Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.73323448G>A | CA393088486 | HCN4 | c.2645C>T (p.Pro882Leu) c.1427C>T (p.Pro476Leu) | gnomAD v4 |
15 | g.73323448G>C | CA393088487 | HCN4 | c.2645C>G (p.Pro882Arg) c.1427C>G (p.Pro476Arg) | |
15 | g.73323448G>T | CA393088485 | HCN4 | c.2645C>A (p.Pro882Gln) c.1427C>A (p.Pro476Gln) | gnomAD v4 |
15 | g.73323449G>A | CA393088488 | HCN4 | c.2644C>T (p.Pro882Ser) c.1426C>T (p.Pro476Ser) | |
15 | g.73323449G>C | CA393088489 | HCN4 | c.2644C>G (p.Pro882Ala) c.1426C>G (p.Pro476Ala) | |
15 | g.73323449G>T | CA393088490 | HCN4 | c.2644C>A (p.Pro882Thr) c.1426C>A (p.Pro476Thr) | COSMIC |
15 | g.73323450G>A | CA491478660 | HCN4 | c.2643C>T (p.Ser881=) c.1425C>T (p.Ser475=) | dbSNP gnomAD v2 |
15 | g.73323450G>C | CA491478661 | HCN4 | c.2643C>G (p.Ser881=) c.1425C>G (p.Ser475=) | |
15 | g.73323450G= | CA2187188320 | HCN4 | c.2643C= (p.Ser881=) c.1425C= (p.Ser475=) | |
15 | g.73323450G>T | CA491478662 | HCN4 | c.2643C>A (p.Ser881=) c.1425C>A (p.Ser475=) | |
15 | g.73323451G>A | CA393088491 | HCN4 | c.2642C>T (p.Ser881Phe) c.1424C>T (p.Ser475Phe) | ClinVar dbSNP gnomAD v4 |
15 | g.73323451G>C | CA393088492 | HCN4 | c.2642C>G (p.Ser881Cys) c.1424C>G (p.Ser475Cys) | |
15 | g.73323451G>T | CA393088493 | HCN4 | c.2642C>A (p.Ser881Tyr) c.1424C>A (p.Ser475Tyr) | gnomAD v4 |
15 | g.73323452A= | CA2187188322 | HCN4 | c.2641T= (p.Ser881=) c.1423T= (p.Ser475=) | |
15 | g.73323452A>C | CA393088494 | HCN4 | c.2641T>G (p.Ser881Ala) c.1423T>G (p.Ser475Ala) | |
15 | g.73323452A>G | CA7648983 | HCN4 | c.2641T>C (p.Ser881Pro) c.1423T>C (p.Ser475Pro) | dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73323452A>T | CA393088495 | HCN4 | c.2641T>A (p.Ser881Thr) c.1423T>A (p.Ser475Thr) | |
15 | g.73323453G>A | CA491478674 | HCN4 | c.2640C>T (p.Ser880=) c.1422C>T (p.Ser474=) | |
15 | g.73323453G>C | CA491478676 | HCN4 | c.2640C>G (p.Ser880=) c.1422C>G (p.Ser474=) | |
15 | g.73323453G>T | CA491478677 | HCN4 | c.2640C>A (p.Ser880=) c.1422C>A (p.Ser474=) | gnomAD v4 |
15 | g.73323454G>A | CA393088496 | HCN4 | c.2639C>T (p.Ser880Phe) c.1421C>T (p.Ser474Phe) | gnomAD v4 |
15 | g.73323454G>C | CA393088497 | HCN4 | c.2639C>G (p.Ser880Cys) c.1421C>G (p.Ser474Cys) | |
15 | g.73323454G>T | CA393088498 | HCN4 | c.2639C>A (p.Ser880Tyr) c.1421C>A (p.Ser474Tyr) | gnomAD v4 |
15 | g.73323455A= | CA2187188324 | HCN4 | c.2638T= (p.Ser880=) c.1420T= (p.Ser474=) | |
15 | g.73323455A>C | CA393088501 | HCN4 | c.2638T>G (p.Ser880Ala) c.1420T>G (p.Ser474Ala) | dbSNP gnomAD v3 gnomAD v4 |
15 | g.73323455A>G | CA393088499 | HCN4 | c.2638T>C (p.Ser880Pro) c.1420T>C (p.Ser474Pro) | gnomAD v4 |
15 | g.73323455A>T | CA393088500 | HCN4 | c.2638T>A (p.Ser880Thr) c.1420T>A (p.Ser474Thr) | gnomAD v4 |
15 | g.73323456G>A | CA7648985 | HCN4 | c.2637C>T (p.Ser879=) c.1419C>T (p.Ser473=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73323456G>C | CA7648984 | HCN4 | c.2637C>G (p.Ser879Arg) c.1419C>G (p.Ser473Arg) | dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73323456G= | CA2187188327 | HCN4 | c.2637C= (p.Ser879=) c.1419C= (p.Ser473=) | |
15 | g.73323456G>T | CA393088502 | HCN4 | c.2637C>A (p.Ser879Arg) c.1419C>A (p.Ser473Arg) | gnomAD v4 |
15 | g.73323457C>A | CA393088503 | HCN4 | c.2636G>T (p.Ser879Ile) c.1418G>T (p.Ser473Ile) | |
15 | g.73323457C= | CA2187188336 | HCN4 | c.2636G= (p.Ser879=) c.1418G= (p.Ser473=) | |
15 | g.73323457C>G | CA393088504 | HCN4 | c.2636G>C (p.Ser879Thr) c.1418G>C (p.Ser473Thr) | ClinVar dbSNP gnomAD v4 |
15 | g.73323457C>T | CA393088505 | HCN4 | c.2636G>A (p.Ser879Asn) c.1418G>A (p.Ser473Asn) | dbSNP gnomAD v2 gnomAD v4 |
15 | g.73323458T>A | CA393088506 | HCN4 | c.2635A>T (p.Ser879Cys) c.1417A>T (p.Ser473Cys) | |
15 | g.73323458T>C | CA393088507 | HCN4 | c.2635A>G (p.Ser879Gly) c.1417A>G (p.Ser473Gly) | |
