Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.73329603C>A | CA491151463 | HCN4 | c.1560G>T (p.Leu520=) c.342G>T (p.Leu114=) | |
15 | g.73329603C= | CA2187167419 | HCN4 | c.1560G= (p.Leu520=) c.342G= (p.Leu114=) | |
15 | g.73329603C>G | CA491151464 | HCN4 | c.1560G>C (p.Leu520=) c.342G>C (p.Leu114=) | |
15 | g.73329603C>T | CA7649282 | HCN4 | c.1560G>A (p.Leu520=) c.342G>A (p.Leu114=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
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=) |