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.73323383T>A | CA393088327 | HCN4 | c.2710A>T (p.Ile904Leu) c.1492A>T (p.Ile498Leu) | |
| 15 | g.73323383T>C | CA393088329 | HCN4 | c.2710A>G (p.Ile904Val) c.1492A>G (p.Ile498Val) | dbSNP gnomAD v4 |
| 15 | g.73323383T>G | CA393088330 | HCN4 | c.2710A>C (p.Ile904Leu) c.1492A>C (p.Ile498Leu) | |
| 15 | g.73323383T= | CA2187188172 | HCN4 | c.2710A= (p.Ile904=) c.1492A= (p.Ile498=) | |
| 15 | g.73323389_73323391dup | CA919589489 | HCN4 | c.2708_2710dup (p.Thr903_Ile904insThr) c.1490_1492dup (p.Thr497_Ile498insThr) | dbSNP |
| 15 | g.73323384G>A | CA491478443 | HCN4 | c.2709C>T (p.Thr903=) c.1491C>T (p.Thr497=) | |
| 15 | g.73323384G>C | CA491478442 | HCN4 | c.2709C>G (p.Thr903=) c.1491C>G (p.Thr497=) | |
| 15 | g.73323384G>T | CA491478441 | HCN4 | c.2709C>A (p.Thr903=) c.1491C>A (p.Thr497=) | gnomAD v4 |
| 15 | g.73323385G>A | CA393088332 | HCN4 | c.2708C>T (p.Thr903Ile) c.1490C>T (p.Thr497Ile) | gnomAD v4 |
| 15 | g.73323385G>C | CA393088333 | HCN4 | c.2708C>G (p.Thr903Ser) c.1490C>G (p.Thr497Ser) | |
| 15 | g.73323385G>T | CA393088335 | HCN4 | c.2708C>A (p.Thr903Asn) c.1490C>A (p.Thr497Asn) | |
| 15 | g.73323386T>A | CA393088337 | HCN4 | c.2707A>T (p.Thr903Ser) c.1489A>T (p.Thr497Ser) | |
| 15 | g.73323386T>C | CA393088340 | HCN4 | c.2707A>G (p.Thr903Ala) c.1489A>G (p.Thr497Ala) | |
| 15 | g.73323386T>G | CA393088338 | HCN4 | c.2707A>C (p.Thr903Pro) c.1489A>C (p.Thr497Pro) | |
| 15 | g.73323387G>A | CA491478455 | HCN4 | c.2706C>T (p.Thr902=) c.1488C>T (p.Thr496=) | |
| 15 | g.73323387G>C | CA491478458 | HCN4 | c.2706C>G (p.Thr902=) c.1488C>G (p.Thr496=) | |
| 15 | g.73323387G>T | CA491478457 | HCN4 | c.2706C>A (p.Thr902=) c.1488C>A (p.Thr496=) | |
| 15 | g.73323388G>A | CA393088341 | HCN4 | c.2705C>T (p.Thr902Ile) c.1487C>T (p.Thr496Ile) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323388G>C | CA393088343 | HCN4 | c.2705C>G (p.Thr902Ser) c.1487C>G (p.Thr496Ser) | |
| 15 | g.73323388G= | CA2187188175 | HCN4 | c.2705C= (p.Thr902=) c.1487C= (p.Thr496=) | |
| 15 | g.73323388G>T | CA393088344 | HCN4 | c.2705C>A (p.Thr902Asn) c.1487C>A (p.Thr496Asn) | gnomAD v4 |
| 15 | g.73323389T>A | CA393088346 | HCN4 | c.2704A>T (p.Thr902Ser) c.1486A>T (p.Thr496Ser) | |
| 15 | g.73323389T>C | CA393088348 | HCN4 | c.2704A>G (p.Thr902Ala) c.1486A>G (p.Thr496Ala) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323389T>G | CA393088350 | HCN4 | c.2704A>C (p.Thr902Pro) c.1486A>C (p.Thr496Pro) | |
| 15 | g.73323389T= | CA2187188178 | HCN4 | c.2704A= (p.Thr902=) c.1486A= (p.Thr496=) | |
| 15 | g.73323390G>A | CA7648967 | HCN4 | c.2703C>T (p.Ala901=) c.1485C>T (p.Ala495=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323390G>C | CA491478467 | HCN4 | c.2703C>G (p.Ala901=) c.1485C>G (p.Ala495=) | |
| 15 | g.73323390G= | CA2187188180 | HCN4 | c.2703C= (p.Ala901=) c.1485C= (p.Ala495=) | |
| 15 | g.73323390G>T | CA491478468 | HCN4 | c.2703C>A (p.Ala901=) c.1485C>A (p.Ala495=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323391G>A | CA393088353 | HCN4 | c.2702C>T (p.Ala901Val) c.1484C>T (p.Ala495Val) | |
