Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.73323470G>A | CA491478718 | HCN4 | c.2623C>T (p.Leu875=) c.1405C>T (p.Leu469=) | ClinVar dbSNP gnomAD v2 |
15 | g.73323470G>C | CA393088530 | HCN4 | c.2623C>G (p.Leu875Val) c.1405C>G (p.Leu469Val) | |
15 | g.73323470G= | CA2187188364 | HCN4 | c.2623C= (p.Leu875=) c.1405C= (p.Leu469=) | |
15 | g.73323470G>T | CA393088531 | HCN4 | c.2623C>A (p.Leu875Met) c.1405C>A (p.Leu469Met) | gnomAD v4 |
15 | g.73323471G>A | CA491478719 | HCN4 | c.2622C>T (p.Leu874=) c.1404C>T (p.Leu468=) | |
15 | g.73323471G>C | CA491478720 | HCN4 | c.2622C>G (p.Leu874=) c.1404C>G (p.Leu468=) | |
15 | g.73323471G>T | CA491478721 | HCN4 | c.2622C>A (p.Leu874=) c.1404C>A (p.Leu468=) | ClinVar gnomAD v4 |
15 | g.73323472A>C | CA393088532 | HCN4 | c.2621T>G (p.Leu874Arg) c.1403T>G (p.Leu468Arg) | |
15 | g.73323472A>G | CA393088533 | HCN4 | c.2621T>C (p.Leu874Pro) c.1403T>C (p.Leu468Pro) | |
15 | g.73323472A>T | CA393088534 | HCN4 | c.2621T>A (p.Leu874His) c.1403T>A (p.Leu468His) | |
15 | g.73323473G>A | CA393088535 | HCN4 | c.2620C>T (p.Leu874Phe) c.1402C>T (p.Leu468Phe) | |
15 | g.73323473G>C | CA393088536 | HCN4 | c.2620C>G (p.Leu874Val) c.1402C>G (p.Leu468Val) | |
15 | g.73323473G>T | CA393088537 | HCN4 | c.2620C>A (p.Leu874Ile) c.1402C>A (p.Leu468Ile) | gnomAD v4 |
15 | g.73323474T>A | CA7648987 | HCN4 | c.2619A>T (p.Pro873=) c.1401A>T (p.Pro467=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323474T>C | CA272664527 | HCN4 | c.2619A>G (p.Pro873=) c.1401A>G (p.Pro467=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323474T>G | CA491478725 | HCN4 | c.2619A>C (p.Pro873=) c.1401A>C (p.Pro467=) | dbSNP |
15 | g.73323474T= | CA2187188368 | HCN4 | c.2619A= (p.Pro873=) c.1401A= (p.Pro467=) | |
15 | g.73323475G>A | CA393088539 | HCN4 | c.2618C>T (p.Pro873Leu) c.1400C>T (p.Pro467Leu) | gnomAD v4 COSMIC |
15 | g.73323475G>C | CA393088540 | HCN4 | c.2618C>G (p.Pro873Arg) c.1400C>G (p.Pro467Arg) | |
15 | g.73323475G>T | CA393088538 | HCN4 | c.2618C>A (p.Pro873Gln) c.1400C>A (p.Pro467Gln) | |
15 | g.73323476G>A | CA393088541 | HCN4 | c.2617C>T (p.Pro873Ser) c.1399C>T (p.Pro467Ser) | |
15 | g.73323476G>C | CA393088542 | HCN4 | c.2617C>G (p.Pro873Ala) c.1399C>G (p.Pro467Ala) | COSMIC |
15 | g.73323476G>T | CA393088543 | HCN4 | c.2617C>A (p.Pro873Thr) c.1399C>A (p.Pro467Thr) | gnomAD v4 |
15 | g.73323477G>A | CA491478729 | HCN4 | c.2616C>T (p.Ser872=) c.1398C>T (p.Ser466=) | dbSNP gnomAD v2 gnomAD v4 |
15 | g.73323477G>C | CA7648988 | HCN4 | c.2616C>G (p.Ser872Arg) c.1398C>G (p.Ser466Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73323477G= | CA2187188375 | HCN4 | c.2616C= (p.Ser872=) c.1398C= (p.Ser466=) | |
15 | g.73323477G>T | CA393088544 | HCN4 | c.2616C>A (p.Ser872Arg) c.1398C>A (p.Ser466Arg) | gnomAD v4 |
15 | g.73323478C>A | CA393088545 | HCN4 | c.2615G>T (p.Ser872Ile) c.1397G>T (p.Ser466Ile) | |
15 | g.73323478C= | CA2187188383 | HCN4 | c.2615G= (p.Ser872=) c.1397G= (p.Ser466=) | |
15 | g.73323478C>G | CA393088546 | HCN4 | c.2615G>C (p.Ser872Thr) c.1397G>C (p.Ser466Thr) | |
15 | g.73323478C>T | CA393088547 | HCN4 | c.2615G>A (p.Ser872Asn) c.1397G>A (p.Ser466Asn) | ClinVar dbSNP COSMIC |
15 | g.73323479T>A | CA393088548 | HCN4 | c.2614A>T (p.Ser872Cys) c.1396A>T (p.Ser466Cys) | |
15 | g.73323479T>C | CA393088549 | HCN4 | c.2614A>G (p.Ser872Gly) c.1396A>G (p.Ser466Gly) | |
15 | g.73323479T>G | CA393088550 | HCN4 | c.2614A>C (p.Ser872Arg) c.1396A>C (p.Ser466Arg) | |
15 | g.73323480C>A | CA491478735 | HCN4 | c.2613G>T (p.Leu871=) c.1395G>T (p.Leu465=) | gnomAD v4 |
15 | g.73323480C= | CA2187188386 | HCN4 | c.2613G= (p.Leu871=) c.1395G= (p.Leu465=) | |
15 | g.73323480C>G | CA491478737 | HCN4 | c.2613G>C (p.Leu871=) c.1395G>C (p.Leu465=) | |
15 | g.73323480C>T | CA491478739 | HCN4 | c.2613G>A (p.Leu871=) c.1395G>A (p.Leu465=) | |
15 | g.73323481A>C | CA393088553 | HCN4 | c.2612T>G (p.Leu871Arg) c.1394T>G (p.Leu465Arg) | |
15 | g.73323481A>G | CA393088552 | HCN4 | c.2612T>C (p.Leu871Pro) c.1394T>C (p.Leu465Pro) | |
15 | g.73323481A>T | CA393088551 | HCN4 | c.2612T>A (p.Leu871Gln) c.1394T>A (p.Leu465Gln) | |
15 | g.73323482_73323499dup | CA7648989 | HCN4 | c.2595_2612dup (p.Leu871_Ser872insSerAlaProAlaGlyLeu) c.1377_1394dup (p.Leu465_Ser466insSerAlaProAlaGlyLeu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73323482G>A | CA491478741 | HCN4 | c.2611C>T (p.Leu871=) c.1393C>T (p.Leu465=) | COSMIC |
15 | g.73323482G>C | CA393088554 | HCN4 | c.2611C>G (p.Leu871Val) c.1393C>G (p.Leu465Val) | |
15 | g.73323482G= | CA2187188390 | HCN4 | c.2611C= (p.Leu871=) c.1393C= (p.Leu465=) | |
15 | g.73323482G>T | CA393088555 | HCN4 | c.2611C>A (p.Leu871Met) c.1393C>A (p.Leu465Met) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
15 | g.73323483T>A | CA491478745 | HCN4 | c.2610A>T (p.Gly870=) c.1392A>T (p.Gly464=) | |
15 | g.73323483T>C | CA491478746 | HCN4 | c.2610A>G (p.Gly870=) c.1392A>G (p.Gly464=) | gnomAD v4 |
15 | g.73323483T>G | CA491478748 | HCN4 | c.2610A>C (p.Gly870=) c.1392A>C (p.Gly464=) | |
15 | g.73323489_73323506del | CA2739269578 | HCN4 | c.2593_2610del (p.Phe865_Gly870del) c.1375_1392del (p.Phe459_Gly464del) | ClinVar |