| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 15 | g.73323092G>A | CA393086489 | HCN4 | c.3001C>T (p.Pro1001Ser) c.1783C>T (p.Pro595Ser) | gnomAD v4 |
| 15 | g.73323092G>C | CA393086491 | HCN4 | c.3001C>G (p.Pro1001Ala) c.1783C>G (p.Pro595Ala) | |
| 15 | g.73323092G>T | CA393086492 | HCN4 | c.3001C>A (p.Pro1001Thr) c.1783C>A (p.Pro595Thr) | ClinVar gnomAD v4 |
| 15 | g.73323093C>A | CA393086494 | HCN4 | c.3000G>T (p.Gln1000His) c.1782G>T (p.Gln594His) | gnomAD v4 |
| 15 | g.73323093C>G | CA393086495 | HCN4 | c.3000G>C (p.Gln1000His) c.1782G>C (p.Gln594His) | |
| 15 | g.73323093C>T | CA491478508 | HCN4 | c.3000G>A (p.Gln1000=) c.1782G>A (p.Gln594=) | gnomAD v4 |
| 15 | g.73323094T>A | CA393086500 | HCN4 | c.2999A>T (p.Gln1000Leu) c.1781A>T (p.Gln594Leu) | |
| 15 | g.73323094T>C | CA393086499 | HCN4 | c.2999A>G (p.Gln1000Arg) c.1781A>G (p.Gln594Arg) | |
| 15 | g.73323094T>G | CA393086497 | HCN4 | c.2999A>C (p.Gln1000Pro) c.1781A>C (p.Gln594Pro) | |
| 15 | g.73323095G>A | CA393086502 | HCN4 | c.2998C>T (p.Gln1000Ter) c.1780C>T (p.Gln594Ter) | gnomAD v4 |
| 15 | g.73323095G>C | CA393086504 | HCN4 | c.2998C>G (p.Gln1000Glu) c.1780C>G (p.Gln594Glu) | |
| 15 | g.73323095G= | CA2187187474 | HCN4 | c.2998C= (p.Gln1000=) c.1780C= (p.Gln594=) | |
| 15 | g.73323095G>T | CA393086506 | HCN4 | c.2998C>A (p.Gln1000Lys) c.1780C>A (p.Gln594Lys) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323096C>A | CA491478517 | HCN4 | c.2997G>T (p.Arg999=) c.1779G>T (p.Arg593=) | gnomAD v4 |
| 15 | g.73323096C= | CA2187187481 | HCN4 | c.2997G= (p.Arg999=) c.1779G= (p.Arg593=) | |
| 15 | g.73323096C>G | CA7648907 | HCN4 | c.2997G>C (p.Arg999=) c.1779G>C (p.Arg593=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323096C>T | CA7648908 | HCN4 | c.2997G>A (p.Arg999=) c.1779G>A (p.Arg593=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323097C>A | CA393086514 | HCN4 | c.2996G>T (p.Arg999Leu) c.1778G>T (p.Arg593Leu) | gnomAD v4 |
| 15 | g.73323097C= | CA2187187487 | HCN4 | c.2996G= (p.Arg999=) c.1778G= (p.Arg593=) | |
| 15 | g.73323097C>G | CA393086516 | HCN4 | c.2996G>C (p.Arg999Pro) c.1778G>C (p.Arg593Pro) | |
| 15 | g.73323097C>T | CA393086517 | HCN4 | c.2996G>A (p.Arg999Gln) c.1778G>A (p.Arg593Gln) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323098G>A | CA272663979 | HCN4 | c.2995C>T (p.Arg999Trp) c.1777C>T (p.Arg593Trp) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.73323098G>C | CA393086522 | HCN4 | c.2995C>G (p.Arg999Gly) c.1777C>G (p.Arg593Gly) | |
| 15 | g.73323098G= | CA2187187494 | HCN4 | c.2995C= (p.Arg999=) c.1777C= (p.Arg593=) | |
| 15 | g.73323098G>T | CA491478524 | HCN4 | c.2995C>A (p.Arg999=) c.1777C>A (p.Arg593=) | gnomAD v4 |
| 15 | g.73323099T>A | CA491478526 | HCN4 | c.2994A>T (p.Pro998=) c.1776A>T (p.Pro592=) | |
| 15 | g.73323099T>C | CA491478527 | HCN4 | c.2994A>G (p.Pro998=) c.1776A>G (p.Pro592=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323099T>G | CA491478528 | HCN4 | c.2994A>C (p.Pro998=) c.1776A>C (p.Pro592=) | |
| 15 | g.73323099T= | CA2187187499 | HCN4 | c.2994A= (p.Pro998=) c.1776A= (p.Pro592=) | |
| 15 | g.73323100G>A | CA7648909 | HCN4 | c.2993C>T (p.Pro998Leu) c.1775C>T (p.Pro592Leu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323100G>C | CA393086525 | HCN4 | c.2993C>G (p.Pro998Arg) c.1775C>G (p.Pro592Arg) | |
| 15 | g.73323100G= | CA2187187502 | HCN4 | c.2993C= (p.Pro998=) c.1775C= (p.Pro592=) | |
| 15 | g.73323100G>T | CA393086528 | HCN4 | c.2993C>A (p.Pro998Gln) c.1775C>A (p.Pro592Gln) | gnomAD v4 |
| 15 | g.73323104del | CA491478535 | HCN4 | c.2993del (p.Pro998HisfsTer20) c.1775del (p.Pro592HisfsTer20) | gnomAD v4 COSMIC |
| 15 | g.73323101G>A | CA393086536 | HCN4 | c.2992C>T (p.Pro998Ser) c.1774C>T (p.Pro592Ser) | gnomAD v4 |
| 15 | g.73323101G>C | CA7648910 | HCN4 | c.2992C>G (p.Pro998Ala) c.1774C>G (p.Pro592Ala) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323101G= | CA2187187504 | HCN4 | c.2992C= (p.Pro998=) c.1774C= (p.Pro592=) | |
| 15 | g.73323101G>T | CA393086534 | HCN4 | c.2992C>A (p.Pro998Thr) c.1774C>A (p.Pro592Thr) | gnomAD v4 |
| 15 | g.73323102G>A | CA491478537 | HCN4 | c.2991C>T (p.Pro997=) c.1773C>T (p.Pro591=) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323102G>C | CA491478539 | HCN4 | c.2991C>G (p.Pro997=) c.1773C>G (p.Pro591=) | gnomAD v4 |
| 15 | g.73323102G= | CA2187187506 | HCN4 | c.2991C= (p.Pro997=) c.1773C= (p.Pro591=) | |
| 15 | g.73323102G>T | CA491478540 | HCN4 | c.2991C>A (p.Pro997=) c.1773C>A (p.Pro591=) | |
| 15 | g.73323103G>A | CA393086539 | HCN4 | c.2990C>T (p.Pro997Leu) c.1772C>T (p.Pro591Leu) | gnomAD v4 |
| 15 | g.73323103G>C | CA393086541 | HCN4 | c.2990C>G (p.Pro997Arg) c.1772C>G (p.Pro591Arg) | |
| 15 | g.73323103G= | CA2187187511 | HCN4 | c.2990C= (p.Pro997=) c.1772C= (p.Pro591=) | |
| 15 | g.73323103G>T | CA272663982 | HCN4 | c.2990C>A (p.Pro997His) c.1772C>A (p.Pro591His) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323104G>A | CA393086551 | HCN4 | c.2989C>T (p.Pro997Ser) c.1771C>T (p.Pro591Ser) | gnomAD v4 |
| 15 | g.73323104G>C | CA393086554 | HCN4 | c.2989C>G (p.Pro997Ala) c.1771C>G (p.Pro591Ala) | |
| 15 | g.73323104G= | CA2187187516 | HCN4 | c.2989C= (p.Pro997=) c.1771C= (p.Pro591=) | |
| 15 | g.73323104G>T | CA7648911 | HCN4 | c.2989C>A (p.Pro997Thr) c.1771C>A (p.Pro591Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |