| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 15 | g.73322579C>A | CA393085045 | HCN4 | c.3514G>T (p.Ala1172Ser) c.2296G>T (p.Ala766Ser) | |
| 15 | g.73322579C>G | CA393085047 | HCN4 | c.3514G>C (p.Ala1172Pro) c.2296G>C (p.Ala766Pro) | |
| 15 | g.73322579C>T | CA393085049 | HCN4 | c.3514G>A (p.Ala1172Thr) c.2296G>A (p.Ala766Thr) | gnomAD v4 |
| 15 | g.73322580T>A | CA393085051 | HCN4 | c.3513A>T (p.Arg1171Ser) c.2295A>T (p.Arg765Ser) | |
| 15 | g.73322580T>C | CA491477930 | HCN4 | c.3513A>G (p.Arg1171=) c.2295A>G (p.Arg765=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73322580T>G | CA393085052 | HCN4 | c.3513A>C (p.Arg1171Ser) c.2295A>C (p.Arg765Ser) | gnomAD v4 |
| 15 | g.73322580T= | CA2187186274 | HCN4 | c.3513A= (p.Arg1171=) c.2295A= (p.Arg765=) | |
| 15 | g.73322581C>A | CA301975 | HCN4 | c.3512G>T (p.Arg1171Ile) c.2294G>T (p.Arg765Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73322581C= | CA2187186281 | HCN4 | c.3512G= (p.Arg1171=) c.2294G= (p.Arg765=) | |
| 15 | g.73322581C>G | CA393085054 | HCN4 | c.3512G>C (p.Arg1171Thr) c.2294G>C (p.Arg765Thr) | |
| 15 | g.73322581C>T | CA393085055 | HCN4 | c.3512G>A (p.Arg1171Lys) c.2294G>A (p.Arg765Lys) | ClinVar dbSNP gnomAD v4 COSMIC |
| 15 | g.73322582T>A | CA393085056 | HCN4 | c.3511A>T (p.Arg1171Ter) c.2293A>T (p.Arg765Ter) | |
| 15 | g.73322582T>C | CA393085057 | HCN4 | c.3511A>G (p.Arg1171Gly) c.2293A>G (p.Arg765Gly) | |
| 15 | g.73322582T>G | CA491477934 | HCN4 | c.3511A>C (p.Arg1171=) c.2293A>C (p.Arg765=) | |
| 15 | g.73322583T>A | CA491477937 | HCN4 | c.3510A>T (p.Ala1170=) c.2292A>T (p.Ala764=) | |
| 15 | g.73322583T>C | CA491477935 | HCN4 | c.3510A>G (p.Ala1170=) c.2292A>G (p.Ala764=) | |
| 15 | g.73322583T>G | CA491477936 | HCN4 | c.3510A>C (p.Ala1170=) c.2292A>C (p.Ala764=) | |
| 15 | g.73322584G>A | CA393085062 | HCN4 | c.3509C>T (p.Ala1170Val) c.2291C>T (p.Ala764Val) | |
| 15 | g.73322584G>C | CA393085060 | HCN4 | c.3509C>G (p.Ala1170Gly) c.2291C>G (p.Ala764Gly) | |
| 15 | g.73322584G>T | CA393085059 | HCN4 | c.3509C>A (p.Ala1170Glu) c.2291C>A (p.Ala764Glu) | |
| 15 | g.73322585C>A | CA393085064 | HCN4 | c.3508G>T (p.Ala1170Ser) c.2290G>T (p.Ala764Ser) | |
| 15 | g.73322585C= | CA2187186285 | HCN4 | c.3508G= (p.Ala1170=) c.2290G= (p.Ala764=) | |
| 15 | g.73322585C>G | CA393085067 | HCN4 | c.3508G>C (p.Ala1170Pro) c.2290G>C (p.Ala764Pro) | |
| 15 | g.73322585C>T | CA393085066 | HCN4 | c.3508G>A (p.Ala1170Thr) c.2290G>A (p.Ala764Thr) | dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 15 | g.73322586C>A | CA491477939 | HCN4 | c.3507G>T (p.Gly1169=) c.2289G>T (p.Gly763=) | |
| 15 | g.73322586C>G | CA491477940 | HCN4 | c.3507G>C (p.Gly1169=) c.2289G>C (p.Gly763=) | |
| 15 | g.73322586C>T | CA491477941 | HCN4 | c.3507G>A (p.Gly1169=) c.2289G>A (p.Gly763=) | COSMIC |
| 15 | g.73322587C>A | CA393085069 | HCN4 | c.3506G>T (p.Gly1169Val) c.2288G>T (p.Gly763Val) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73322587C= | CA2187186289 | HCN4 | c.3506G= (p.Gly1169=) c.2288G= (p.Gly763=) | |
| 15 | g.73322587C>G | CA393085070 | HCN4 | c.3506G>C (p.Gly1169Ala) c.2288G>C (p.Gly763Ala) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73322587C>T | CA393085071 | HCN4 | c.3506G>A (p.Gly1169Glu) c.2288G>A (p.Gly763Glu) | |
| 15 | g.73322587_73322590del | CA2629370523 | HCN4 | c.3503_3506del (p.Phe1168TrpfsTer12) c.2285_2288del (p.Phe762TrpfsTer12) | gnomAD v4 |
| 15 | g.73322587_73322591delinsCCAAA | CA2187186288 | HCN4 | c.3502_3506delinsTTTGG (p.Phe1168=) c.2284_2288delinsTTTGG (p.Phe762=) | |
| 15 | g.73322588C>A | CA393085076 | HCN4 | c.3505G>T (p.Gly1169Trp) c.2287G>T (p.Gly763Trp) | |
| 15 | g.73322588C>G | CA393085077 | HCN4 | c.3505G>C (p.Gly1169Arg) c.2287G>C (p.Gly763Arg) | |
| 15 | g.73322588C>T | CA393085078 | HCN4 | c.3505G>A (p.Gly1169Arg) c.2287G>A (p.Gly763Arg) | |
| 15 | g.73322588_73322594delinsCAAACAA | CA2187186298 | HCN4 | c.3499_3505delinsTTGTTTG (p.Leu1167=) c.2281_2287delinsTTGTTTG (p.Leu761=) | |
| 15 | g.73322592_73322595del | CA199790 | HCN4 | c.3502_3505del (p.Phe1168GlyfsTer12) c.2284_2287del (p.Phe762GlyfsTer12) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73322589A= | CA2187186302 | HCN4 | c.3504T= (p.Phe1168=) c.2286T= (p.Phe762=) | |
| 15 | g.73322589A>C | CA393085082 | HCN4 | c.3504T>G (p.Phe1168Leu) c.2286T>G (p.Phe762Leu) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73322589A>G | CA491477943 | HCN4 | c.3504T>C (p.Phe1168=) c.2286T>C (p.Phe762=) | |
| 15 | g.73322589A>T | CA393085085 | HCN4 | c.3504T>A (p.Phe1168Leu) c.2286T>A (p.Phe762Leu) | |
| 15 | g.73322590_73322595del | CA619410585 | HCN4 | c.3499_3504del (p.Leu1167_Phe1168del) c.2281_2286del (p.Leu761_Phe762del) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73322590A= | CA2187186304 | HCN4 | c.3503T= (p.Phe1168=) c.2285T= (p.Phe762=) | |
| 15 | g.73322590A>C | CA393085091 | HCN4 | c.3503T>G (p.Phe1168Cys) c.2285T>G (p.Phe762Cys) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73322590A>G | CA393085090 | HCN4 | c.3503T>C (p.Phe1168Ser) c.2285T>C (p.Phe762Ser) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73322590A>T | CA393085088 | HCN4 | c.3503T>A (p.Phe1168Tyr) c.2285T>A (p.Phe762Tyr) | |
| 15 | g.73322591A>C | CA393085093 | HCN4 | c.3502T>G (p.Phe1168Val) c.2284T>G (p.Phe762Val) | |
| 15 | g.73322591A>G | CA393085095 | HCN4 | c.3502T>C (p.Phe1168Leu) c.2284T>C (p.Phe762Leu) | |
| 15 | g.73322591A>T | CA393085097 | HCN4 | c.3502T>A (p.Phe1168Ile) c.2284T>A (p.Phe762Ile) |