15 | g.73323458T>G | CA393088508 | HCN4 | c.2635A>C (p.Ser879Arg) c.1417A>C (p.Ser473Arg) | |
15 | g.73323459G>A | CA491478688 | HCN4 | c.2634C>T (p.Ser878=) c.1416C>T (p.Ser472=) | |
15 | g.73323459G>C | CA7648986 | HCN4 | c.2634C>G (p.Ser878=) c.1416C>G (p.Ser472=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73323459G= | CA2187188341 | HCN4 | c.2634C= (p.Ser878=) c.1416C= (p.Ser472=) | |
15 | g.73323459G>T | CA491478691 | HCN4 | c.2634C>A (p.Ser878=) c.1416C>A (p.Ser472=) | gnomAD v4 |
15 | g.73323460G>A | CA393088511 | HCN4 | c.2633C>T (p.Ser878Phe) c.1415C>T (p.Ser472Phe) | gnomAD v4 |
15 | g.73323460G>C | CA393088510 | HCN4 | c.2633C>G (p.Ser878Cys) c.1415C>G (p.Ser472Cys) | |
15 | g.73323460G>T | CA393088509 | HCN4 | c.2633C>A (p.Ser878Tyr) c.1415C>A (p.Ser472Tyr) | |
15 | g.73323461A>C | CA393088512 | HCN4 | c.2632T>G (p.Ser878Ala) c.1414T>G (p.Ser472Ala) | |
15 | g.73323461A>G | CA393088514 | HCN4 | c.2632T>C (p.Ser878Pro) c.1414T>C (p.Ser472Pro) | |
15 | g.73323461A>T | CA393088513 | HCN4 | c.2632T>A (p.Ser878Thr) c.1414T>A (p.Ser472Thr) | |
15 | g.73323462T>A | CA491478697 | HCN4 | c.2631A>T (p.Ser877=) c.1413A>T (p.Ser471=) | |
15 | g.73323462T>C | CA491478700 | HCN4 | c.2631A>G (p.Ser877=) c.1413A>G (p.Ser471=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
15 | g.73323462T>G | CA491478701 | HCN4 | c.2631A>C (p.Ser877=) c.1413A>C (p.Ser471=) | |
15 | g.73323462T= | CA2187188344 | HCN4 | c.2631A= (p.Ser877=) c.1413A= (p.Ser471=) | |
15 | g.73323463G>A | CA393088515 | HCN4 | c.2630C>T (p.Ser877Leu) c.1412C>T (p.Ser471Leu) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323463G>C | CA393088516 | HCN4 | c.2630C>G (p.Ser877Ter) c.1412C>G (p.Ser471Ter) | |
15 | g.73323463G= | CA2187188349 | HCN4 | c.2630C= (p.Ser877=) c.1412C= (p.Ser471=) | |
15 | g.73323463G>T | CA393088517 | HCN4 | c.2630C>A (p.Ser877Ter) c.1412C>A (p.Ser471Ter) | gnomAD v4 COSMIC |
15 | g.73323464A>C | CA393088518 | HCN4 | c.2629T>G (p.Ser877Ala) c.1411T>G (p.Ser471Ala) | |
15 | g.73323464A>G | CA393088519 | HCN4 | c.2629T>C (p.Ser877Pro) c.1411T>C (p.Ser471Pro) | |
15 | g.73323464A>T | CA393088520 | HCN4 | c.2629T>A (p.Ser877Thr) c.1411T>A (p.Ser471Thr) | |
15 | g.73323465G>A | CA491478706 | HCN4 | c.2628C>T (p.Pro876=) c.1410C>T (p.Pro470=) | ClinVar dbSNP gnomAD v4 |
15 | g.73323465G>C | CA491478707 | HCN4 | c.2628C>G (p.Pro876=) c.1410C>G (p.Pro470=) | gnomAD v4 |
15 | g.73323465G>T | CA491478708 | HCN4 | c.2628C>A (p.Pro876=) c.1410C>A (p.Pro470=) | gnomAD v4 |
15 | g.73323466G>A | CA393088521 | HCN4 | c.2627C>T (p.Pro876Leu) c.1409C>T (p.Pro470Leu) | dbSNP gnomAD v4 |
15 | g.73323466G>C | CA393088522 | HCN4 | c.2627C>G (p.Pro876Arg) c.1409C>G (p.Pro470Arg) | |
15 | g.73323466G= | CA2187188354 | HCN4 | c.2627C= (p.Pro876=) c.1409C= (p.Pro470=) | |
15 | g.73323466G>T | CA393088523 | HCN4 | c.2627C>A (p.Pro876His) c.1409C>A (p.Pro470His) | |
15 | g.73323467G>A | CA393088524 | HCN4 | c.2626C>T (p.Pro876Ser) c.1408C>T (p.Pro470Ser) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
15 | g.73323467G>C | CA393088525 | HCN4 | c.2626C>G (p.Pro876Ala) c.1408C>G (p.Pro470Ala) | |
15 | g.73323467G= | CA2187188359 | HCN4 | c.2626C= (p.Pro876=) c.1408C= (p.Pro470=) | |
15 | g.73323467G>T | CA393088526 | HCN4 | c.2626C>A (p.Pro876Thr) c.1408C>A (p.Pro470Thr) | |
15 | g.73323468C>A | CA491478714 | HCN4 | c.2625G>T (p.Leu875=) c.1407G>T (p.Leu469=) | |
15 | g.73323468C>G | CA491478715 | HCN4 | c.2625G>C (p.Leu875=) c.1407G>C (p.Leu469=) | |
15 | g.73323468C>T | CA491478716 | HCN4 | c.2625G>A (p.Leu875=) c.1407G>A (p.Leu469=) | gnomAD v4 |
15 | g.73323469A>C | CA393088527 | HCN4 | c.2624T>G (p.Leu875Arg) c.1406T>G (p.Leu469Arg) | |
15 | g.73323469A>G | CA393088529 | HCN4 | c.2624T>C (p.Leu875Pro) c.1406T>C (p.Leu469Pro) | |
15 | g.73323469A>T | CA393088528 | HCN4 | c.2624T>A (p.Leu875Gln) c.1406T>A (p.Leu469Gln) | |
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.73323477del | CA2840286485 | HCN4 | c.2618del (p.Pro873HisfsTer27) c.1400del (p.Pro467HisfsTer27) | |
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 |
15 | g.73323484C>A | CA393088556 | HCN4 | c.2609G>T (p.Gly870Val) c.1391G>T (p.Gly464Val) | gnomAD v4 |
15 | g.73323484C= | CA2187188393 | HCN4 | c.2609G= (p.Gly870=) c.1391G= (p.Gly464=) | |
15 | g.73323484C>G | CA393088557 | HCN4 | c.2609G>C (p.Gly870Ala) c.1391G>C (p.Gly464Ala) | |
15 | g.73323484C>T | CA7648990 | HCN4 | c.2609G>A (p.Gly870Glu) c.1391G>A (p.Gly464Glu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73323485C>A | CA393088560 | HCN4 | c.2608G>T (p.Gly870Ter) c.1390G>T (p.Gly464Ter) | |
15 | g.73323485C= | CA2187188395 | HCN4 | c.2608G= (p.Gly870=) c.1390G= (p.Gly464=) | |
15 | g.73323485C>G | CA393088558 | HCN4 | c.2608G>C (p.Gly870Arg) c.1390G>C (p.Gly464Arg) | |
15 | g.73323485C>T | CA393088559 | HCN4 | c.2608G>A (p.Gly870Arg) c.1390G>A (p.Gly464Arg) | dbSNP gnomAD v3 gnomAD v4 |
15 | g.73323486A>C | CA491478757 | HCN4 | c.2607T>G (p.Ala869=) c.1389T>G (p.Ala463=) | |
15 | g.73323486A>G | CA491478756 | HCN4 | c.2607T>C (p.Ala869=) c.1389T>C (p.Ala463=) | ClinVar |
15 | g.73323486A>T | CA491478755 | HCN4 | c.2607T>A (p.Ala869=) c.1389T>A (p.Ala463=) | gnomAD v4 |
15 | g.73323487G>A | CA7648991 | HCN4 | c.2606C>T (p.Ala869Val) c.1388C>T (p.Ala463Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323487G>C | CA393088561 | HCN4 | c.2606C>G (p.Ala869Gly) c.1388C>G (p.Ala463Gly) | |
15 | g.73323487G= | CA2187188399 | HCN4 | c.2606C= (p.Ala869=) c.1388C= (p.Ala463=) | |
15 | g.73323487G>T | CA393088562 | HCN4 | c.2606C>A (p.Ala869Asp) c.1388C>A (p.Ala463Asp) | |
15 | g.73323488C>A | CA393088563 | HCN4 | c.2605G>T (p.Ala869Ser) c.1387G>T (p.Ala463Ser) | |
15 | g.73323488C= | CA2187188405 | HCN4 | c.2605G= (p.Ala869=) c.1387G= (p.Ala463=) | |
15 | g.73323488C>G | CA7648992 | HCN4 | c.2605G>C (p.Ala869Pro) c.1387G>C (p.Ala463Pro) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323488C>T | CA7648993 | HCN4 | c.2605G>A (p.Ala869Thr) c.1387G>A (p.Ala463Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323489G>A | CA7648995 | HCN4 | c.2604C>T (p.Pro868=) c.1386C>T (p.Pro462=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323489G>C | CA7648994 | HCN4 | c.2604C>G (p.Pro868=) c.1386C>G (p.Pro462=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323489G= | CA2187188415 | HCN4 | c.2604C= (p.Pro868=) c.1386C= (p.Pro462=) | |
15 | g.73323489G>T | CA491478768 | HCN4 | c.2604C>A (p.Pro868=) c.1386C>A (p.Pro462=) | ClinVar dbSNP gnomAD v4 |
15 | g.73323493del | CA2575783834 | HCN4 | c.2604del (p.Ala869LeufsTer3) c.1386del (p.Ala463LeufsTer3) | gnomAD v4 |
15 | g.73323490G>A | CA393088564 | HCN4 | c.2603C>T (p.Pro868Leu) c.1385C>T (p.Pro462Leu) | |
15 | g.73323490G>C | CA393088565 | HCN4 | c.2603C>G (p.Pro868Arg) c.1385C>G (p.Pro462Arg) | |
15 | g.73323490G>T | CA393088566 | HCN4 | c.2603C>A (p.Pro868His) c.1385C>A (p.Pro462His) | gnomAD v4 |
15 | g.73323491G>A | CA393088567 | HCN4 | c.2602C>T (p.Pro868Ser) c.1384C>T (p.Pro462Ser) | dbSNP gnomAD v4 |
15 | g.73323491G>C | CA393088568 | HCN4 | c.2602C>G (p.Pro868Ala) c.1384C>G (p.Pro462Ala) | |
15 | g.73323491G= | CA2187188419 | HCN4 | c.2602C= (p.Pro868=) c.1384C= (p.Pro462=) | |
15 | g.73323491G>T | CA393088569 | HCN4 | c.2602C>A (p.Pro868Thr) c.1384C>A (p.Pro462Thr) | |
15 | g.73323492G>A | CA491478778 | HCN4 | c.2601C>T (p.Ala867=) c.1383C>T (p.Ala461=) | gnomAD v3 gnomAD v4 |
15 | g.73323492G>C | CA491478779 | HCN4 | c.2601C>G (p.Ala867=) c.1383C>G (p.Ala461=) | |
15 | g.73323492G= | CA2187188422 | HCN4 | c.2601C= (p.Ala867=) c.1383C= (p.Ala461=) | |
15 | g.73323492G>T | CA203633 | HCN4 | c.2601C>A (p.Ala867=) c.1383C>A (p.Ala461=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323493G>A | CA393088570 | HCN4 | c.2600C>T (p.Ala867Val) c.1382C>T (p.Ala461Val) | |
15 | g.73323493G>C | CA393088571 | HCN4 | c.2600C>G (p.Ala867Gly) c.1382C>G (p.Ala461Gly) | |
15 | g.73323493G>T | CA393088572 | HCN4 | c.2600C>A (p.Ala867Asp) c.1382C>A (p.Ala461Asp) | ClinVar |
15 | g.73323494C>A | CA393088573 | HCN4 | c.2599G>T (p.Ala867Ser) c.1381G>T (p.Ala461Ser) | |
15 | g.73323494C>G | CA393088574 | HCN4 | c.2599G>C (p.Ala867Pro) c.1381G>C (p.Ala461Pro) | |
15 | g.73323494C>T | CA393088575 | HCN4 | c.2599G>A (p.Ala867Thr) c.1381G>A (p.Ala461Thr) | |
15 | g.73323495A>C | CA491478783 | HCN4 | c.2598T>G (p.Ser866=) c.1380T>G (p.Ser460=) | |
15 | g.73323495A>G | CA491478785 | HCN4 | c.2598T>C (p.Ser866=) c.1380T>C (p.Ser460=) | gnomAD v4 |
15 | g.73323495A>T | CA491478788 | HCN4 | c.2598T>A (p.Ser866=) c.1380T>A (p.Ser460=) | |
15 | g.73323496G>A | CA393088578 | HCN4 | c.2597C>T (p.Ser866Phe) c.1379C>T (p.Ser460Phe) | |
15 | g.73323496G>C | CA393088577 | HCN4 | c.2597C>G (p.Ser866Cys) c.1379C>G (p.Ser460Cys) | |
15 | g.73323496G>T | CA393088576 | HCN4 | c.2597C>A (p.Ser866Tyr) c.1379C>A (p.Ser460Tyr) | |
15 | g.73323497A>C | CA393088579 | HCN4 | c.2596T>G (p.Ser866Ala) c.1378T>G (p.Ser460Ala) | |
15 | g.73323497A>G | CA393088580 | HCN4 | c.2596T>C (p.Ser866Pro) c.1378T>C (p.Ser460Pro) | |
15 | g.73323497A>T | CA393088581 | HCN4 | c.2596T>A (p.Ser866Thr) c.1378T>A (p.Ser460Thr) | |
15 | g.73323498G>A | CA272664566 | HCN4 | c.2595C>T (p.Phe865=) c.1377C>T (p.Phe459=) | ClinVar dbSNP COSMIC |
15 | g.73323498G>C | CA393088582 | HCN4 | c.2595C>G (p.Phe865Leu) c.1377C>G (p.Phe459Leu) | |
15 | g.73323498G= | CA2187188426 | HCN4 | c.2595C= (p.Phe865=) c.1377C= (p.Phe459=) | |
15 | g.73323498G>T | CA393088583 | HCN4 | c.2595C>A (p.Phe865Leu) c.1377C>A (p.Phe459Leu) | |
15 | g.73323499A>C | CA393088584 | HCN4 | c.2594T>G (p.Phe865Cys) c.1376T>G (p.Phe459Cys) | |
15 | g.73323499A>G | CA393088585 | HCN4 | c.2594T>C (p.Phe865Ser) c.1376T>C (p.Phe459Ser) | |
15 | g.73323499A>T | CA393088586 | HCN4 | c.2594T>A (p.Phe865Tyr) c.1376T>A (p.Phe459Tyr) | |
15 | g.73323500A>C | CA393088587 | HCN4 | c.2593T>G (p.Phe865Val) c.1375T>G (p.Phe459Val) | |
15 | g.73323500A>G | CA393088588 | HCN4 | c.2593T>C (p.Phe865Leu) c.1375T>C (p.Phe459Leu) | |
15 | g.73323500A>T | CA393088589 | HCN4 | c.2593T>A (p.Phe865Ile) c.1375T>A (p.Phe459Ile) | |
15 | g.73323501T>A | CA491478791 | HCN4 | c.2592A>T (p.Gly864=) c.1374A>T (p.Gly458=) | |
15 | g.73323501T>C | CA491478793 | HCN4 | c.2592A>G (p.Gly864=) c.1374A>G (p.Gly458=) | |
15 | g.73323501T>G | CA491478794 | HCN4 | c.2592A>C (p.Gly864=) c.1374A>C (p.Gly458=) | |
15 | g.73323501_73323502delinsAA | CA272664570 | HCN4 | c.2591_2592delinsTT (p.Gly864Val) c.1373_1374delinsTT (p.Gly458Val) | dbSNP |
15 | g.73323501_73323502delinsTC | CA2187188430 | HCN4 | c.2591_2592delinsGA (p.Gly864=) c.1373_1374delinsGA (p.Gly458=) | |
15 | g.73323502C>A | CA393088590 | HCN4 | c.2591G>T (p.Gly864Val) c.1373G>T (p.Gly458Val) | |
15 | g.73323502C= | CA2187188432 | HCN4 | c.2591G= (p.Gly864=) c.1373G= (p.Gly458=) | |
15 | g.73323502C>G | CA393088591 | HCN4 | c.2591G>C (p.Gly864Ala) c.1373G>C (p.Gly458Ala) | |
15 | g.73323502C>T | CA393088592 | HCN4 | c.2591G>A (p.Gly864Glu) c.1373G>A (p.Gly458Glu) | dbSNP |
15 | g.73323503C>A | CA393088595 | HCN4 | c.2590G>T (p.Gly864Ter) c.1372G>T (p.Gly458Ter) | |
15 | g.73323503C= | CA2187188435 | HCN4 | c.2590G= (p.Gly864=) c.1372G= (p.Gly458=) | |
15 | g.73323503C>G | CA393088594 | HCN4 | c.2590G>C (p.Gly864Arg) c.1372G>C (p.Gly458Arg) | |
15 | g.73323503C>T | CA393088593 | HCN4 | c.2590G>A (p.Gly864Arg) c.1372G>A (p.Gly458Arg) | dbSNP gnomAD v3 gnomAD v4 |
15 | g.73323504A>C | CA491478799 | HCN4 | c.2589T>G (p.Ala863=) c.1371T>G (p.Ala457=) | |
15 | g.73323504A>G | CA491478800 | HCN4 | c.2589T>C (p.Ala863=) c.1371T>C (p.Ala457=) | |
15 | g.73323504A>T | CA491478801 | HCN4 | c.2589T>A (p.Ala863=) c.1371T>A (p.Ala457=) | |
15 | g.73323505G>A | CA393088596 | HCN4 | c.2588C>T (p.Ala863Val) c.1370C>T (p.Ala457Val) | gnomAD v4 |
15 | g.73323505G>C | CA393088597 | HCN4 | c.2588C>G (p.Ala863Gly) c.1370C>G (p.Ala457Gly) | |
15 | g.73323505G>T | CA393088598 | HCN4 | c.2588C>A (p.Ala863Asp) c.1370C>A (p.Ala457Asp) | gnomAD v4 |
15 | g.73323506C>A | CA272664581 | HCN4 | c.2587G>T (p.Ala863Ser) c.1369G>T (p.Ala457Ser) | ClinVar dbSNP |
15 | g.73323506C= | CA2187188443 | HCN4 | c.2587G= (p.Ala863=) c.1369G= (p.Ala457=) | |
15 | g.73323506C>G | CA393088599 | HCN4 | c.2587G>C (p.Ala863Pro) c.1369G>C (p.Ala457Pro) | |
15 | g.73323506C>T | CA7648996 | HCN4 | c.2587G>A (p.Ala863Thr) c.1369G>A (p.Ala457Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323507C>A | CA491478814 | HCN4 | c.2586G>T (p.Leu862=) c.1368G>T (p.Leu456=) | |
15 | g.73323507C>G | CA491478816 | HCN4 | c.2586G>C (p.Leu862=) c.1368G>C (p.Leu456=) | |
15 | g.73323507C>T | CA491478813 | HCN4 | c.2586G>A (p.Leu862=) c.1368G>A (p.Leu456=) | |
15 | g.73323508A= | CA2187188453 | HCN4 | c.2585T= (p.Leu862=) c.1367T= (p.Leu456=) | |
15 | g.73323508A>C | CA393088600 | HCN4 | c.2585T>G (p.Leu862Arg) c.1367T>G (p.Leu456Arg) | |
15 | g.73323508A>G | CA393088601 | HCN4 | c.2585T>C (p.Leu862Pro) c.1367T>C (p.Leu456Pro) | dbSNP gnomAD v2 gnomAD v4 |
15 | g.73323508A>T | CA393088602 | HCN4 | c.2585T>A (p.Leu862Gln) c.1367T>A (p.Leu456Gln) | |
15 | g.73323509G>A | CA491478827 | HCN4 | c.2584C>T (p.Leu862=) c.1366C>T (p.Leu456=) | |
15 | g.73323509G>C | CA393088603 | HCN4 | c.2584C>G (p.Leu862Val) c.1366C>G (p.Leu456Val) | |
15 | g.73323509G>T | CA393088604 | HCN4 | c.2584C>A (p.Leu862Met) c.1366C>A (p.Leu456Met) | |
15 | g.73323510C>A | CA393088605 | HCN4 | c.2583G>T (p.Gln861His) c.1365G>T (p.Gln455His) | |
15 | g.73323510C>G | CA393088606 | HCN4 | c.2583G>C (p.Gln861His) c.1365G>C (p.Gln455His) | |
15 | g.73323510C>T | CA491478829 | HCN4 | c.2583G>A (p.Gln861=) c.1365G>A (p.Gln455=) | |
15 | g.73323511T>A | CA393088609 | HCN4 | c.2582A>T (p.Gln861Leu) c.1364A>T (p.Gln455Leu) | |
15 | g.73323511T>C | CA393088608 | HCN4 | c.2582A>G (p.Gln861Arg) c.1364A>G (p.Gln455Arg) | gnomAD v4 |
15 | g.73323511T>G | CA393088607 | HCN4 | c.2582A>C (p.Gln861Pro) c.1364A>C (p.Gln455Pro) | |
15 | g.73323512G>A | CA393088610 | HCN4 | c.2581C>T (p.Gln861Ter) c.1363C>T (p.Gln455Ter) | |
15 | g.73323512G>C | CA393088611 | HCN4 | c.2581C>G (p.Gln861Glu) c.1363C>G (p.Gln455Glu) | |
15 | g.73323512G>T | CA393088612 | HCN4 | c.2581C>A (p.Gln861Lys) c.1363C>A (p.Gln455Lys) | |
15 | g.73323513T>A | CA393088613 | HCN4 | c.2580A>T (p.Gln860His) c.1362A>T (p.Gln454His) | |
15 | g.73323513T>C | CA7648997 | HCN4 | c.2580A>G (p.Gln860=) c.1362A>G (p.Gln454=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323513T>G | CA393088614 | HCN4 | c.2580A>C (p.Gln860His) c.1362A>C (p.Gln454His) | |
15 | g.73323513T= | CA2187188455 | HCN4 | c.2580A= (p.Gln860=) c.1362A= (p.Gln454=) | |
15 | g.73323514T>A | CA393088615 | HCN4 | c.2579A>T (p.Gln860Leu) c.1361A>T (p.Gln454Leu) | |
15 | g.73323514T>C | CA393088616 | HCN4 | c.2579A>G (p.Gln860Arg) c.1361A>G (p.Gln454Arg) | |
15 | g.73323514T>G | CA393088617 | HCN4 | c.2579A>C (p.Gln860Pro) c.1361A>C (p.Gln454Pro) | |
15 | g.73323515G>A | CA393088618 | HCN4 | c.2578C>T (p.Gln860Ter) c.1360C>T (p.Gln454Ter) | |
15 | g.73323515G>C | CA393088619 | HCN4 | c.2578C>G (p.Gln860Glu) c.1360C>G (p.Gln454Glu) | |
15 | g.73323515G>T | CA393088620 | HCN4 | c.2578C>A (p.Gln860Lys) c.1360C>A (p.Gln454Lys) | |
15 | g.73323516G>A | CA491478837 | HCN4 | c.2577C>T (p.Ile859=) c.1359C>T (p.Ile453=) | |
15 | g.73323516G>C | CA393088621 | HCN4 | c.2577C>G (p.Ile859Met) c.1359C>G (p.Ile453Met) | gnomAD v4 COSMIC |
15 | g.73323516G>T | CA491478839 | HCN4 | c.2577C>A (p.Ile859=) c.1359C>A (p.Ile453=) | |
15 | g.73323517A>C | CA393088623 | HCN4 | c.2576T>G (p.Ile859Ser) c.1358T>G (p.Ile453Ser) | |
15 | g.73323517A>G | CA393088624 | HCN4 | c.2576T>C (p.Ile859Thr) c.1358T>C (p.Ile453Thr) | |
15 | g.73323517A>T | CA393088622 | HCN4 | c.2576T>A (p.Ile859Asn) c.1358T>A (p.Ile453Asn) | |
15 | g.73323518T>A | CA393088625 | HCN4 | c.2575A>T (p.Ile859Phe) c.1357A>T (p.Ile453Phe) | |
15 | g.73323518T>C | CA393088627 | HCN4 | c.2575A>G (p.Ile859Val) c.1357A>G (p.Ile453Val) | |
15 | g.73323518T>G | CA393088626 | HCN4 | c.2575A>C (p.Ile859Leu) c.1357A>C (p.Ile453Leu) | |
15 | g.73323519G>A | CA491478845 | HCN4 | c.2574C>T (p.His858=) c.1356C>T (p.His452=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323519G>C | CA393088628 | HCN4 | c.2574C>G (p.His858Gln) c.1356C>G (p.His452Gln) | |
15 | g.73323519G= | CA2187188458 | HCN4 | c.2574C= (p.His858=) c.1356C= (p.His452=) | |
15 | g.73323519G>T | CA393088629 | HCN4 | c.2574C>A (p.His858Gln) c.1356C>A (p.His452Gln) | |
15 | g.73323520T>A | CA393088630 | HCN4 | c.2573A>T (p.His858Leu) c.1355A>T (p.His452Leu) | |
15 | g.73323520T>C | CA393088631 | HCN4 | c.2573A>G (p.His858Arg) c.1355A>G (p.His452Arg) | gnomAD v4 |
15 | g.73323520T>G | CA393088632 | HCN4 | c.2573A>C (p.His858Pro) c.1355A>C (p.His452Pro) | |
15 | g.73323521G>A | CA393088633 | HCN4 | c.2572C>T (p.His858Tyr) c.1354C>T (p.His452Tyr) | gnomAD v4 |
15 | g.73323521G>C | CA393088634 | HCN4 | c.2572C>G (p.His858Asp) c.1354C>G (p.His452Asp) | |
15 | g.73323521G>T | CA393088635 | HCN4 | c.2572C>A (p.His858Asn) c.1354C>A (p.His452Asn) | gnomAD v4 |
15 | g.73323522G>A | CA491478855 | HCN4 | c.2571C>T (p.Phe857=) c.1353C>T (p.Phe451=) | |
15 | g.73323522G>C | CA7648998 | HCN4 | c.2571C>G (p.Phe857Leu) c.1353C>G (p.Phe451Leu) | ClinVar dbSNP ExAC gnomAD v4 |
15 | g.73323522G= | CA2187188461 | HCN4 | c.2571C= (p.Phe857=) c.1353C= (p.Phe451=) | |
15 | g.73323522G>T | CA393088636 | HCN4 | c.2571C>A (p.Phe857Leu) c.1353C>A (p.Phe451Leu) | |
15 | g.73323523A>C | CA393088639 | HCN4 | c.2570T>G (p.Phe857Cys) c.1352T>G (p.Phe451Cys) | |
15 | g.73323523A>G | CA393088638 | HCN4 | c.2570T>C (p.Phe857Ser) c.1352T>C (p.Phe451Ser) | gnomAD v4 |
15 | g.73323523A>T | CA393088637 | HCN4 | c.2570T>A (p.Phe857Tyr) c.1352T>A (p.Phe451Tyr) | |
15 | g.73323524A>C | CA393088640 | HCN4 | c.2569T>G (p.Phe857Val) c.1351T>G (p.Phe451Val) | |
15 | g.73323524A>G | CA393088641 | HCN4 | c.2569T>C (p.Phe857Leu) c.1351T>C (p.Phe451Leu) | |
15 | g.73323524A>T | CA393088642 | HCN4 | c.2569T>A (p.Phe857Ile) c.1351T>A (p.Phe451Ile) | |
15 | g.73323525G>A | CA491478860 | HCN4 | c.2568C>T (p.Ser856=) c.1350C>T (p.Ser450=) | gnomAD v4 |
15 | g.73323525G>C | CA491478861 | HCN4 | c.2568C>G (p.Ser856=) c.1350C>G (p.Ser450=) | |
15 | g.73323525G>T | CA491478863 | HCN4 | c.2568C>A (p.Ser856=) c.1350C>A (p.Ser450=) | |
15 | g.73323526G>A | CA393088643 | HCN4 | c.2567C>T (p.Ser856Phe) c.1349C>T (p.Ser450Phe) | ClinVar gnomAD v4 COSMIC |
15 | g.73323526G>C | CA393088644 | HCN4 | c.2567C>G (p.Ser856Cys) c.1349C>G (p.Ser450Cys) | |
15 | g.73323526G>T | CA393088645 | HCN4 | c.2567C>A (p.Ser856Tyr) c.1349C>A (p.Ser450Tyr) | |
15 | g.73323527A>C | CA393088646 | HCN4 | c.2566T>G (p.Ser856Ala) c.1348T>G (p.Ser450Ala) | gnomAD v4 |
15 | g.73323527A>G | CA393088647 | HCN4 | c.2566T>C (p.Ser856Pro) c.1348T>C (p.Ser450Pro) | |
15 | g.73323527A>T | CA393088648 | HCN4 | c.2566T>A (p.Ser856Thr) c.1348T>A (p.Ser450Thr) | |
15 | g.73323528G>A | CA491478879 | HCN4 | c.2565C>T (p.Ser855=) c.1347C>T (p.Ser449=) | |
