393093802 | HCN4 | c.1471G>T (p.Asp491Tyr) c.253G>T (p.Asp85Tyr) | |
| 15 | g.73329692C= | CA2187167535 | HCN4 | c.1471G= (p.Asp491=) c.253G= (p.Asp85=) | |
| 15 | g.73329692C>G | CA393093803 | HCN4 | c.1471G>C (p.Asp491His) c.253G>C (p.Asp85His) | ClinVar dbSNP |
| 15 | g.73329692C>T | CA16614921 | HCN4 | c.1471G>A (p.Asp491Asn) c.253G>A (p.Asp85Asn) | ClinVar dbSNP gnomAD v4 COSMIC |
| 15 | g.73329693G>A | CA7649289 | HCN4 | c.1470C>T (p.Ser490=) c.252C>T (p.Ser84=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73329693G>C | CA491151649 | HCN4 | c.1470C>G (p.Ser490=) c.252C>G (p.Ser84=) | |
| 15 | g.73329693G= | CA2187167541 | HCN4 | c.1470C= (p.Ser490=) c.252C= (p.Ser84=) | |
| 15 | g.73329693G>T | CA491151651 | HCN4 | c.1470C>A (p.Ser490=) c.252C>A (p.Ser84=) | |
| 15 | g.73329694G>A | CA393093806 | HCN4 | c.1469C>T (p.Ser490Phe) c.251C>T (p.Ser84Phe) | |
| 15 | g.73329694G>C | CA393093804 | HCN4 | c.1469C>G (p.Ser490Cys) c.251C>G (p.Ser84Cys) | |
| 15 | g.73329694G>T | CA393093805 | HCN4 | c.1469C>A (p.Ser490Tyr) c.251C>A (p.Ser84Tyr) | |
| 15 | g.73329695A>C | CA393093807 | HCN4 | c.1468T>G (p.Ser490Ala) c.250T>G (p.Ser84Ala) | |
| 15 | g.73329695A>G | CA393093808 | HCN4 | c.1468T>C (p.Ser490Pro) c.250T>C (p.Ser84Pro) | |
| 15 | g.73329695A>T | CA393093810 | HCN4 | c.1468T>A (p.Ser490Thr) c.250T>A (p.Ser84Thr) | |
| 15 | g.73329696C>A | CA393093812 | HCN4 | c.1467G>T (p.Met489Ile) c.249G>T (p.Met83Ile) | |
| 15 | g.73329696C= | CA2187167544 | HCN4 | c.1467G= (p.Met489=) c.249G= (p.Met83=) | |
| 15 | g.73329696C>G | CA393093814 | HCN4 | c.1467G>C (p.Met489Ile) c.249G>C (p.Met83Ile) | |
| 15 | g.73329696C>T | CA7649290 | HCN4 | c.1467G>A (p.Met489Ile) c.249G>A (p.Met83Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73329697A>C | CA393093817 | HCN4 | c.1466T>G (p.Met489Arg) c.248T>G (p.Met83Arg) | |
| 15 | g.73329697A>G | CA393093821 | HCN4 | c.1466T>C (p.Met489Thr) c.248T>C (p.Met83Thr) | gnomAD v4 |
| 15 | g.73329697A>T | CA393093819 | HCN4 | c.1466T>A (p.Met489Lys) c.248T>A (p.Met83Lys) | |
| 15 | g.73329698T>A | CA393093823 | HCN4 | c.1465A>T (p.Met489Leu) c.247A>T (p.Met83Leu) | |
| 15 | g.73329698T>C | CA393093825 | HCN4 | c.1465A>G (p.Met489Val) c.247A>G (p.Met83Val) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73329698T>G | CA393093827 | HCN4 | c.1465A>C (p.Met489Leu) c.247A>C (p.Met83Leu) | |
| 15 | g.73329698T= | CA2187167548 | HCN4 | c.1465A= (p.Met489=) c.247A= (p.Met83=) | |
| 15 | g.73329699G>A | CA491151671 | HCN4 | c.1464C>T (p.Gly488=) c.246C>T (p.Gly82=) | |
| 15 | g.73329699G>C | CA491151669 | HCN4 | c.1464C>G (p.Gly488=) c.246C>G (p.Gly82=) | |
| 15 | g.73329699G>T | CA491151668 | HCN4 | c.1464C>A (p.Gly488=) c.246C>A (p.Gly82=) | |
| 15 | g.73329700C>A | CA393093829 | HCN4 | c.1463G>T (p.Gly488Val) c.245G>T (p.Gly82Val) | |
| 15 | g.73329700C>G | CA393093831 | HCN4 | c.1463G>C (p.Gly488Ala) c.245G>C (p.Gly82Ala) | |
| 15 | g.73329700C>T | CA393093833 | HCN4 | c.1463G>A (p.Gly488Asp) c.245G>A (p.Gly82Asp) | gnomAD v4 |
| 15 | g.73329701C>A | CA393093835 | HCN4 | c.1462G>T (p.Gly488Cys) c.244G>T (p.Gly82Cys) | |
| 15 | g.73329701C= | CA2187167554 | HCN4 | c.1462G= (p.Gly488=) c.244G= (p.Gly82=) | |
| 15 | g.73329701C>G | CA393093836 | HCN4 | c.1462G>C (p.Gly488Arg) c.244G>C (p.Gly82Arg) | |
| 15 | g.73329701C>T | CA10604722 | HCN4 | c.1462G>A (p.Gly488Ser) c.244G>A (p.Gly82Ser) | ClinVar dbSNP |
| 15 | g.73329702C>A | CA491151679 | HCN4 | c.1461G>T (p.Val487=) c.243G>T (p.Val81=) | |
| 15 | g.73329702C>G | CA491151681 | HCN4 | c.1461G>C (p.Val487=) c.243G>C (p.Val81=) | |
| 15 | g.73329702C>T | CA491151683 | HCN4 | c.1461G>A (p.Val487=) c.243G>A (p.Val81=) | gnomAD v4 |
| 15 | g.73329703A>C | CA393093840 | HCN4 | c.1460T>G (p.Val487Gly) c.242T>G (p.Val81Gly) | |
| 15 | g.73329703A>G | CA393093842 | HCN4 | c.1460T>C (p.Val487Ala) c.242T>C (p.Val81Ala) | |
| 15 | g.73329703A>T | CA393093843 | HCN4 | c.1460T>A (p.Val487Glu) c.242T>A (p.Val81Glu) | |
| 15 | g.73329704C>A | CA393093845 | HCN4 | c.1459G>T (p.Val487Leu) c.241G>T (p.Val81Leu) | |
| 15 | g.73329704C= | CA2187167560 | HCN4 | c.1459G= (p.Val487=) c.241G= (p.Val81=) | |
| 15 | g.73329704C>G | CA393093848 | HCN4 | c.1459G>C (p.Val487Leu) c.241G>C (p.Val81Leu) | |
| 15 | g.73329704C>T | CA234114 | HCN4 | c.1459G>A (p.Val487Met) c.241G>A (p.Val81Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |