| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 5 | g.45645575C>A | CA359707866 | HCN1 | c.459G>T (p.Met153Ile) | ClinVar |
| 5 | g.45645575C= | CA1543790783 | HCN1 | c.459G= (p.Met153=) | |
| 5 | g.45645575C>G | CA16044318 | HCN1 | c.459G>C (p.Met153Ile) | ClinVar dbSNP |
| 5 | g.45645575C>T | CA359707867 | HCN1 | c.459G>A (p.Met153Ile) | |
| 5 | g.45645576A>C | CA359707868 | HCN1 | c.458T>G (p.Met153Arg) | |
| 5 | g.45645576A>G | CA359707869 | HCN1 | c.458T>C (p.Met153Thr) | dbSNP COSMIC |
| 5 | g.45645576A>T | CA359707870 | HCN1 | c.458T>A (p.Met153Lys) | |
| 5 | g.45645577T>A | CA359707871 | HCN1 | c.457A>T (p.Met153Leu) | |
| 5 | g.45645577T>C | CA359707872 | HCN1 | c.457A>G (p.Met153Val) | dbSNP gnomAD v4 |
| 5 | g.45645577T>G | CA359707873 | HCN1 | c.457A>C (p.Met153Leu) | |
| 5 | g.45645577T= | CA1543790787 | HCN1 | c.457A= (p.Met153=) | |
| 5 | g.45645578C>A | CA359707874 | HCN1 | c.456G>T (p.Met152Ile) | |
| 5 | g.45645578C>G | CA359707875 | HCN1 | c.456G>C (p.Met152Ile) | |
| 5 | g.45645578C>T | CA359707876 | HCN1 | c.456G>A (p.Met152Ile) | COSMIC |
| 5 | g.45645579A>C | CA359707877 | HCN1 | c.455T>G (p.Met152Arg) | |
| 5 | g.45645579A>G | CA359707879 | HCN1 | c.455T>C (p.Met152Thr) | |
| 5 | g.45645579A>T | CA359707878 | HCN1 | c.455T>A (p.Met152Lys) | |
| 5 | g.45645580T>A | CA359707880 | HCN1 | c.454A>T (p.Met152Leu) | |
| 5 | g.45645580T>C | CA359707881 | HCN1 | c.454A>G (p.Met152Val) | gnomAD v4 |
| 5 | g.45645580T>G | CA359707882 | HCN1 | c.454A>C (p.Met152Leu) | |
| 5 | g.45645581T>A | CA444401549 | HCN1 | c.453A>T (p.Ile151=) | |
| 5 | g.45645581T>C | CA359707883 | HCN1 | c.453A>G (p.Ile151Met) | |
| 5 | g.45645581T>G | CA3259437 | HCN1 | c.453A>C (p.Ile151=) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 5 | g.45645581T= | CA1543790789 | HCN1 | c.453A= (p.Ile151=) | |
| 5 | g.45645582A= | CA1543790794 | HCN1 | c.452T= (p.Ile151=) | |
| 5 | g.45645582A>C | CA359707886 | HCN1 | c.452T>G (p.Ile151Arg) | gnomAD v4 |
| 5 | g.45645582A>G | CA359707885 | HCN1 | c.452T>C (p.Ile151Thr) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.45645582A>T | CA359707884 | HCN1 | c.452T>A (p.Ile151Lys) | |
| 5 | g.45645583T>A | CA359707887 | HCN1 | c.451A>T (p.Ile151Leu) | dbSNP |
| 5 | g.45645583T>C | CA118324615 | HCN1 | c.451A>G (p.Ile151Val) | ClinVar dbSNP |
| 5 | g.45645583T>G | CA359707888 | HCN1 | c.451A>C (p.Ile151Leu) | |
| 5 | g.45645583T= | CA1543790798 | HCN1 | c.451A= (p.Ile151=) | |
| 5 | g.45645584A>C | CA444401555 | HCN1 | c.450T>G (p.Leu150=) | |
| 5 | g.45645584A>G | CA444401557 | HCN1 | c.450T>C (p.Leu150=) | gnomAD v4 |
| 5 | g.45645584A>T | CA444401556 | HCN1 | c.450T>A (p.Leu150=) | |
| 5 | g.45645585A= | CA1543790803 | HCN1 | c.449T= (p.Leu150=) | |
| 5 | g.45645585A>C | CA359707889 | HCN1 | c.449T>G (p.Leu150Arg) | |
| 5 | g.45645585A>G | CA359707890 | HCN1 | c.449T>C (p.Leu150Pro) | dbSNP gnomAD v2 gnomAD v4 |
| 5 | g.45645585A>T | CA359707891 | HCN1 | c.449T>A (p.Leu150His) | |
| 5 | g.45645586G>A | CA359707894 | HCN1 | c.448C>T (p.Leu150Phe) | |
| 5 | g.45645586G>C | CA359707892 | HCN1 | c.448C>G (p.Leu150Val) | |
| 5 | g.45645586G>T | CA359707893 | HCN1 | c.448C>A (p.Leu150Ile) | |
| 5 | g.45645587C>A | CA359707895 | HCN1 | c.447G>T (p.Met149Ile) | |
| 5 | g.45645587C= | CA1543790806 | HCN1 | c.447G= (p.Met149=) | |
| 5 | g.45645587C>G | CA359707896 | HCN1 | c.447G>C (p.Met149Ile) | |
| 5 | g.45645587C>T | CA359707897 | HCN1 | c.447G>A (p.Met149Ile) | dbSNP gnomAD v4 |
| 5 | g.45645588A= | CA1543790810 | HCN1 | c.446T= (p.Met149=) | |
| 5 | g.45645588A>C | CA359707898 | HCN1 | c.446T>G (p.Met149Arg) | dbSNP |
| 5 | g.45645588A>G | CA359707899 | HCN1 | c.446T>C (p.Met149Thr) | |
| 5 | g.45645588A>T | CA359707900 | HCN1 | c.446T>A (p.Met149Lys) |