| 15 | g.73323391G>C | CA393088354 | HCN4 | c.2702C>G (p.Ala901Gly) c.1484C>G (p.Ala495Gly) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323391G= | CA2187188185 | HCN4 | c.2702C= (p.Ala901=) c.1484C= (p.Ala495=) | |
| 15 | g.73323391G>T | CA393088357 | HCN4 | c.2702C>A (p.Ala901Asp) c.1484C>A (p.Ala495Asp) | gnomAD v4 |
| 15 | g.73323392C>A | CA393088358 | HCN4 | c.2701G>T (p.Ala901Ser) c.1483G>T (p.Ala495Ser) | gnomAD v4 |
| 15 | g.73323392C= | CA2187188189 | HCN4 | c.2701G= (p.Ala901=) c.1483G= (p.Ala495=) | |
| 15 | g.73323392C>G | CA393088360 | HCN4 | c.2701G>C (p.Ala901Pro) c.1483G>C (p.Ala495Pro) | dbSNP |
| 15 | g.73323392C>T | CA7648968 | HCN4 | c.2701G>A (p.Ala901Thr) c.1483G>A (p.Ala495Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323393G>A | CA7648970 | HCN4 | c.2700C>T (p.Ala900=) c.1482C>T (p.Ala494=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323393G>C | CA491478477 | HCN4 | c.2700C>G (p.Ala900=) c.1482C>G (p.Ala494=) | |
| 15 | g.73323393G= | CA2187188197 | HCN4 | c.2700C= (p.Ala900=) c.1482C= (p.Ala494=) | |
| 15 | g.73323393G>T | CA7648969 | HCN4 | c.2700C>A (p.Ala900=) c.1482C>A (p.Ala494=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323394G>A | CA393088365 | HCN4 | c.2699C>T (p.Ala900Val) c.1481C>T (p.Ala494Val) | gnomAD v4 |
| 15 | g.73323394G>C | CA393088367 | HCN4 | c.2699C>G (p.Ala900Gly) c.1481C>G (p.Ala494Gly) | |
| 15 | g.73323394G>T | CA393088369 | HCN4 | c.2699C>A (p.Ala900Asp) c.1481C>A (p.Ala494Asp) | gnomAD v4 |
| 15 | g.73323395C>A | CA393088370 | HCN4 | c.2698G>T (p.Ala900Ser) c.1480G>T (p.Ala494Ser) | |
| 15 | g.73323395C= | CA2187188202 | HCN4 | c.2698G= (p.Ala900=) c.1480G= (p.Ala494=) | |
| 15 | g.73323395C>G | CA393088372 | HCN4 | c.2698G>C (p.Ala900Pro) c.1480G>C (p.Ala494Pro) | dbSNP |
| 15 | g.73323395C>T | CA393088374 | HCN4 | c.2698G>A (p.Ala900Thr) c.1480G>A (p.Ala494Thr) | dbSNP gnomAD v4 |
| 15 | g.73323396T>A | CA491478482 | HCN4 | c.2697A>T (p.Val899=) c.1479A>T (p.Val493=) | |
| 15 | g.73323396T>C | CA491478484 | HCN4 | c.2697A>G (p.Val899=) c.1479A>G (p.Val493=) | |
| 15 | g.73323396T>G | CA491478486 | HCN4 | c.2697A>C (p.Val899=) c.1479A>C (p.Val493=) | dbSNP |
| 15 | g.73323396T= | CA2187188205 | HCN4 | c.2697A= (p.Val899=) c.1479A= (p.Val493=) | |
| 15 | g.73323397A>C | CA393088376 | HCN4 | c.2696T>G (p.Val899Gly) c.1478T>G (p.Val493Gly) | ClinVar |
| 15 | g.73323397A>G | CA393088378 | HCN4 | c.2696T>C (p.Val899Ala) c.1478T>C (p.Val493Ala) | dbSNP |
| 15 | g.73323397A>T | CA393088380 | HCN4 | c.2696T>A (p.Val899Glu) c.1478T>A (p.Val493Glu) | |
| 15 | g.73323398C>A | CA393088381 | HCN4 | c.2695G>T (p.Val899Leu) c.1477G>T (p.Val493Leu) | gnomAD v4 |
| 15 | g.73323398C= | CA2187188210 | HCN4 | c.2695G= (p.Val899=) c.1477G= (p.Val493=) | |
| 15 | g.73323398C>G | CA393088383 | HCN4 | c.2695G>C (p.Val899Leu) c.1477G>C (p.Val493Leu) | |
| 15 | g.73323398C>T | CA272664364 | HCN4 | c.2695G>A (p.Val899Ile) c.1477G>A (p.Val493Ile) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323399G>A | CA7648971 | HCN4 | c.2694C>T (p.Gly898=) c.1476C>T (p.Gly492=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323399G>C | CA491478494 | HCN4 | c.2694C>G (p.Gly898=) c.1476C>G (p.Gly492=) | |
| 15 | g.73323399G= | CA2187188217 | HCN4 | c.2694C= (p.Gly898=) c.1476C= (p.Gly492=) | |
| 15 | g.73323399G>T | CA491478495 | HCN4 | c.2694C>A (p.Gly898=) c.1476C>A (p.Gly492=) | ClinVar dbSNP |
| 15 | g.73323400C>A | CA393088387 | HCN4 | c.2693G>T (p.Gly898Val) c.1475G>T (p.Gly492Val) | |
| 15 | g.73323400C>G | CA393088391 | HCN4 | c.2693G>C (p.Gly898Ala) c.1475G>C (p.Gly492Ala) | |
| 15 | g.73323400C>T | CA393088389 | HCN4 | c.2693G>A (p.Gly898Asp) c.1475G>A (p.Gly492Asp) | |
| 15 | g.73323401C>A | CA393088392 | HCN4 | c.2692G>T (p.Gly898Cys) c.1474G>T (p.Gly492Cys) | |
| 15 | g.73323401C>G | CA393088395 | HCN4 | c.2692G>C (p.Gly898Arg) c.1474G>C (p.Gly492Arg) | |
| 15 | g.73323401C>T | CA393088393 | HCN4 | c.2692G>A (p.Gly898Ser) c.1474G>A (p.Gly492Ser) | |
| 15 | g.73323402A>C | CA491478501 | HCN4 | c.2691T>G (p.Ala897=) c.1473T>G (p.Ala491=) | ClinVar gnomAD v4 |
| 15 | g.73323402A>G | CA491478499 | HCN4 | c.2691T>C (p.Ala897=) c.1473T>C (p.Ala491=) | gnomAD v4 |
| 15 | g.73323402A>T | CA491478500 | HCN4 | c.2691T>A (p.Ala897=) c.1473T>A (p.Ala491=) | |
| 15 | g.73323403G>A | CA393088396 | HCN4 | c.2690C>T (p.Ala897Val) c.1472C>T (p.Ala491Val) | |
| 15 | g.73323403G>C | CA393088397 | HCN4 | c.2690C>G (p.Ala897Gly) c.1472C>G (p.Ala491Gly) | |
| 15 | g.73323403G>T | CA393088399 | HCN4 | c.2690C>A (p.Ala897Asp) c.1472C>A (p.Ala491Asp) | |
| 15 | g.73323404C>A | CA393088400 | HCN4 | c.2689G>T (p.Ala897Ser) c.1471G>T (p.Ala491Ser) | |
| 15 | g.73323404C= | CA2187188220 | HCN4 | c.2689G= (p.Ala897=) c.1471G= (p.Ala491=) | |
| 15 | g.73323404C>G | CA393088402 | HCN4 | c.2689G>C (p.Ala897Pro) c.1471G>C (p.Ala491Pro) | |
| 15 | g.73323404C>T | CA393088403 | HCN4 | c.2689G>A (p.Ala897Thr) c.1471G>A (p.Ala491Thr) | |
| 15 | g.73323405T>A | CA491478511 | HCN4 | c.2688A>T (p.Ser896=) c.1470A>T (p.Ser490=) | |
| 15 | g.73323405T>C | CA491478510 | HCN4 | c.2688A>G (p.Ser896=) c.1470A>G (p.Ser490=) | |
| 15 | g.73323405T>G | CA491478509 | HCN4 | c.2688A>C (p.Ser896=) c.1470A>C (p.Ser490=) | gnomAD v3 gnomAD v4 |
| 15 | g.73323407_73323409dup | CA971394813 | HCN4 | c.2686_2688dup (p.Ser896_Ala897insSer) c.1468_1470dup (p.Ser490_Ala491insSer) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73323406G>A | CA393088405 | HCN4 | c.2687C>T (p.Ser896Leu) c.1469C>T (p.Ser490Leu) | gnomAD v4 |
| 15 | g.73323406G>C | CA393088407 | HCN4 | c.2687C>G (p.Ser896Ter) c.1469C>G (p.Ser490Ter) | |
| 15 | g.73323406G>T | CA393088408 | HCN4 | c.2687C>A (p.Ser896Ter) c.1469C>A (p.Ser490Ter) | |
| 15 | g.73323407A>C | CA393088410 | HCN4 | c.2686T>G (p.Ser896Ala) c.1468T>G (p.Ser490Ala) | |
| 15 | g.73323407A>G | CA393088412 | HCN4 | c.2686T>C (p.Ser896Pro) c.1468T>C (p.Ser490Pro) | |
| 15 | g.73323407A>T | CA393088413 | HCN4 | c.2686T>A (p.Ser896Thr) c.1468T>A (p.Ser490Thr) | |
| 15 | g.73323408T>A | CA491478521 | HCN4 | c.2685A>T (p.Pro895=) c.1467A>T (p.Pro489=) | |
| 15 | g.73323408T>C | CA491478519 | HCN4 | c.2685A>G (p.Pro895=) c.1467A>G (p.Pro489=) | COSMIC |
| 15 | g.73323408T>G | CA491478520 | HCN4 | c.2685A>C (p.Pro895=) c.1467A>C (p.Pro489=) | |
| 15 | g.73323409G>A | CA393088415 | HCN4 | c.2684C>T (p.Pro895Leu) c.1466C>T (p.Pro489Leu) | |
| 15 | g.73323409G>C | CA393088418 | HCN4 | c.2684C>G (p.Pro895Arg) c.1466C>G (p.Pro489Arg) | gnomAD v4 |
| 15 | g.73323409G>T | CA393088416 | HCN4 | c.2684C>A (p.Pro895Gln) c.1466C>A (p.Pro489Gln) | |
| 15 | g.73323410G>A | CA393088420 | HCN4 | c.2683C>T (p.Pro895Ser) c.1465C>T (p.Pro489Ser) | |
| 15 | g.73323410G>C | CA393088422 | HCN4 | c.2683C>G (p.Pro895Ala) c.1465C>G (p.Pro489Ala) | |
| 15 | g.73323410G= | CA2187188224 | HCN4 | c.2683C= (p.Pro895=) c.1465C= (p.Pro489=) | |
| 15 | g.73323410G>T | CA393088423 | HCN4 | c.2683C>A (p.Pro895Thr) c.1465C>A (p.Pro489Thr) | gnomAD v4 |
| 15 | g.73323410_73323411insA | CA393088424 | HCN4 | c.2682_2683insT (p.Pro895SerfsTer?) c.1464_1465insT (p.Pro489SerfsTer?) | dbSNP |
| 15 | g.73323411T>A | CA491478531 | HCN4 | c.2682A>T (p.Thr894=) c.1464A>T (p.Thr488=) | |
| 15 | g.73323411T>C | CA491478533 | HCN4 | c.2682A>G (p.Thr894=) c.1464A>G (p.Thr488=) | ClinVar gnomAD v4 |
| 15 | g.73323411T>G | CA491478534 | HCN4 | c.2682A>C (p.Thr894=) c.1464A>C (p.Thr488=) | gnomAD v4 |
| 15 | g.73323412G>A | CA393088425 | HCN4 | c.2681C>T (p.Thr894Ile) c.1463C>T (p.Thr488Ile) | gnomAD v4 |
| 15 | g.73323412G>C | CA393088426 | HCN4 | c.2681C>G (p.Thr894Arg) c.1463C>G (p.Thr488Arg) | |
| 15 | g.73323412G= | CA2187188229 | HCN4 | c.2681C= (p.Thr894=) c.1463C= (p.Thr488=) | |
| 15 | g.73323412G>T | CA393088427 | HCN4 | c.2681C>A (p.Thr894Lys) c.1463C>A (p.Thr488Lys) | dbSNP gnomAD v2 |
| 15 | g.73323413T>A | CA393088428 | HCN4 | c.2680A>T (p.Thr894Ser) c.1462A>T (p.Thr488Ser) | |
| 15 | g.73323413T>C | CA393088429 | HCN4 | c.2680A>G (p.Thr894Ala) c.1462A>G (p.Thr488Ala) | |
| 15 | g.73323413T>G | CA393088430 | HCN4 | c.2680A>C (p.Thr894Pro) c.1462A>C (p.Thr488Pro) | |
| 15 | g.73323414G>A | CA491478541 | HCN4 | c.2679C>T (p.Pro893=) c.1461C>T (p.Pro487=) | |
| 15 | g.73323414G>C | CA491478542 | HCN4 | c.2679C>G (p.Pro893=) c.1461C>G (p.Pro487=) | |
| 15 | g.73323414G>T | CA491478543 | HCN4 | c.2679C>A (p.Pro893=) c.1461C>A (p.Pro487=) | |
| 15 | g.73323415G>A | CA393088432 | HCN4 | c.2678C>T (p.Pro893Leu) c.1460C>T (p.Pro487Leu) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73323415G>C | CA393088433 | HCN4 | c.2678C>G (p.Pro893Arg) c.1460C>G (p.Pro487Arg) | |
| 15 | g.73323415G= | CA2187188233 | HCN4 | c.2678C= (p.Pro893=) c.1460C= (p.Pro487=) | |
| 15 | g.73323415G>T | CA393088431 | HCN4 | c.2678C>A (p.Pro893His) c.1460C>A (p.Pro487His) | gnomAD v4 |
| 15 | g.73323416G>A | CA393088434 | HCN4 | c.2677C>T (p.Pro893Ser) c.1459C>T (p.Pro487Ser) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323416G>C | CA393088435 | HCN4 | c.2677C>G (p.Pro893Ala) c.1459C>G (p.Pro487Ala) | ClinVar |
| 15 | g.73323416G= | CA2187188237 | HCN4 | c.2677C= (p.Pro893=) c.1459C= (p.Pro487=) | |
| 15 | g.73323416G>T | CA393088436 | HCN4 | c.2677C>A (p.Pro893Thr) c.1459C>A (p.Pro487Thr) | |
| 15 | g.73323417A>C | CA491478547 | HCN4 | c.2676T>G (p.Ala892=) c.1458T>G (p.Ala486=) | |
| 15 | g.73323417A>G | CA491478548 | HCN4 | c.2676T>C (p.Ala892=) c.1458T>C (p.Ala486=) | |
| 15 | g.73323417A>T | CA491478549 | HCN4 | c.2676T>A (p.Ala892=) c.1458T>A (p.Ala486=) | |
| 15 | g.73323418G>A | CA393088437 | HCN4 | c.2675C>T (p.Ala892Val) c.1457C>T (p.Ala486Val) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73323418G>C | CA393088438 | HCN4 | c.2675C>G (p.Ala892Gly) c.1457C>G (p.Ala486Gly) | |
| 15 | g.73323418G= | CA2187188240 | HCN4 | c.2675C= (p.Ala892=) c.1457C= (p.Ala486=) | |
| 15 | g.73323418G>T | CA393088439 | HCN4 | c.2675C>A (p.Ala892Asp) c.1457C>A (p.Ala486Asp) | |
| 15 | g.73323419C>A | CA393088440 | HCN4 | c.2674G>T (p.Ala892Ser) c.1456G>T (p.Ala486Ser) | |
| 15 | g.73323419C>G | CA393088441 | HCN4 | c.2674G>C (p.Ala892Pro) c.1456G>C (p.Ala486Pro) | |
| 15 | g.73323419C>T | CA393088442 | HCN4 | c.2674G>A (p.Ala892Thr) c.1456G>A (p.Ala486Thr) | gnomAD v4 |
| 15 | g.73323420C>A | CA491478556 | HCN4 | c.2673G>T (p.Ser891=) c.1455G>T (p.Ser485=) | |
| 15 | g.73323420C= | CA2187188245 | HCN4 | c.2673G= (p.Ser891=) c.1455G= (p.Ser485=) | |
| 15 | g.73323420C>G | CA491478559 | HCN4 | c.2673G>C (p.Ser891=) c.1455G>C (p.Ser485=) | dbSNP gnomAD v4 |
| 15 | g.73323420C>T | CA350593 | HCN4 | c.2673G>A (p.Ser891=) c.1455G>A (p.Ser485=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323421G>A | CA7648972 | HCN4 | c.2672C>T (p.Ser891Leu) c.1454C>T (p.Ser485Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323421G>C | CA7648973 | HCN4 | c.2672C>G (p.Ser891Trp) c.1454C>G (p.Ser485Trp) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323421G= | CA2187188250 | HCN4 | c.2672C= (p.Ser891=) c.1454C= (p.Ser485=) | |
| 15 | g.73323421G>T | CA393088443 | HCN4 | c.2672C>A (p.Ser891Ter) c.1454C>A (p.Ser485Ter) | gnomAD v4 |
| 15 | g.73323422A>C | CA393088446 | HCN4 | c.2671T>G (p.Ser891Ala) c.1453T>G (p.Ser485Ala) | |
| 15 | g.73323422A>G | CA393088445 | HCN4 | c.2671T>C (p.Ser891Pro) c.1453T>C (p.Ser485Pro) | |
| 15 | g.73323422A>T | CA393088444 | HCN4 | c.2671T>A (p.Ser891Thr) c.1453T>A (p.Ser485Thr) | |
| 15 | g.73323423G>A | CA491478574 | HCN4 | c.2670C>T (p.Pro890=) c.1452C>T (p.Pro484=) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73323423G>C | CA491478568 | HCN4 | c.2670C>G (p.Pro890=) c.1452C>G (p.Pro484=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323423G= | CA2187188257 | HCN4 | c.2670C= (p.Pro890=) c.1452C= (p.Pro484=) | |
| 15 | g.73323423G>T | CA491478571 | HCN4 | c.2670C>A (p.Pro890=) c.1452C>A (p.Pro484=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323427del | CA2575783833 | HCN4 | c.2670del (p.Ser891ArgfsTer9) c.1452del (p.Ser485ArgfsTer9) | gnomAD v4 |
| 15 | g.73323424G>A | CA7648974 | HCN4 | c.2669C>T (p.Pro890Leu) c.1451C>T (p.Pro484Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.73323424G>C | CA393088447 | HCN4 | c.2669C>G (p.Pro890Arg) c.1451C>G (p.Pro484Arg) | |
| 15 | g.73323424G= | CA2187188261 | HCN4 | c.2669C= (p.Pro890=) c.1451C= (p.Pro484=) | |
| 15 | g.73323424G>T | CA393088448 | HCN4 | c.2669C>A (p.Pro890His) c.1451C>A (p.Pro484His) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323425G>A | CA7648975 | HCN4 | c.2668C>T (p.Pro890Ser) c.1450C>T (p.Pro484Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.73323425G>C | CA393088449 | HCN4 | c.2668C>G (p.Pro890Ala) c.1450C>G (p.Pro484Ala) | ClinVar dbSNP |
| 15 | g.73323425G= | CA2187188270 | HCN4 | c.2668C= (p.Pro890=) c.1450C= (p.Pro484=) | |
| 15 | g.73323425G>T | CA393088450 | HCN4 | c.2668C>A (p.Pro890Thr) c.1450C>A (p.Pro484Thr) | |
| 15 | g.73323426G>A | CA491478586 | HCN4 | c.2667C>T (p.Ser889=) c.1449C>T (p.Ser483=) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73323426G>C | CA491478583 | HCN4 | c.2667C>G (p.Ser889=) c.1449C>G (p.Ser483=) | |
| 15 | g.73323426G>T | CA491478580 | HCN4 | c.2667C>A (p.Ser889=) c.1449C>A (p.Ser483=) | gnomAD v4 |
| 15 | g.73323427G>A | CA7648976 | HCN4 | c.2666C>T (p.Ser889Phe) c.1448C>T (p.Ser483Phe) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323427G>C | CA393088451 | HCN4 | c.2666C>G (p.Ser889Cys) c.1448C>G (p.Ser483Cys) | |
| 15 | g.73323427G= | CA2187188275 | HCN4 | c.2666C= (p.Ser889=) c.1448C= (p.Ser483=) | |
| 15 | g.73323427G>T | CA393088452 | HCN4 | c.2666C>A (p.Ser889Tyr) c.1448C>A (p.Ser483Tyr) | |
| 15 | g.73323428A>C | CA393088453 | HCN4 | c.2665T>G (p.Ser889Ala) c.1447T>G (p.Ser483Ala) | |
| 15 | g.73323428A>G | CA393088454 | HCN4 | c.2665T>C (p.Ser889Pro) c.1447T>C (p.Ser483Pro) | dbSNP gnomAD v4 |
| 15 | g.73323428A>T | CA393088455 | HCN4 | c.2665T>A (p.Ser889Thr) c.1447T>A (p.Ser483Thr) | gnomAD v4 |
| 15 | g.73323429G>A | CA491478587 | HCN4 | c.2664C>T (p.Gly888=) c.1446C>T (p.Gly482=) | gnomAD v4 |
| 15 | g.73323429G>C | CA491478591 | HCN4 | c.2664C>G (p.Gly888=) c.1446C>G (p.Gly482=) | |
| 15 | g.73323429G>T | CA491478588 | HCN4 | c.2664C>A (p.Gly888=) c.1446C>A (p.Gly482=) | gnomAD v4 |
| 15 | g.73323430C>A | CA393088458 | HCN4 | c.2663G>T (p.Gly888Val) c.1445G>T (p.Gly482Val) | |
| 15 | g.73323430C= | CA2187188279 | HCN4 | c.2663G= (p.Gly888=) c.1445G= (p.Gly482=) | |
| 15 | g.73323430C>G | CA393088457 | HCN4 | c.2663G>C (p.Gly888Ala) c.1445G>C (p.Gly482Ala) | |
| 15 | g.73323430C>T | CA393088456 | HCN4 | c.2663G>A (p.Gly888Asp) c.1445G>A (p.Gly482Asp) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323431C>A | CA393088459 | HCN4 | c.2662G>T (p.Gly888Cys) c.1444G>T (p.Gly482Cys) | |
| 15 | g.73323431C= | CA2187188283 | HCN4 | c.2662G= (p.Gly888=) c.1444G= (p.Gly482=) | |
| 15 | g.73323431C>G | CA393088461 | HCN4 | c.2662G>C (p.Gly888Arg) c.1444G>C (p.Gly482Arg) | |
| 15 | g.73323431C>T | CA393088460 | HCN4 | c.2662G>A (p.Gly888Ser) c.1444G>A (p.Gly482Ser) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73323432A>C | CA393088462 | HCN4 | c.2661T>G (p.Cys887Trp) c.1443T>G (p.Cys481Trp) | |
| 15 | g.73323432A>G | CA491478597 | HCN4 | c.2661T>C (p.Cys887=) c.1443T>C (p.Cys481=) | |
| 15 | g.73323432A>T | CA393088463 | HCN4 | c.2661T>A (p.Cys887Ter) c.1443T>A (p.Cys481Ter) | |
| 15 | g.73323433C>A | CA393088464 | HCN4 | c.2660G>T (p.Cys887Phe) c.1442G>T (p.Cys481Phe) | |
| 15 | g.73323433C= | CA2187188286 | HCN4 | c.2660G= (p.Cys887=) c.1442G= (p.Cys481=) | |
| 15 | g.73323433C>G | CA393088465 | HCN4 | c.2660G>C (p.Cys887Ser) c.1442G>C (p.Cys481Ser) | |
| 15 | g.73323433C>T | CA7648977 | HCN4 | c.2660G>A (p.Cys887Tyr) c.1442G>A (p.Cys481Tyr) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323434A>C | CA393088466 | HCN4 | c.2659T>G (p.Cys887Gly) c.1441T>G (p.Cys481Gly) | |
| 15 | g.73323434A>G | CA393088467 | HCN4 | c.2659T>C (p.Cys887Arg) c.1441T>C (p.Cys481Arg) | gnomAD v4 |
| 15 | g.73323434A>T | CA393088468 | HCN4 | c.2659T>A (p.Cys887Ser) c.1441T>A (p.Cys481Ser) | |
| 15 | g.73323435G>A | CA491478608 | HCN4 | c.2658C>T (p.Ala886=) c.1440C>T (p.Ala480=) | |
| 15 | g.73323435G>C | CA491478610 | HCN4 | c.2658C>G (p.Ala886=) c.1440C>G (p.Ala480=) | gnomAD v4 |
| 15 | g.73323435G>T | CA491478612 | HCN4 | c.2658C>A (p.Ala886=) c.1440C>A (p.Ala480=) | gnomAD v4 |
| 15 | g.73323436G>A | CA203631 | HCN4 | c.2657C>T (p.Ala886Val) c.1439C>T (p.Ala480Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323436G>C | CA272664390 | HCN4 | c.2657C>G (p.Ala886Gly) c.1439C>G (p.Ala480Gly) | dbSNP |
| 15 | g.73323436G= | CA2187188290 | HCN4 | c.2657C= (p.Ala886=) c.1439C= (p.Ala480=) | |
| 15 | g.73323436G>T | CA393088469 | HCN4 | c.2657C>A (p.Ala886Asp) c.1439C>A (p.Ala480Asp) | gnomAD v4 |
| 15 | g.73323437C>A | CA393088470 | HCN4 | c.2656G>T (p.Ala886Ser) c.1438G>T (p.Ala480Ser) | |
| 15 | g.73323437C>G | CA393088471 | HCN4 | c.2656G>C (p.Ala886Pro) c.1438G>C (p.Ala480Pro) | |
| 15 | g.73323437C>T | CA393088472 | HCN4 | c.2656G>A (p.Ala886Thr) c.1438G>A (p.Ala480Thr) | gnomAD v4 |
| 15 | g.73323438C>A | CA7648978 | HCN4 | c.2655G>T (p.Gly885=) c.1437G>T (p.Gly479=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323438C= | CA2187188292 | HCN4 | c.2655G= (p.Gly885=) c.1437G= (p.Gly479=) | |
| 15 | g.73323438C>G | CA491478619 | HCN4 | c.2655G>C (p.Gly885=) c.1437G>C (p.Gly479=) | |
| 15 | g.73323438C>T | CA491478621 | HCN4 | c.2655G>A (p.Gly885=) c.1437G>A (p.Gly479=) | gnomAD v4 COSMIC |
| 15 | g.73323439C>A | CA393088473 | HCN4 | c.2654G>T (p.Gly885Val) c.1436G>T (p.Gly479Val) | |
| 15 | g.73323439C>G | CA393088474 | HCN4 | c.2654G>C (p.Gly885Ala) c.1436G>C (p.Gly479Ala) | |
| 15 | g.73323439C>T | CA393088475 | HCN4 | c.2654G>A (p.Gly885Glu) c.1436G>A (p.Gly479Glu) | |
| 15 | g.73323440C>A | CA393088477 | HCN4 | c.2653G>T (p.Gly885Trp) c.1435G>T (p.Gly479Trp) | |
| 15 | g.73323440C= | CA2187188295 | HCN4 | c.2653G= (p.Gly885=) c.1435G= (p.Gly479=) | |
| 15 | g.73323440C>G | CA393088476 | HCN4 | c.2653G>C (p.Gly885Arg) c.1435G>C (p.Gly479Arg) | ClinVar dbSNP |
| 15 | g.73323440C>T | CA7648979 | HCN4 | c.2653G>A (p.Gly885Arg) c.1435G>A (p.Gly479Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.73323441G>A | CA7648980 | HCN4 | c.2652C>T (p.Pro884=) c.1434C>T (p.Pro478=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.73323441G>C | CA491478630 | HCN4 | c.2652C>G (p.Pro884=) c.1434C>G (p.Pro478=) | |
