Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.73332179C>A | CA393094344 | HCN4 | c.1323G>T (p.Met441Ile) c.105G>T (p.Met35Ile) | |
15 | g.73332179C>G | CA393094345 | HCN4 | c.1323G>C (p.Met441Ile) c.105G>C (p.Met35Ile) | |
15 | g.73332179C>T | CA393094346 | HCN4 | c.1323G>A (p.Met441Ile) c.105G>A (p.Met35Ile) | gnomAD v4 COSMIC |
15 | g.73332180A>C | CA393094347 | HCN4 | c.1322T>G (p.Met441Arg) c.104T>G (p.Met35Arg) | |
15 | g.73332180A>G | CA393094348 | HCN4 | c.1322T>C (p.Met441Thr) c.104T>C (p.Met35Thr) | |
15 | g.73332180A>T | CA393094349 | HCN4 | c.1322T>A (p.Met441Lys) c.104T>A (p.Met35Lys) | |
15 | g.73332181T>A | CA393094350 | HCN4 | c.1321A>T (p.Met441Leu) c.103A>T (p.Met35Leu) | |
15 | g.73332181T>C | CA7649326 | HCN4 | c.1321A>G (p.Met441Val) c.103A>G (p.Met35Val) | dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73332181T>G | CA393094351 | HCN4 | c.1321A>C (p.Met441Leu) c.103A>C (p.Met35Leu) | |
15 | g.73332181T= | CA2187169779 | HCN4 | c.1321A= (p.Met441=) c.103A= (p.Met35=) | |
15 | g.73332182G>A | CA491152542 | HCN4 | c.1320C>T (p.Pro440=) c.102C>T (p.Pro34=) | |
15 | g.73332182G>C | CA491152543 | HCN4 | c.1320C>G (p.Pro440=) c.102C>G (p.Pro34=) | |
15 | g.73332182G>T | CA491152544 | HCN4 | c.1320C>A (p.Pro440=) c.102C>A (p.Pro34=) | |
15 | g.73332183G>A | CA393094353 | HCN4 | c.1319C>T (p.Pro440Leu) c.101C>T (p.Pro34Leu) | gnomAD v4 |
15 | g.73332183G>C | CA393094354 | HCN4 | c.1319C>G (p.Pro440Arg) c.101C>G (p.Pro34Arg) | |
15 | g.73332183G>T | CA393094352 | HCN4 | c.1319C>A (p.Pro440His) c.101C>A (p.Pro34His) | |
15 | g.73332184G>A | CA393094355 | HCN4 | c.1318C>T (p.Pro440Ser) c.100C>T (p.Pro34Ser) | dbSNP gnomAD v2 gnomAD v4 COSMIC |
15 | g.73332184G>C | CA393094356 | HCN4 | c.1318C>G (p.Pro440Ala) c.100C>G (p.Pro34Ala) | |
15 | g.73332184G= | CA2187169781 | HCN4 | c.1318C= (p.Pro440=) c.100C= (p.Pro34=) | |
15 | g.73332184G>T | CA393094357 | HCN4 | c.1318C>A (p.Pro440Thr) c.100C>A (p.Pro34Thr) | |
15 | g.73332185T>A | CA491152547 | HCN4 | c.1317A>T (p.Val439=) c.99A>T (p.Val33=) | |
15 | g.73332185T>C | CA491152546 | HCN4 | c.1317A>G (p.Val439=) c.99A>G (p.Val33=) | |
15 | g.73332185T>G | CA491152545 | HCN4 | c.1317A>C (p.Val439=) c.99A>C (p.Val33=) | |
15 | g.73332186A>C | CA393094358 | HCN4 | c.1316T>G (p.Val439Gly) c.98T>G (p.Val33Gly) | |
15 | g.73332186A>G | CA393094359 | HCN4 | c.1316T>C (p.Val439Ala) c.98T>C (p.Val33Ala) | gnomAD v4 |
15 | g.73332186A>T | CA393094360 | HCN4 | c.1316T>A (p.Val439Glu) c.98T>A (p.Val33Glu) | |
15 | g.73332187C>A | CA393094361 | HCN4 | c.1315G>T (p.Val439Leu) c.97G>T (p.Val33Leu) | |
15 | g.73332187C= | CA2187169785 | HCN4 | c.1315G= (p.Val439=) c.97G= (p.Val33=) | |
15 | g.73332187C>G | CA7649327 | HCN4 | c.1315G>C (p.Val439Leu) c.97G>C (p.Val33Leu) | ClinVar dbSNP ExAC |
15 | g.73332187C>T | CA393094362 | HCN4 | c.1315G>A (p.Val439Ile) c.97G>A (p.Val33Ile) | ClinVar |
15 | g.73332188C>A | CA491152550 | HCN4 | c.1314G>T (p.Leu438=) c.96G>T (p.Leu32=) | |
15 | g.73332188C>G | CA491152549 | HCN4 | c.1314G>C (p.Leu438=) c.96G>C (p.Leu32=) | |
15 | g.73332188C>T | CA491152548 | HCN4 | c.1314G>A (p.Leu438=) c.96G>A (p.Leu32=) | gnomAD v4 |
15 | g.73332189A>C | CA393094363 | HCN4 | c.1313T>G (p.Leu438Arg) c.95T>G (p.Leu32Arg) | |
15 | g.73332189A>G | CA393094364 | HCN4 | c.1313T>C (p.Leu438Pro) c.95T>C (p.Leu32Pro) | |
15 | g.73332189A>T | CA393094365 | HCN4 | c.1313T>A (p.Leu438Gln) c.95T>A (p.Leu32Gln) | |
15 | g.73332190G>A | CA491152551 | HCN4 | c.1312C>T (p.Leu438=) c.94C>T (p.Leu32=) | ClinVar dbSNP |
15 | g.73332190G>C | CA393094366 | HCN4 | c.1312C>G (p.Leu438Val) c.94C>G (p.Leu32Val) | |
15 | g.73332190G= | CA2187169789 | HCN4 | c.1312C= (p.Leu438=) c.94C= (p.Leu32=) | |
15 | g.73332190G>T | CA393094367 | HCN4 | c.1312C>A (p.Leu438Met) c.94C>A (p.Leu32Met) | |
15 | g.73332191G>A | CA491152552 | HCN4 | c.1311C>T (p.Phe437=) c.93C>T (p.Phe31=) | |
15 | g.73332191G>C | CA393094369 | HCN4 | c.1311C>G (p.Phe437Leu) c.93C>G (p.Phe31Leu) | |
15 | g.73332191G>T | CA393094368 | HCN4 | c.1311C>A (p.Phe437Leu) c.93C>A (p.Phe31Leu) | |
15 | g.73332192A>C | CA393094370 | HCN4 | c.1310T>G (p.Phe437Cys) c.92T>G (p.Phe31Cys) | |
15 | g.73332192A>G | CA393094371 | HCN4 | c.1310T>C (p.Phe437Ser) c.92T>C (p.Phe31Ser) | |
15 | g.73332192A>T | CA393094372 | HCN4 | c.1310T>A (p.Phe437Tyr) c.92T>A (p.Phe31Tyr) | |
15 | g.73332193A>C | CA393094373 | HCN4 | c.1309T>G (p.Phe437Val) c.91T>G (p.Phe31Val) | |
15 | g.73332193A>G | CA393094374 | HCN4 | c.1309T>C (p.Phe437Leu) c.91T>C (p.Phe31Leu) | |
15 | g.73332193A>T | CA393094375 | HCN4 | c.1309T>A (p.Phe437Ile) c.91T>A (p.Phe31Ile) | |
15 | g.73332194C>A | CA393094377 | HCN4 | c.1308G>T (p.Gln436His) c.90G>T (p.Gln30His) | ClinVar dbSNP COSMIC |
15 | g.73332194C= | CA2187169791 | HCN4 | c.1308G= (p.Gln436=) c.90G= (p.Gln30=) | |
15 | g.73332194C>G | CA393094376 | HCN4 | c.1308G>C (p.Gln436His) c.90G>C (p.Gln30His) | |
15 | g.73332194C>T | CA491152553 | HCN4 | c.1308G>A (p.Gln436=) c.90G>A (p.Gln30=) | ClinVar dbSNP |
15 | g.73332195T>A | CA393094378 | HCN4 | c.1307A>T (p.Gln436Leu) c.89A>T (p.Gln30Leu) | |
15 | g.73332195T>C | CA393094379 | HCN4 | c.1307A>G (p.Gln436Arg) c.89A>G (p.Gln30Arg) | |
15 | g.73332195T>G | CA393094380 | HCN4 | c.1307A>C (p.Gln436Pro) c.89A>C (p.Gln30Pro) | |
15 | g.73332196G>A | CA393094381 | HCN4 | c.1306C>T (p.Gln436Ter) c.88C>T (p.Gln30Ter) | |
15 | g.73332196G>C | CA393094382 | HCN4 | c.1306C>G (p.Gln436Glu) c.88C>G (p.Gln30Glu) | |
15 | g.73332196G>T | CA393094383 | HCN4 | c.1306C>A (p.Gln436Lys) c.88C>A (p.Gln30Lys) | |
15 | g.73332197C>A | CA491152555 | HCN4 | c.1305G>T (p.Leu435=) c.87G>T (p.Leu29=) | |
15 | g.73332197C>G | CA491152556 | HCN4 | c.1305G>C (p.Leu435=) c.87G>C (p.Leu29=) | |
15 | g.73332197C>T | CA491152557 | HCN4 | c.1305G>A (p.Leu435=) c.87G>A (p.Leu29=) | |
15 | g.73332198A= | CA2187169796 | HCN4 | c.1304T= (p.Leu435=) c.86T= (p.Leu29=) | |
15 | g.73332198A>C | CA393094385 | HCN4 | c.1304T>G (p.Leu435Arg) c.86T>G (p.Leu29Arg) | |
15 | g.73332198A>G | CA7649328 | HCN4 | c.1304T>C (p.Leu435Pro) c.86T>C (p.Leu29Pro) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73332198A>T | CA393094384 | HCN4 | c.1304T>A (p.Leu435Gln) c.86T>A (p.Leu29Gln) | |
15 | g.73332199G>A | CA7649329 | HCN4 | c.1303C>T (p.Leu435=) c.85C>T (p.Leu29=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73332199G>C | CA393094386 | HCN4 | c.1303C>G (p.Leu435Val) c.85C>G (p.Leu29Val) | |
15 | g.73332199G= | CA2187169798 | HCN4 | c.1303C= (p.Leu435=) c.85C= (p.Leu29=) | |
15 | g.73332199G>T | CA393094387 | HCN4 | c.1303C>A (p.Leu435Met) c.85C>A (p.Leu29Met) | |
15 | g.73332200G>A | CA491152559 | HCN4 | c.1302C>T (p.Cys434=) c.84C>T (p.Cys28=) | |
15 | g.73332200G>C | CA393094388 | HCN4 | c.1302C>G (p.Cys434Trp) c.84C>G (p.Cys28Trp) | |
15 | g.73332200G>T | CA393094389 | HCN4 | c.1302C>A (p.Cys434Ter) c.84C>A (p.Cys28Ter) | |
15 | g.73332201C>A | CA393094392 | HCN4 | c.1301G>T (p.Cys434Phe) c.83G>T (p.Cys28Phe) | |
15 | g.73332201C>G | CA393094391 | HCN4 | c.1301G>C (p.Cys434Ser) c.83G>C (p.Cys28Ser) | |
15 | g.73332201C>T | CA393094390 | HCN4 | c.1301G>A (p.Cys434Tyr) c.83G>A (p.Cys28Tyr) | |
15 | g.73332202A>C | CA393094393 | HCN4 | c.1300T>G (p.Cys434Gly) c.82T>G (p.Cys28Gly) | |
15 | g.73332202A>G | CA393094394 | HCN4 | c.1300T>C (p.Cys434Arg) c.82T>C (p.Cys28Arg) | |
15 | g.73332202A>T | CA393094395 | HCN4 | c.1300T>A (p.Cys434Ser) c.82T>A (p.Cys28Ser) | |
15 | g.73332203G>A | CA491152560 | HCN4 | c.1299C>T (p.Gly433=) c.81C>T (p.Gly27=) | |
15 | g.73332203G>C | CA491152561 | HCN4 | c.1299C>G (p.Gly433=) c.81C>G (p.Gly27=) | |
15 | g.73332203G>T | CA491152563 | HCN4 | c.1299C>A (p.Gly433=) c.81C>A (p.Gly27=) | |
15 | g.73332204C>A | CA393094396 | HCN4 | c.1298G>T (p.Gly433Val) c.80G>T (p.Gly27Val) | |
15 | g.73332204C>G | CA393094397 | HCN4 | c.1298G>C (p.Gly433Ala) c.80G>C (p.Gly27Ala) | |
15 | g.73332204C>T | CA393094398 | HCN4 | c.1298G>A (p.Gly433Asp) c.80G>A (p.Gly27Asp) | |
15 | g.73332205C>A | CA393094399 | HCN4 | c.1297G>T (p.Gly433Cys) c.79G>T (p.Gly27Cys) | |
15 | g.73332205C= | CA2187169804 | HCN4 | c.1297G= (p.Gly433=) c.79G= (p.Gly27=) | |
15 | g.73332205C>G | CA393094400 | HCN4 | c.1297G>C (p.Gly433Arg) c.79G>C (p.Gly27Arg) | |
15 | g.73332205C>T | CA7649330 | HCN4 | c.1297G>A (p.Gly433Ser) c.79G>A (p.Gly27Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73332206G>A | CA491152567 | HCN4 | c.1296C>T (p.Asp432=) c.78C>T (p.Asp26=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
15 | g.73332206G>C | CA393094401 | HCN4 | c.1296C>G (p.Asp432Glu) c.78C>G (p.Asp26Glu) | |
15 | g.73332206G= | CA2187169810 | HCN4 | c.1296C= (p.Asp432=) c.78C= (p.Asp26=) | |
15 | g.73332206G>T | CA393094402 | HCN4 | c.1296C>A (p.Asp432Glu) c.78C>A (p.Asp26Glu) | |
15 | g.73332207T>A | CA393094403 | HCN4 | c.1295A>T (p.Asp432Val) c.77A>T (p.Asp26Val) | |
15 | g.73332207T>C | CA393094404 | HCN4 | c.1295A>G (p.Asp432Gly) c.77A>G (p.Asp26Gly) | |
15 | g.73332207T>G | CA393094405 | HCN4 | c.1295A>C (p.Asp432Ala) c.77A>C (p.Asp26Ala) | |
15 | g.73332208C>A | CA393094406 | HCN4 | c.1294G>T (p.Asp432Tyr) c.76G>T (p.Asp26Tyr) | |
15 | g.73332208C>G | CA393094407 | HCN4 | c.1294G>C (p.Asp432His) c.76G>C (p.Asp26His) | |
15 | g.73332208C>T | CA393094408 | HCN4 | c.1294G>A (p.Asp432Asn) c.76G>A (p.Asp26Asn) | |
15 | g.73332210del | CA2575783969 | HCN4 | c.1294del (p.Asp432ThrfsTer26) c.76del (p.Asp26ThrfsTer26) | |
15 | g.73332209C>A | CA393094409 | HCN4 | c.1293G>T (p.Trp431Cys) c.75G>T (p.Trp25Cys) | |
15 | g.73332209C>G | CA393094410 | HCN4 | c.1293G>C (p.Trp431Cys) c.75G>C (p.Trp25Cys) | |
15 | g.73332209C>T | CA393094411 | HCN4 | c.1293G>A (p.Trp431Ter) c.75G>A (p.Trp25Ter) | |
15 | g.73332210C>A | CA393094412 | HCN4 | c.1292G>T (p.Trp431Leu) c.74G>T (p.Trp25Leu) | |
15 | g.73332210C>G | CA393094414 | HCN4 | c.1292G>C (p.Trp431Ser) c.74G>C (p.Trp25Ser) | |
15 | g.73332210C>T | CA393094413 | HCN4 | c.1292G>A (p.Trp431Ter) c.74G>A (p.Trp25Ter) | gnomAD v4 |
15 | g.73332211A>C | CA393094415 | HCN4 | c.1291T>G (p.Trp431Gly) c.73T>G (p.Trp25Gly) | |
15 | g.73332211A>G | CA393094417 | HCN4 | c.1291T>C (p.Trp431Arg) c.73T>C (p.Trp25Arg) | |
15 | g.73332211A>T | CA393094416 | HCN4 | c.1291T>A (p.Trp431Arg) c.73T>A (p.Trp25Arg) | |
15 | g.73332212G>A | CA272673937 | HCN4 | c.1290C>T (p.His430=) c.72C>T (p.His24=) | ClinVar dbSNP gnomAD v4 |
15 | g.73332212G>C | CA393094418 | HCN4 | c.1290C>G (p.His430Gln) c.72C>G (p.His24Gln) | COSMIC |
15 | g.73332212G= | CA2187169814 | HCN4 | c.1290C= (p.His430=) c.72C= (p.His24=) | |
15 | g.73332212G>T | CA393094419 | HCN4 | c.1290C>A (p.His430Gln) c.72C>A (p.His24Gln) | |
15 | g.73332213T>A | CA393094420 | HCN4 | c.1289A>T (p.His430Leu) c.71A>T (p.His24Leu) | |
15 | g.73332213T>C | CA393094421 | HCN4 | c.1289A>G (p.His430Arg) c.71A>G (p.His24Arg) | |
15 | g.73332213T>G | CA393094422 | HCN4 | c.1289A>C (p.His430Pro) c.71A>C (p.His24Pro) | |
15 | g.73332214G>A | CA393094423 | HCN4 | c.1288C>T (p.His430Tyr) c.70C>T (p.His24Tyr) | |
15 | g.73332214G>C | CA393094424 | HCN4 | c.1288C>G (p.His430Asp) c.70C>G (p.His24Asp) | |
15 | g.73332214G>T | CA393094425 | HCN4 | c.1288C>A (p.His430Asn) c.70C>A (p.His24Asn) | |
15 | g.73332215G>A | CA491152574 | HCN4 | c.1287C>T (p.Cys429=) c.69C>T (p.Cys23=) | |
15 | g.73332215G>C | CA393094426 | HCN4 | c.1287C>G (p.Cys429Trp) c.69C>G (p.Cys23Trp) | |
15 | g.73332215G>T | CA393094427 | HCN4 | c.1287C>A (p.Cys429Ter) c.69C>A (p.Cys23Ter) | |
15 | g.73332216C>A | CA393094430 | HCN4 | c.1286G>T (p.Cys429Phe) c.68G>T (p.Cys23Phe) | |
15 | g.73332216C>G | CA393094428 | HCN4 | c.1286G>C (p.Cys429Ser) c.68G>C (p.Cys23Ser) | |
15 | g.73332216C>T | CA393094429 | HCN4 | c.1286G>A (p.Cys429Tyr) c.68G>A (p.Cys23Tyr) | |
15 | g.73332217A>C | CA393094431 | HCN4 | c.1285T>G (p.Cys429Gly) c.67T>G (p.Cys23Gly) | |
15 | g.73332217A>G | CA393094432 | HCN4 | c.1285T>C (p.Cys429Arg) c.67T>C (p.Cys23Arg) | |
15 | g.73332217A>T | CA393094433 | HCN4 | c.1285T>A (p.Cys429Ser) c.67T>A (p.Cys23Ser) | |
15 | g.73332218G>A | CA7649331 | HCN4 | c.1284C>T (p.Leu428=) c.66C>T (p.Leu22=) | ClinVar dbSNP ExAC gnomAD v2 |
15 | g.73332218G>C | CA491152579 | HCN4 | c.1284C>G (p.Leu428=) c.66C>G (p.Leu22=) | dbSNP gnomAD v2 gnomAD v4 |
15 | g.73332218G= | CA2187169819 | HCN4 | c.1284C= (p.Leu428=) c.66C= (p.Leu22=) | |
15 | g.73332218G>T | CA491152580 | HCN4 | c.1284C>A (p.Leu428=) c.66C>A (p.Leu22=) | |
15 | g.73332219A= | CA2187169821 | HCN4 | c.1283T= (p.Leu428=) c.65T= (p.Leu22=) | |
15 | g.73332219A>C | CA393094434 | HCN4 | c.1283T>G (p.Leu428Arg) c.65T>G (p.Leu22Arg) | |
15 | g.73332219A>G | CA393094435 | HCN4 | c.1283T>C (p.Leu428Pro) c.65T>C (p.Leu22Pro) | dbSNP gnomAD v4 |
15 | g.73332219A>T | CA393094436 | HCN4 | c.1283T>A (p.Leu428His) c.65T>A (p.Leu22His) | |
15 | g.73332220G>A | CA393094437 | HCN4 | c.1282C>T (p.Leu428Phe) c.64C>T (p.Leu22Phe) | |
15 | g.73332220G>C | CA393094438 | HCN4 | c.1282C>G (p.Leu428Val) c.64C>G (p.Leu22Val) | |
15 | g.73332220G>T | CA393094439 | HCN4 | c.1282C>A (p.Leu428Ile) c.64C>A (p.Leu22Ile) | |
15 | g.73332221C>A | CA491152582 | HCN4 | c.1281G>T (p.Leu427=) c.63G>T (p.Leu21=) | ClinVar gnomAD v4 |
15 | g.73332221C>G | CA491152583 | HCN4 | c.1281G>C (p.Leu427=) c.63G>C (p.Leu21=) | |
15 | g.73332221C>T | CA491152584 | HCN4 | c.1281G>A (p.Leu427=) c.63G>A (p.Leu21=) | |
15 | g.73332222A>C | CA393094441 | HCN4 | c.1280T>G (p.Leu427Arg) c.62T>G (p.Leu21Arg) | |
15 | g.73332222A>G | CA393094442 | HCN4 | c.1280T>C (p.Leu427Pro) c.62T>C (p.Leu21Pro) | |
15 | g.73332222A>T | CA393094440 | HCN4 | c.1280T>A (p.Leu427Gln) c.62T>A (p.Leu21Gln) | |
15 | g.73332223G>A | CA491152586 | HCN4 | c.1279C>T (p.Leu427=) c.61C>T (p.Leu21=) | |
15 | g.73332223G>C | CA393094443 | HCN4 | c.1279C>G (p.Leu427Val) c.61C>G (p.Leu21Val) | |
15 | g.73332223G>T | CA393094444 | HCN4 | c.1279C>A (p.Leu427Met) c.61C>A (p.Leu21Met) | |
15 | g.73332224del | CA2629388815 | HCN4 | c.1279del (p.Leu427CysfsTer?) c.61del (p.Leu21CysfsTer?) | gnomAD v4 |
15 | g.73332224G>A | CA491152587 | HCN4 | c.1278C>T (p.Leu426=) c.60C>T (p.Leu20=) | ClinVar COSMIC |
15 | g.73332224G>C | CA7649332 | HCN4 | c.1278C>G (p.Leu426=) c.60C>G (p.Leu20=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73332224G= | CA2187169823 | HCN4 | c.1278C= (p.Leu426=) c.60C= (p.Leu20=) | |
15 | g.73332224G>T | CA491152589 | HCN4 | c.1278C>A (p.Leu426=) c.60C>A (p.Leu20=) | |
15 | g.73332225A>C | CA393094445 | HCN4 | c.1277T>G (p.Leu426Arg) c.59T>G (p.Leu20Arg) | |
15 | g.73332225A>G | CA393094446 | HCN4 | c.1277T>C (p.Leu426Pro) c.59T>C (p.Leu20Pro) | |
15 | g.73332225A>T | CA393094447 | HCN4 | c.1277T>A (p.Leu426His) c.59T>A (p.Leu20His) | |
15 | g.73332226G>A | CA393094448 | HCN4 | c.1276C>T (p.Leu426Phe) c.58C>T (p.Leu20Phe) | |
15 | g.73332226G>C | CA393094449 | HCN4 | c.1276C>G (p.Leu426Val) c.58C>G (p.Leu20Val) | |
15 | g.73332226G>T | CA393094450 | HCN4 | c.1276C>A (p.Leu426Ile) c.58C>A (p.Leu20Ile) | |
15 | g.73332227C>A | CA393094451 | HCN4 | c.1275G>T (p.Met425Ile) c.57G>T (p.Met19Ile) | |
15 | g.73332227C>G | CA393094452 | HCN4 | c.1275G>C (p.Met425Ile) c.57G>C (p.Met19Ile) | |
15 | g.73332227C>T | CA393094453 | HCN4 | c.1275G>A (p.Met425Ile) c.57G>A (p.Met19Ile) | |
15 | g.73332228A>C | CA393094456 | HCN4 | c.1274T>G (p.Met425Arg) c.56T>G (p.Met19Arg) | |
15 | g.73332228A>G | CA393094454 | HCN4 | c.1274T>C (p.Met425Thr) c.56T>C (p.Met19Thr) | gnomAD v4 |
15 | g.73332228A>T | CA393094455 | HCN4 | c.1274T>A (p.Met425Lys) c.56T>A (p.Met19Lys) | |
15 | g.73332229T>A | CA393094457 | HCN4 | c.1273A>T (p.Met425Leu) c.55A>T (p.Met19Leu) | |
15 | g.73332229T>C | CA393094458 | HCN4 | c.1273A>G (p.Met425Val) c.55A>G (p.Met19Val) | |
15 | g.73332229T>G | CA393094459 | HCN4 | c.1273A>C (p.Met425Leu) c.55A>C (p.Met19Leu) | |
15 | g.73332230C>A | CA393094460 | HCN4 | c.1272G>T (p.Met424Ile) c.54G>T (p.Met18Ile) | gnomAD v4 |
15 | g.73332230C>G | CA393094461 | HCN4 | c.1272G>C (p.Met424Ile) c.54G>C (p.Met18Ile) | |
15 | g.73332230C>T | CA393094462 | HCN4 | c.1272G>A (p.Met424Ile) c.54G>A (p.Met18Ile) | gnomAD v4 |
15 | g.73332231A>C | CA393094463 | HCN4 | c.1271T>G (p.Met424Arg) c.53T>G (p.Met18Arg) | |
15 | g.73332231A>G | CA393094464 | HCN4 | c.1271T>C (p.Met424Thr) c.53T>C (p.Met18Thr) | |
15 | g.73332231A>T | CA393094465 | HCN4 | c.1271T>A (p.Met424Lys) c.53T>A (p.Met18Lys) | |
15 | g.73332232T>A | CA393094466 | HCN4 | c.1270A>T (p.Met424Leu) c.52A>T (p.Met18Leu) | |
15 | g.73332232T>C | CA393094467 | HCN4 | c.1270A>G (p.Met424Val) c.52A>G (p.Met18Val) | |
15 | g.73332232T>G | CA393094468 | HCN4 | c.1270A>C (p.Met424Leu) c.52A>C (p.Met18Leu) | |
15 | g.73332233G>A | CA491152597 | HCN4 | c.1269C>T (p.Gly423=) c.51C>T (p.Gly17=) | |
15 | g.73332233G>C | CA491152598 | HCN4 | c.1269C>G (p.Gly423=) c.51C>G (p.Gly17=) | |
15 | g.73332233G>T | CA491152599 | HCN4 | c.1269C>A (p.Gly423=) c.51C>A (p.Gly17=) | |
15 | g.73332234C>A | CA393094471 | HCN4 | c.1268G>T (p.Gly423Val) c.50G>T (p.Gly17Val) | |
15 | g.73332234C>G | CA393094470 | HCN4 | c.1268G>C (p.Gly423Ala) c.50G>C (p.Gly17Ala) | |
15 | g.73332234C>T | CA393094469 | HCN4 | c.1268G>A (p.Gly423Asp) c.50G>A (p.Gly17Asp) | |
15 | g.73332235C>A | CA393094472 | HCN4 | c.1267G>T (p.Gly423Cys) c.49G>T (p.Gly17Cys) | |
15 | g.73332235C= | CA2187169826 | HCN4 | c.1267G= (p.Gly423=) c.49G= (p.Gly17=) | |
15 | g.73332235C>G | CA393094473 | HCN4 | c.1267G>C (p.Gly423Arg) c.49G>C (p.Gly17Arg) | |
15 | g.73332235C>T | CA7649333 | HCN4 | c.1267G>A (p.Gly423Ser) c.49G>A (p.Gly17Ser) | dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73332236G>A | CA7649334 | HCN4 | c.1266C>T (p.Ile422=) c.48C>T (p.Ile16=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
15 | g.73332236G>C | CA393094474 | HCN4 | c.1266C>G (p.Ile422Met) c.48C>G (p.Ile16Met) | |
15 | g.73332236G= | CA2187169828 | HCN4 | c.1266C= (p.Ile422=) c.48C= (p.Ile16=) | |
15 | g.73332236G>T | CA491152603 | HCN4 | c.1266C>A (p.Ile422=) c.48C>A (p.Ile16=) | |
15 | g.73332237A>C | CA393094475 | HCN4 | c.1265T>G (p.Ile422Ser) c.47T>G (p.Ile16Ser) | |
15 | g.73332237A>G | CA393094477 | HCN4 | c.1265T>C (p.Ile422Thr) c.47T>C (p.Ile16Thr) | |
15 | g.73332237A>T | CA393094476 | HCN4 | c.1265T>A (p.Ile422Asn) c.47T>A (p.Ile16Asn) | |
15 | g.73332238T>A | CA393094478 | HCN4 | c.1264A>T (p.Ile422Phe) c.46A>T (p.Ile16Phe) | |
15 | g.73332238T>C | CA393094479 | HCN4 | c.1264A>G (p.Ile422Val) c.46A>G (p.Ile16Val) | |
15 | g.73332238T>G | CA393094480 | HCN4 | c.1264A>C (p.Ile422Leu) c.46A>C (p.Ile16Leu) | |
15 | g.73332239G>A | CA491152605 | HCN4 | c.1263C>T (p.Leu421=) c.45C>T (p.Leu15=) | |
15 | g.73332239G>C | CA491152607 | HCN4 | c.1263C>G (p.Leu421=) c.45C>G (p.Leu15=) | |
15 | g.73332239G>T | CA491152606 | HCN4 | c.1263C>A (p.Leu421=) c.45C>A (p.Leu15=) | |
15 | g.73332240A>C | CA393094481 | HCN4 | c.1262T>G (p.Leu421Arg) c.44T>G (p.Leu15Arg) | |
15 | g.73332240A>G | CA393094482 | HCN4 | c.1262T>C (p.Leu421Pro) c.44T>C (p.Leu15Pro) | |
15 | g.73332240A>T | CA393094483 | HCN4 | c.1262T>A (p.Leu421His) c.44T>A (p.Leu15His) | |
15 | g.73332241G>A | CA393094484 | HCN4 | c.1261C>T (p.Leu421Phe) c.43C>T (p.Leu15Phe) | |
15 | g.73332241G>C | CA393094485 | HCN4 | c.1261C>G (p.Leu421Val) c.43C>G (p.Leu15Val) | |
15 | g.73332241G>T | CA393094486 | HCN4 | c.1261C>A (p.Leu421Ile) c.43C>A (p.Leu15Ile) | |
15 | g.73332242G>A | CA491152611 | HCN4 | c.1260C>T (p.Asn420=) c.42C>T (p.Asn14=) | gnomAD v4 |
15 | g.73332242G>C | CA393094487 | HCN4 | c.1260C>G (p.Asn420Lys) c.42C>G (p.Asn14Lys) | |
15 | g.73332242G>T | CA393094488 | HCN4 | c.1260C>A (p.Asn420Lys) c.42C>A (p.Asn14Lys) | |
15 | g.73332243T>A | CA393094491 | HCN4 | c.1259A>T (p.Asn420Ile) c.41A>T (p.Asn14Ile) | |
15 | g.73332243T>C | CA393094489 | HCN4 | c.1259A>G (p.Asn420Ser) c.41A>G (p.Asn14Ser) | |
15 | g.73332243T>G | CA393094490 | HCN4 | c.1259A>C (p.Asn420Thr) c.41A>C (p.Asn14Thr) | dbSNP |
15 | g.73332243T= | CA2187169831 | HCN4 | c.1259A= (p.Asn420=) c.41A= (p.Asn14=) | |
15 | g.73332244T>A | CA393094492 | HCN4 | c.1258A>T (p.Asn420Tyr) c.40A>T (p.Asn14Tyr) | |
15 | g.73332244T>C | CA393094493 | HCN4 | c.1258A>G (p.Asn420Asp) c.40A>G (p.Asn14Asp) | |
15 | g.73332244T>G | CA393094494 | HCN4 | c.1258A>C (p.Asn420His) c.40A>C (p.Asn14His) | |
15 | g.73332245C>A | CA7649335 | HCN4 | c.1257G>T (p.Val419=) c.39G>T (p.Val13=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73332245C= | CA2187169834 | HCN4 | c.1257G= (p.Val419=) c.39G= (p.Val13=) | |
15 | g.73332245C>G | CA491152616 | HCN4 | c.1257G>C (p.Val419=) c.39G>C (p.Val13=) | gnomAD v4 |
15 | g.73332245C>T | CA491152617 | HCN4 | c.1257G>A (p.Val419=) c.39G>A (p.Val13=) | COSMIC |
15 | g.73332246A>C | CA393094495 | HCN4 | c.1256T>G (p.Val419Gly) c.38T>G (p.Val13Gly) | ClinVar |
15 | g.73332246A>G | CA393094496 | HCN4 | c.1256T>C (p.Val419Ala) c.38T>C (p.Val13Ala) | gnomAD v4 |
15 | g.73332246A>T | CA393094497 | HCN4 | c.1256T>A (p.Val419Glu) c.38T>A (p.Val13Glu) | |
15 | g.73332247C>A | CA393094498 | HCN4 | c.1255G>T (p.Val419Leu) c.37G>T (p.Val13Leu) | |
15 | g.73332247C= | CA2187169837 | HCN4 | c.1255G= (p.Val419=) c.37G= (p.Val13=) | |
15 | g.73332247C>G | CA393094499 | HCN4 | c.1255G>C (p.Val419Leu) c.37G>C (p.Val13Leu) | |
15 | g.73332247C>T | CA393094500 | HCN4 | c.1255G>A (p.Val419Met) c.37G>A (p.Val13Met) | ClinVar dbSNP gnomAD v4 COSMIC |
15 | g.73332248G>A | CA7649336 | HCN4 | c.1254C>T (p.Ile418=) c.36C>T (p.Ile12=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73332248G>C | CA393094501 | HCN4 | c.1254C>G (p.Ile418Met) c.36C>G (p.Ile12Met) | |
15 | g.73332248G= | CA2187169842 | HCN4 | c.1254C= (p.Ile418=) c.36C= (p.Ile12=) | |
15 | g.73332248G>T | CA491152619 | HCN4 | c.1254C>A (p.Ile418=) c.36C>A (p.Ile12=) | COSMIC |
15 | g.73332249A>C | CA393094502 | HCN4 | c.1253T>G (p.Ile418Ser) c.35T>G (p.Ile12Ser) | |
15 | g.73332249A>G | CA393094503 | HCN4 | c.1253T>C (p.Ile418Thr) c.35T>C (p.Ile12Thr) | |
15 | g.73332249A>T | CA393094504 | HCN4 | c.1253T>A (p.Ile418Asn) c.35T>A (p.Ile12Asn) | |
15 | g.73332250T>A | CA393094505 | HCN4 | c.1252A>T (p.Ile418Phe) c.34A>T (p.Ile12Phe) | gnomAD v4 |
15 | g.73332250T>C | CA393094506 | HCN4 | c.1252A>G (p.Ile418Val) c.34A>G (p.Ile12Val) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73332250T>G | CA393094507 | HCN4 | c.1252A>C (p.Ile418Leu) c.34A>C (p.Ile12Leu) | |
15 | g.73332250T= | CA2187169847 | HCN4 | c.1252A= (p.Ile418=) c.34A= (p.Ile12=) | |
15 | g.73332251G>A | CA491152620 | HCN4 | c.1251C>T (p.Arg417=) c.33C>T (p.Arg11=) | gnomAD v4 |
15 | g.73332251G>C | CA491152623 | HCN4 | c.1251C>G (p.Arg417=) c.33C>G (p.Arg11=) | |
15 | g.73332251G>T | CA491152621 | HCN4 | c.1251C>A (p.Arg417=) c.33C>A (p.Arg11=) | |
15 | g.73332252C>A | CA393094508 | HCN4 | c.1250G>T (p.Arg417Leu) c.32G>T (p.Arg11Leu) | |
15 | g.73332252C= | CA2187169849 | HCN4 | c.1250G= (p.Arg417=) c.32G= (p.Arg11=) | |
15 | g.73332252C>G | CA393094509 | HCN4 | c.1250G>C (p.Arg417Pro) c.32G>C (p.Arg11Pro) | |
15 | g.73332252C>T | CA272673953 | HCN4 | c.1250G>A (p.Arg417His) c.32G>A (p.Arg11His) | ClinVar dbSNP gnomAD v4 COSMIC |
15 | g.73332253G>A | CA393094510 | HCN4 | c.1249C>T (p.Arg417Cys) c.31C>T (p.Arg11Cys) | |
15 | g.73332253G>C | CA7649337 | HCN4 | c.1249C>G (p.Arg417Gly) c.31C>G (p.Arg11Gly) | dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73332253G= | CA2187169854 | HCN4 | c.1249C= (p.Arg417=) c.31C= (p.Arg11=) | |
15 | g.73332253G>T | CA393094511 | HCN4 | c.1249C>A (p.Arg417Ser) c.31C>A (p.Arg11Ser) | |
15 | g.73332254C>A | CA491152625 | HCN4 | c.1248G>T (p.Val416=) c.30G>T (p.Val10=) | |
15 | g.73332254C>G | CA491152627 | HCN4 | c.1248G>C (p.Val416=) c.30G>C (p.Val10=) | |
15 | g.73332254C>T | CA491152628 | HCN4 | c.1248G>A (p.Val416=) c.30G>A (p.Val10=) | ClinVar |
15 | g.73332255A>C | CA393094514 | HCN4 | c.1247T>G (p.Val416Gly) c.29T>G (p.Val10Gly) | |
15 | g.73332255A>G | CA393094513 | HCN4 | c.1247T>C (p.Val416Ala) c.29T>C (p.Val10Ala) | |
15 | g.73332255A>T | CA393094512 | HCN4 | c.1247T>A (p.Val416Glu) c.29T>A (p.Val10Glu) | dbSNP |
15 | g.73332256C>A | CA393094515 | HCN4 | c.1246G>T (p.Val416Leu) c.28G>T (p.Val10Leu) | ClinVar dbSNP |
15 | g.73332256C= | CA2187169857 | HCN4 | c.1246G= (p.Val416=) c.28G= (p.Val10=) | |
15 | g.73332256C>G | CA393094516 | HCN4 | c.1246G>C (p.Val416Leu) c.28G>C (p.Val10Leu) | dbSNP |
15 | g.73332256C>T | CA393094517 | HCN4 | c.1246G>A (p.Val416Met) c.28G>A (p.Val10Met) | gnomAD v4 |
15 | g.73332257C>A | CA491152630 | HCN4 | c.1245G>T (p.Val415=) c.27G>T (p.Val9=) | |
15 | g.73332257C>G | CA491152631 | HCN4 | c.1245G>C (p.Val415=) c.27G>C (p.Val9=) | |
15 | g.73332257C>T | CA491152633 | HCN4 | c.1245G>A (p.Val415=) c.27G>A (p.Val9=) | |
15 | g.73332258A>C | CA393094518 | HCN4 | c.1244T>G (p.Val415Gly) c.26T>G (p.Val9Gly) | |
15 | g.73332258A>G | CA393094519 | HCN4 | c.1244T>C (p.Val415Ala) c.26T>C (p.Val9Ala) | |
15 | g.73332258A>T | CA393094520 | HCN4 | c.1244T>A (p.Val415Glu) c.26T>A (p.Val9Glu) | |
15 | g.73332259C>A | CA393094521 | HCN4 | c.1243G>T (p.Val415Leu) c.25G>T (p.Val9Leu) | |
15 | g.73332259C= | CA2187169866 | HCN4 | c.1243G= (p.Val415=) c.25G= (p.Val9=) | |
15 | g.73332259C>G | CA393094522 | HCN4 | c.1243G>C (p.Val415Leu) c.25G>C (p.Val9Leu) | |
15 | g.73332259C>T | CA7649338 | HCN4 | c.1243G>A (p.Val415Met) c.25G>A (p.Val9Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73332260G>A | CA7649339 | HCN4 | c.1242C>T (p.Ala414=) c.24C>T (p.Ala8=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73332260G>C | CA491152637 | HCN4 | c.1242C>G (p.Ala414=) c.24C>G (p.Ala8=) | |
15 | g.73332260G= | CA2187169870 | HCN4 | c.1242C= (p.Ala414=) c.24C= (p.Ala8=) | |
15 | g.73332260G>T | CA491152636 | HCN4 | c.1242C>A (p.Ala414=) c.24C>A (p.Ala8=) | |
15 | g.73332261G>A | CA393094523 | HCN4 | c.1241C>T (p.Ala414Val) c.23C>T (p.Ala8Val) | |
15 | g.73332261G>C | CA16043944 | HCN4 | c.1241C>G (p.Ala414Gly) c.23C>G (p.Ala8Gly) | ClinVar dbSNP |
15 | g.73332261G= | CA2187169874 | HCN4 | c.1241C= (p.Ala414=) c.23C= (p.Ala8=) | |
15 | g.73332261G>T | CA393094524 | HCN4 | c.1241C>A (p.Ala414Asp) c.23C>A (p.Ala8Asp) | |
15 | g.73332262C>A | CA393094525 | HCN4 | c.1240G>T (p.Ala414Ser) c.22G>T (p.Ala8Ser) | |
15 | g.73332262C= | CA2187169879 | HCN4 | c.1240G= (p.Ala414=) c.22G= (p.Ala8=) | |
15 | g.73332262C>G | CA393094526 | HCN4 | c.1240G>C (p.Ala414Pro) c.22G>C (p.Ala8Pro) | |
15 | g.73332262C>T | CA7649340 | HCN4 | c.1240G>A (p.Ala414Thr) c.22G>A (p.Ala8Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73332263G>A | CA7649341 | HCN4 | c.1239C>T (p.Ser413=) c.21C>T (p.Ser7=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73332263G>C | CA393094527 | HCN4 | c.1239C>G (p.Ser413Arg) c.21C>G (p.Ser7Arg) | |
15 | g.73332263G= | CA2187169882 | HCN4 | c.1239C= (p.Ser413=) c.21C= (p.Ser7=) | |
15 | g.73332263G>T | CA393094528 | HCN4 | c.1239C>A (p.Ser413Arg) c.21C>A (p.Ser7Arg) | |
15 | g.73332264C>A | CA393094529 | HCN4 | c.1238G>T (p.Ser413Ile) c.20G>T (p.Ser7Ile) | |
15 | g.73332264C>G | CA393094530 | HCN4 | c.1238G>C (p.Ser413Thr) c.20G>C (p.Ser7Thr) | |
15 | g.73332264C>T | CA393094531 | HCN4 | c.1238G>A (p.Ser413Asn) c.20G>A (p.Ser7Asn) | |
15 | g.73332265T>A | CA393094534 | HCN4 | c.1237A>T (p.Ser413Cys) c.19A>T (p.Ser7Cys) | |
15 | g.73332265T>C | CA393094533 | HCN4 | c.1237A>G (p.Ser413Gly) c.19A>G (p.Ser7Gly) | ClinVar dbSNP |
15 | g.73332265T>G | CA393094532 | HCN4 | c.1237A>C (p.Ser413Arg) c.19A>C (p.Ser7Arg) | |
15 | g.73332265T= | CA2187169885 | HCN4 | c.1237A= (p.Ser413=) c.19A= (p.Ser7=) | |
15 | g.73332266G>A | CA491152643 | HCN4 | c.1236C>T (p.Ala412=) c.18C>T (p.Ala6=) | |
15 | g.73332266G>C | CA491152644 | HCN4 | c.1236C>G (p.Ala412=) c.18C>G (p.Ala6=) | |
15 | g.73332266G>T | CA491152645 | HCN4 | c.1236C>A (p.Ala412=) c.18C>A (p.Ala6=) | |
15 | g.73332267G>A | CA393094535 | HCN4 | c.1235C>T (p.Ala412Val) c.17C>T (p.Ala6Val) | |
15 | g.73332267G>C | CA393094536 | HCN4 | c.1235C>G (p.Ala412Gly) c.17C>G (p.Ala6Gly) | COSMIC |
15 | g.73332267G>T | CA393094537 | HCN4 | c.1235C>A (p.Ala412Asp) c.17C>A (p.Ala6Asp) | |
15 | g.73332268C>A | CA393094538 | HCN4 | c.1234G>T (p.Ala412Ser) c.16G>T (p.Ala6Ser) | |
15 | g.73332268C>G | CA393094539 | HCN4 | c.1234G>C (p.Ala412Pro) c.16G>C (p.Ala6Pro) | |
15 | g.73332268C>T | CA393094540 | HCN4 | c.1234G>A (p.Ala412Thr) c.16G>A (p.Ala6Thr) | |
15 | g.73332269C>A | CA491152649 | HCN4 | c.1233G>T (p.Leu411=) c.15G>T (p.Leu5=) | |
15 | g.73332269C>G | CA491152650 | HCN4 | c.1233G>C (p.Leu411=) c.15G>C (p.Leu5=) | gnomAD v4 |
15 | g.73332269C>T | CA491152651 | HCN4 | c.1233G>A (p.Leu411=) c.15G>A (p.Leu5=) | gnomAD v4 |
15 | g.73332270A>C | CA393094541 | HCN4 | c.1232T>G (p.Leu411Arg) c.14T>G (p.Leu5Arg) | |
15 | g.73332270A>G | CA393094543 | HCN4 | c.1232T>C (p.Leu411Pro) c.14T>C (p.Leu5Pro) | |
15 | g.73332270A>T | CA393094542 | HCN4 | c.1232T>A (p.Leu411Gln) c.14T>A (p.Leu5Gln) | |
15 | g.73332271G>A | CA491152655 | HCN4 | c.1231C>T (p.Leu411=) c.13C>T (p.Leu5=) | |
15 | g.73332271G>C | CA393094544 | HCN4 | c.1231C>G (p.Leu411Val) c.13C>G (p.Leu5Val) | ClinVar gnomAD v4 |
15 | g.73332271G= | CA2187169888 | HCN4 | c.1231C= (p.Leu411=) c.13C= (p.Leu5=) | |
15 | g.73332271G>T | CA393094545 | HCN4 | c.1231C>A (p.Leu411Met) c.13C>A (p.Leu5Met) | dbSNP gnomAD v2 |
15 | g.73332272G>A | CA491152656 | HCN4 | c.1230C>T (p.Asp410=) c.12C>T (p.Asp4=) | |
15 | g.73332272G>C | CA393094546 | HCN4 | c.1230C>G (p.Asp410Glu) c.12C>G (p.Asp4Glu) | |
15 | g.73332272G>T | CA393094547 | HCN4 | c.1230C>A (p.Asp410Glu) c.12C>A (p.Asp4Glu) | |
15 | g.73332273T>A | CA393094548 | HCN4 | c.1229A>T (p.Asp410Val) c.11A>T (p.Asp4Val) | |
15 | g.73332273T>C | CA393094549 | HCN4 | c.1229A>G (p.Asp410Gly) c.11A>G (p.Asp4Gly) | |
15 | g.73332273T>G | CA393094550 | HCN4 | c.1229A>C (p.Asp410Ala) c.11A>C (p.Asp4Ala) | |
15 | g.73332274C>A | CA393094551 | HCN4 | c.1228G>T (p.Asp410Tyr) c.10G>T (p.Asp4Tyr) | gnomAD v4 COSMIC |
15 | g.73332274C>G | CA393094552 | HCN4 | c.1228G>C (p.Asp410His) c.10G>C (p.Asp4His) | |
15 | g.73332274C>T | CA393094553 | HCN4 | c.1228G>A (p.Asp410Asn) c.10G>A (p.Asp4Asn) | COSMIC |
15 | g.73332275G>A | CA7649342 | HCN4 | c.1227C>T (p.Tyr409=) c.9C>T (p.Tyr3=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73332275G>C | CA393094555 | HCN4 | c.1227C>G (p.Tyr409Ter) c.9C>G (p.Tyr3Ter) | |
15 | g.73332275G= | CA2187169893 | HCN4 | c.1227C= (p.Tyr409=) c.9C= (p.Tyr3=) | |
15 | g.73332275G>T | CA393094554 | HCN4 | c.1227C>A (p.Tyr409Ter) c.9C>A (p.Tyr3Ter) | |
15 | g.73332276T>A | CA393094556 | HCN4 | c.1226A>T (p.Tyr409Phe) c.8A>T (p.Tyr3Phe) | |
15 | g.73332276T>C | CA393094557 | HCN4 | c.1226A>G (p.Tyr409Cys) c.8A>G (p.Tyr3Cys) | |
15 | g.73332276T>G | CA393094558 | HCN4 | c.1226A>C (p.Tyr409Ser) c.8A>C (p.Tyr3Ser) | |
15 | g.73332277A>C | CA393094559 | HCN4 | c.1225T>G (p.Tyr409Asp) c.7T>G (p.Tyr3Asp) | |
15 | g.73332277A>G | CA393094560 | HCN4 | c.1225T>C (p.Tyr409His) c.7T>C (p.Tyr3His) | |
15 | g.73332277A>T | CA393094561 | HCN4 | c.1225T>A (p.Tyr409Asn) c.7T>A (p.Tyr3Asn) | |
15 | g.73332278G>A | CA491152659 | HCN4 | c.1224C>T (p.Thr408=) c.6C>T (p.Thr2=) | |
15 | g.73332278G>C | CA491152660 | HCN4 | c.1224C>G (p.Thr408=) c.6C>G (p.Thr2=) | |
15 | g.73332278G>T | CA491152661 | HCN4 | c.1224C>A (p.Thr408=) c.6C>A (p.Thr2=) | |
15 | g.73332279G>A | CA393094562 | HCN4 | c.1223C>T (p.Thr408Ile) c.5C>T (p.Thr2Ile) | dbSNP gnomAD v2 COSMIC |
15 | g.73332279G>C | CA393094563 | HCN4 | c.1223C>G (p.Thr408Ser) c.5C>G (p.Thr2Ser) | |
15 | g.73332279G= | CA2187169900 | HCN4 | c.1223C= (p.Thr408=) c.5C= (p.Thr2=) | |
15 | g.73332279G>T | CA393094564 | HCN4 | c.1223C>A (p.Thr408Asn) c.5C>A (p.Thr2Asn) |