15 | g.73323528G>C | CA491478878 | HCN4 | c.2565C>G (p.Ser855=) c.1347C>G (p.Ser449=) | gnomAD v4 |
15 | g.73323528G>T | CA491478877 | HCN4 | c.2565C>A (p.Ser855=) c.1347C>A (p.Ser449=) | gnomAD v4 |
15 | g.73323529G>A | CA393088649 | HCN4 | c.2564C>T (p.Ser855Phe) c.1346C>T (p.Ser449Phe) | COSMIC |
15 | g.73323529G>C | CA393088650 | HCN4 | c.2564C>G (p.Ser855Cys) c.1346C>G (p.Ser449Cys) | |
15 | g.73323529G>T | CA393088651 | HCN4 | c.2564C>A (p.Ser855Tyr) c.1346C>A (p.Ser449Tyr) | gnomAD v4 COSMIC |
15 | g.73323530A= | CA2187188465 | HCN4 | c.2563T= (p.Ser855=) c.1345T= (p.Ser449=) | |
15 | g.73323530A>C | CA393088653 | HCN4 | c.2563T>G (p.Ser855Ala) c.1345T>G (p.Ser449Ala) | |
15 | g.73323530A>G | CA7648999 | HCN4 | c.2563T>C (p.Ser855Pro) c.1345T>C (p.Ser449Pro) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323530A>T | CA393088652 | HCN4 | c.2563T>A (p.Ser855Thr) c.1345T>A (p.Ser449Thr) | |
15 | g.73323531T>A | CA491478182 | HCN4 | c.2562A>T (p.Ser854=) c.1344A>T (p.Ser448=) | |
15 | g.73323531T>C | CA491478183 | HCN4 | c.2562A>G (p.Ser854=) c.1344A>G (p.Ser448=) | |
15 | g.73323531T>G | CA491478184 | HCN4 | c.2562A>C (p.Ser854=) c.1344A>C (p.Ser448=) | |
15 | g.73323532G>A | CA393088654 | HCN4 | c.2561C>T (p.Ser854Leu) c.1343C>T (p.Ser448Leu) | COSMIC |
15 | g.73323532G>C | CA393088655 | HCN4 | c.2561C>G (p.Ser854Ter) c.1343C>G (p.Ser448Ter) | |
15 | g.73323532G>T | CA393088656 | HCN4 | c.2561C>A (p.Ser854Ter) c.1343C>A (p.Ser448Ter) | gnomAD v4 |
15 | g.73323533A= | CA2187188469 | HCN4 | c.2560T= (p.Ser854=) c.1342T= (p.Ser448=) | |
15 | g.73323533A>C | CA393088657 | HCN4 | c.2560T>G (p.Ser854Ala) c.1342T>G (p.Ser448Ala) | |
15 | g.73323533A>G | CA7649000 | HCN4 | c.2560T>C (p.Ser854Pro) c.1342T>C (p.Ser448Pro) | ClinVar dbSNP ExAC gnomAD v2 |
15 | g.73323533A>T | CA393088658 | HCN4 | c.2560T>A (p.Ser854Thr) c.1342T>A (p.Ser448Thr) | |
15 | g.73323534A>C | CA491478187 | HCN4 | c.2559T>G (p.Ser853=) c.1341T>G (p.Ser447=) | |
15 | g.73323534A>G | CA491478188 | HCN4 | c.2559T>C (p.Ser853=) c.1341T>C (p.Ser447=) | |
15 | g.73323534A>T | CA491478190 | HCN4 | c.2559T>A (p.Ser853=) c.1341T>A (p.Ser447=) | |
15 | g.73323535G>A | CA393088659 | HCN4 | c.2558C>T (p.Ser853Phe) c.1340C>T (p.Ser447Phe) | gnomAD v4 |
15 | g.73323535G>C | CA393088660 | HCN4 | c.2558C>G (p.Ser853Cys) c.1340C>G (p.Ser447Cys) | |
15 | g.73323535G>T | CA393088661 | HCN4 | c.2558C>A (p.Ser853Tyr) c.1340C>A (p.Ser447Tyr) | |
15 | g.73323536A>C | CA393088662 | HCN4 | c.2557T>G (p.Ser853Ala) c.1339T>G (p.Ser447Ala) | |
15 | g.73323536A>G | CA393088663 | HCN4 | c.2557T>C (p.Ser853Pro) c.1339T>C (p.Ser447Pro) | gnomAD v4 |
15 | g.73323536A>T | CA393088664 | HCN4 | c.2557T>A (p.Ser853Thr) c.1339T>A (p.Ser447Thr) | |
15 | g.73323537C>A | CA491478191 | HCN4 | c.2556G>T (p.Pro852=) c.1338G>T (p.Pro446=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323537C= | CA2187188476 | HCN4 | c.2556G= (p.Pro852=) c.1338G= (p.Pro446=) | |
15 | g.73323537C>G | CA491478192 | HCN4 | c.2556G>C (p.Pro852=) c.1338G>C (p.Pro446=) | |
15 | g.73323537C>T | CA148386 | HCN4 | c.2556G>A (p.Pro852=) c.1338G>A (p.Pro446=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323538G>A | CA7649001 | HCN4 | c.2555C>T (p.Pro852Leu) c.1337C>T (p.Pro446Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
15 | g.73323538G>C | CA393088666 | HCN4 | c.2555C>G (p.Pro852Arg) c.1337C>G (p.Pro446Arg) | |
15 | g.73323538G= | CA2187188480 | HCN4 | c.2555C= (p.Pro852=) c.1337C= (p.Pro446=) | |
15 | g.73323538G>T | CA393088665 | HCN4 | c.2555C>A (p.Pro852Gln) c.1337C>A (p.Pro446Gln) | dbSNP |
15 | g.73323539G>A | CA393088667 | HCN4 | c.2554C>T (p.Pro852Ser) c.1336C>T (p.Pro446Ser) | |
15 | g.73323539G>C | CA393088668 | HCN4 | c.2554C>G (p.Pro852Ala) c.1336C>G (p.Pro446Ala) | gnomAD v4 |
15 | g.73323539G>T | CA393088669 | HCN4 | c.2554C>A (p.Pro852Thr) c.1336C>A (p.Pro446Thr) | |
15 | g.73323539_73323540insCGT | CA2629370568 | HCN4 | c.2553_2554insACG (p.Thr851_Pro852insThr) c.1335_1336insACG (p.Thr445_Pro446insThr) | gnomAD v4 |
15 | g.73323540T>A | CA491478197 | HCN4 | c.2553A>T (p.Thr851=) c.1335A>T (p.Thr445=) | |
15 | g.73323540T>C | CA247659 | HCN4 | c.2553A>G (p.Thr851=) c.1335A>G (p.Thr445=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73323540T>G | CA491478196 | HCN4 | c.2553A>C (p.Thr851=) c.1335A>C (p.Thr445=) | |
15 | g.73323540T= | CA2187188487 | HCN4 | c.2553A= (p.Thr851=) c.1335A= (p.Thr445=) | |
15 | g.73323541G>A | CA393088670 | HCN4 | c.2552C>T (p.Thr851Ile) c.1334C>T (p.Thr445Ile) | |
15 | g.73323541G>C | CA393088671 | HCN4 | c.2552C>G (p.Thr851Arg) c.1334C>G (p.Thr445Arg) | |
15 | g.73323541G>T | CA393088672 | HCN4 | c.2552C>A (p.Thr851Lys) c.1334C>A (p.Thr445Lys) | |
15 | g.73323542T>A | CA393088673 | HCN4 | c.2551A>T (p.Thr851Ser) c.1333A>T (p.Thr445Ser) | |
15 | g.73323542T>C | CA393088674 | HCN4 | c.2551A>G (p.Thr851Ala) c.1333A>G (p.Thr445Ala) | ClinVar dbSNP |
15 | g.73323542T>G | CA393088675 | HCN4 | c.2551A>C (p.Thr851Pro) c.1333A>C (p.Thr445Pro) | ClinVar |
15 | g.73323542T= | CA2187188496 | HCN4 | c.2551A= (p.Thr851=) c.1333A= (p.Thr445=) | |
15 | g.73323543G>A | CA491478198 | HCN4 | c.2550C>T (p.Asp850=) c.1332C>T (p.Asp444=) | dbSNP |
15 | g.73323543G>C | CA393088676 | HCN4 | c.2550C>G (p.Asp850Glu) c.1332C>G (p.Asp444Glu) | |
15 | g.73323543G= | CA2187188499 | HCN4 | c.2550C= (p.Asp850=) c.1332C= (p.Asp444=) | |
15 | g.73323543G>T | CA393088677 | HCN4 | c.2550C>A (p.Asp850Glu) c.1332C>A (p.Asp444Glu) | gnomAD v4 |
15 | g.73323544T>A | CA393088680 | HCN4 | c.2549A>T (p.Asp850Val) c.1331A>T (p.Asp444Val) | |
15 | g.73323544T>C | CA393088679 | HCN4 | c.2549A>G (p.Asp850Gly) c.1331A>G (p.Asp444Gly) | dbSNP gnomAD v2 gnomAD v4 |
15 | g.73323544T>G | CA393088678 | HCN4 | c.2549A>C (p.Asp850Ala) c.1331A>C (p.Asp444Ala) | |
15 | g.73323544T= | CA2187188503 | HCN4 | c.2549A= (p.Asp850=) c.1331A= (p.Asp444=) | |
15 | g.73323545C>A | CA393088681 | HCN4 | c.2548G>T (p.Asp850Tyr) c.1330G>T (p.Asp444Tyr) | |
15 | g.73323545C= | CA2187188506 | HCN4 | c.2548G= (p.Asp850=) c.1330G= (p.Asp444=) | |
15 | g.73323545C>G | CA393088682 | HCN4 | c.2548G>C (p.Asp850His) c.1330G>C (p.Asp444His) | |
15 | g.73323545C>T | CA272664617 | HCN4 | c.2548G>A (p.Asp850Asn) c.1330G>A (p.Asp444Asn) | dbSNP gnomAD v3 gnomAD v4 |
15 | g.73323546C>A | CA491478201 | HCN4 | c.2547G>T (p.Val849=) c.1329G>T (p.Val443=) | |
15 | g.73323546C= | CA2187188511 | HCN4 | c.2547G= (p.Val849=) c.1329G= (p.Val443=) | |
15 | g.73323546C>G | CA491478200 | HCN4 | c.2547G>C (p.Val849=) c.1329G>C (p.Val443=) | |
15 | g.73323546C>T | CA272664618 | HCN4 | c.2547G>A (p.Val849=) c.1329G>A (p.Val443=) | dbSNP gnomAD v2 gnomAD v4 |
15 | g.73323547A>C | CA393088684 | HCN4 | c.2546T>G (p.Val849Gly) c.1328T>G (p.Val443Gly) | |
15 | g.73323547A>G | CA393088683 | HCN4 | c.2546T>C (p.Val849Ala) c.1328T>C (p.Val443Ala) | |
15 | g.73323547A>T | CA393088685 | HCN4 | c.2546T>A (p.Val849Glu) c.1328T>A (p.Val443Glu) | |
15 | g.73323547_73323548delinsAC | CA2187188513 | HCN4 | c.2545_2546delinsGT (p.Val849=) c.1327_1328delinsGT (p.Val443=) | |
15 | g.73323548C>A | CA236699 | HCN4 | c.2545G>T (p.Val849Leu) c.1327G>T (p.Val443Leu) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323548C= | CA2187188516 | HCN4 | c.2545G= (p.Val849=) c.1327G= (p.Val443=) | |
15 | g.73323548C>G | CA393088686 | HCN4 | c.2545G>C (p.Val849Leu) c.1327G>C (p.Val443Leu) | |
15 | g.73323548C>T | CA393088687 | HCN4 | c.2545G>A (p.Val849Met) c.1327G>A (p.Val443Met) | dbSNP gnomAD v2 gnomAD v4 |
15 | g.73323549del | CA7649002 | HCN4 | c.2545del (p.Val849TrpfsTer23) c.1327del (p.Val443TrpfsTer23) | dbSNP ExAC gnomAD v2 gnomAD v4 |