| 15 | g.73323441G= | CA2187188297 | HCN4 | c.2652C= (p.Pro884=) c.1434C= (p.Pro478=) | |
| 15 | g.73323441G>T | CA491478631 | HCN4 | c.2652C>A (p.Pro884=) c.1434C>A (p.Pro478=) | gnomAD v4 |
| 15 | g.73323446dup | CA619410590 | HCN4 | c.2652dup (p.Gly885ArgfsTer?) c.1434dup (p.Gly479ArgfsTer?) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 15 | g.73323446del | CA2629370567 | HCN4 | c.2652del (p.Ala886ProfsTer14) c.1434del (p.Ala480ProfsTer14) | gnomAD v4 |
| 15 | g.73323442G>A | CA393088478 | HCN4 | c.2651C>T (p.Pro884Leu) c.1433C>T (p.Pro478Leu) | gnomAD v4 |
| 15 | g.73323442G>C | CA393088479 | HCN4 | c.2651C>G (p.Pro884Arg) c.1433C>G (p.Pro478Arg) | |
| 15 | g.73323442G>T | CA393088480 | HCN4 | c.2651C>A (p.Pro884His) c.1433C>A (p.Pro478His) | |
| 15 | g.73323443G>A | CA7648981 | HCN4 | c.2650C>T (p.Pro884Ser) c.1432C>T (p.Pro478Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323443G>C | CA272664429 | HCN4 | c.2650C>G (p.Pro884Ala) c.1432C>G (p.Pro478Ala) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323443G= | CA2187188302 | HCN4 | c.2650C= (p.Pro884=) c.1432C= (p.Pro478=) | |
| 15 | g.73323443G>T | CA272664436 | HCN4 | c.2650C>A (p.Pro884Thr) c.1432C>A (p.Pro478Thr) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323444G>A | CA491478639 | HCN4 | c.2649C>T (p.Pro883=) c.1431C>T (p.Pro477=) | |
| 15 | g.73323444G>C | CA491478641 | HCN4 | c.2649C>G (p.Pro883=) c.1431C>G (p.Pro477=) | dbSNP gnomAD v4 |
| 15 | g.73323444G= | CA2187188305 | HCN4 | c.2649C= (p.Pro883=) c.1431C= (p.Pro477=) | |
| 15 | g.73323444G>T | CA491478640 | HCN4 | c.2649C>A (p.Pro883=) c.1431C>A (p.Pro477=) | gnomAD v4 |
| 15 | g.73323445G>A | CA393088481 | HCN4 | c.2648C>T (p.Pro883Leu) c.1430C>T (p.Pro477Leu) | |
| 15 | g.73323445G>C | CA163178 | HCN4 | c.2648C>G (p.Pro883Arg) c.1430C>G (p.Pro477Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323445G= | CA2187188311 | HCN4 | c.2648C= (p.Pro883=) c.1430C= (p.Pro477=) | |
| 15 | g.73323445G>T | CA393088482 | HCN4 | c.2648C>A (p.Pro883His) c.1430C>A (p.Pro477His) | gnomAD v4 |
| 15 | g.73323446G>A | CA7648982 | HCN4 | c.2647C>T (p.Pro883Ser) c.1429C>T (p.Pro477Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 15 | g.73323446G>C | CA393088483 | HCN4 | c.2647C>G (p.Pro883Ala) c.1429C>G (p.Pro477Ala) | |
| 15 | g.73323446G= | CA2187188315 | HCN4 | c.2647C= (p.Pro883=) c.1429C= (p.Pro477=) | |
| 15 | g.73323446G>T | CA393088484 | HCN4 | c.2647C>A (p.Pro883Thr) c.1429C>A (p.Pro477Thr) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323447T>A | CA491478648 | HCN4 | c.2646A>T (p.Pro882=) c.1428A>T (p.Pro476=) | |
| 15 | g.73323447T>C | CA491478650 | HCN4 | c.2646A>G (p.Pro882=) c.1428A>G (p.Pro476=) | gnomAD v4 |
| 15 | g.73323447T>G | CA491478649 | HCN4 | c.2646A>C (p.Pro882=) c.1428A>C (p.Pro476=) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73323447T= | CA2187188318 | HCN4 | c.2646A= (p.Pro882=) c.1428A= (p.Pro476=) | |
| 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.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 |