Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.73367722C>A | CA7649463 | HCN4 | c.549G>T (p.Ser183=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73367722C= | CA2187194520 | HCN4 | c.549G= (p.Ser183=) | |
15 | g.73367722C>G | CA491479559 | HCN4 | c.549G>C (p.Ser183=) | |
15 | g.73367722C>T | CA491479560 | HCN4 | c.549G>A (p.Ser183=) | gnomAD v4 |
15 | g.73367723G>A | CA272700245 | HCN4 | c.548C>T (p.Ser183Leu) | dbSNP gnomAD v4 |
15 | g.73367723G>C | CA393097674 | HCN4 | c.548C>G (p.Ser183Trp) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
15 | g.73367723G= | CA2187194521 | HCN4 | c.548C= (p.Ser183=) | |
15 | g.73367723G>T | CA393097676 | HCN4 | c.548C>A (p.Ser183Ter) | |
15 | g.73367724A>C | CA393097679 | HCN4 | c.547T>G (p.Ser183Ala) | |
15 | g.73367724A>G | CA393097678 | HCN4 | c.547T>C (p.Ser183Pro) | |
15 | g.73367724A>T | CA393097677 | HCN4 | c.547T>A (p.Ser183Thr) | |
15 | g.73367725G>A | CA491479561 | HCN4 | c.546C>T (p.Pro182=) | ClinVar dbSNP gnomAD v4 |
15 | g.73367725G>C | CA7649464 | HCN4 | c.546C>G (p.Pro182=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
15 | g.73367725G= | CA2187194522 | HCN4 | c.546C= (p.Pro182=) | |
15 | g.73367725G>T | CA491479562 | HCN4 | c.546C>A (p.Pro182=) | |
15 | g.73367727del | CA2629389814 | HCN4 | c.546del (p.Ser183ArgfsTer?) | gnomAD v4 |
15 | g.73367726G>A | CA7649465 | HCN4 | c.545C>T (p.Pro182Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73367726G>C | CA393097681 | HCN4 | c.545C>G (p.Pro182Arg) | |
15 | g.73367726G= | CA2187194523 | HCN4 | c.545C= (p.Pro182=) | |
15 | g.73367726G>T | CA393097683 | HCN4 | c.545C>A (p.Pro182His) | |
15 | g.73367732_73367755dup | CA2629389815 | HCN4 | c.522_545dup (p.Pro182_Ser183insAlaSerAlaSerCysGluGlnPro) | gnomAD v4 |
15 | g.73367727G>A | CA393097685 | HCN4 | c.544C>T (p.Pro182Ser) | gnomAD v4 |
15 | g.73367727G>C | CA393097687 | HCN4 | c.544C>G (p.Pro182Ala) | |
15 | g.73367727G>T | CA393097688 | HCN4 | c.544C>A (p.Pro182Thr) | |
15 | g.73367728C>A | CA393097689 | HCN4 | c.543G>T (p.Gln181His) | gnomAD v4 |
15 | g.73367728C>G | CA393097691 | HCN4 | c.543G>C (p.Gln181His) | |
15 | g.73367728C>T | CA491479563 | HCN4 | c.543G>A (p.Gln181=) | dbSNP gnomAD v4 |
15 | g.73367729T>A | CA393097693 | HCN4 | c.542A>T (p.Gln181Leu) | ClinVar dbSNP |
15 | g.73367729T>C | CA393097695 | HCN4 | c.542A>G (p.Gln181Arg) | |
15 | g.73367729T>G | CA393097696 | HCN4 | c.542A>C (p.Gln181Pro) | |
15 | g.73367729T= | CA2187194524 | HCN4 | c.542A= (p.Gln181=) | |
15 | g.73367730G>A | CA393097699 | HCN4 | c.541C>T (p.Gln181Ter) | gnomAD v4 |
15 | g.73367730G>C | CA393097698 | HCN4 | c.541C>G (p.Gln181Glu) | ClinVar dbSNP |
15 | g.73367730G>T | CA393097697 | HCN4 | c.541C>A (p.Gln181Lys) | gnomAD v4 |
15 | g.73367731C>A | CA393097700 | HCN4 | c.540G>T (p.Glu180Asp) | |
15 | g.73367731C>G | CA393097702 | HCN4 | c.540G>C (p.Glu180Asp) | |
15 | g.73367731C>T | CA491479564 | HCN4 | c.540G>A (p.Glu180=) | |
15 | g.73367732T>A | CA393097703 | HCN4 | c.539A>T (p.Glu180Val) | |
15 | g.73367732T>C | CA393097704 | HCN4 | c.539A>G (p.Glu180Gly) | |
15 | g.73367732T>G | CA7649466 | HCN4 | c.539A>C (p.Glu180Ala) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73367732T= | CA2187194525 | HCN4 | c.539A= (p.Glu180=) | |
15 | g.73367733C>A | CA393097706 | HCN4 | c.538G>T (p.Glu180Ter) | dbSNP COSMIC |
15 | g.73367733C= | CA2187194526 | HCN4 | c.538G= (p.Glu180=) | |
15 | g.73367733C>G | CA393097707 | HCN4 | c.538G>C (p.Glu180Gln) | |
15 | g.73367733C>T | CA393097709 | HCN4 | c.538G>A (p.Glu180Lys) | COSMIC |
15 | g.73367734G>A | CA7649467 | HCN4 | c.537C>T (p.Cys179=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73367734G>C | CA393097710 | HCN4 | c.537C>G (p.Cys179Trp) | dbSNP gnomAD v3 gnomAD v4 |
15 | g.73367734G= | CA2187194527 | HCN4 | c.537C= (p.Cys179=) | |
15 | g.73367734G>T | CA393097712 | HCN4 | c.537C>A (p.Cys179Ter) | |
15 | g.73367735C>A | CA393097714 | HCN4 | c.536G>T (p.Cys179Phe) |