| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 5 | g.45461944T>A | CA16604906 | HCN1 | c.913A>T (p.Met305Leu) n.76A>T | ClinVar dbSNP |
| 5 | g.45461944T>C | CA359704971 | HCN1 | c.913A>G (p.Met305Val) n.76A>G | |
| 5 | g.45461944T>G | CA359704972 | HCN1 | c.913A>C (p.Met305Leu) n.76A>C | |
| 5 | g.45461944T= | CA1543688341 | HCN1 | c.913A= (p.Met305=) n.76A= | |
| 5 | g.45461945C>A | CA359704973 | HCN1 | c.912G>T (p.Met304Ile) n.75G>T | |
| 5 | g.45461945C>G | CA359704974 | HCN1 | c.912G>C (p.Met304Ile) n.75G>C | |
| 5 | g.45461945C>T | CA359704975 | HCN1 | c.912G>A (p.Met304Ile) n.75G>A | |
| 5 | g.45461946A>C | CA359704976 | HCN1 | c.911T>G (p.Met304Arg) n.74T>G | |
| 5 | g.45461946A>G | CA359704977 | HCN1 | c.911T>C (p.Met304Thr) n.74T>C | |
| 5 | g.45461946A>T | CA359704978 | HCN1 | c.911T>A (p.Met304Lys) n.74T>A | |
| 5 | g.45461947T>A | CA359704979 | HCN1 | c.910A>T (p.Met304Leu) n.73A>T | |
| 5 | g.45461947T>C | CA359704980 | HCN1 | c.910A>G (p.Met304Val) n.73A>G | |
| 5 | g.45461947T>G | CA359704981 | HCN1 | c.910A>C (p.Met304Leu) n.73A>C | |
| 5 | g.45461948G>A | CA444258191 | HCN1 | c.909C>T (p.Gly303=) n.72C>T | |
| 5 | g.45461948G>C | CA444258193 | HCN1 | c.909C>G (p.Gly303=) n.72C>G | |
| 5 | g.45461948G= | CA1543688347 | HCN1 | c.909C= (p.Gly303=) n.72C= | |
| 5 | g.45461948G>T | CA3259392 | HCN1 | c.909C>A (p.Gly303=) n.72C>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 5 | g.45461949C>A | CA359704984 | HCN1 | c.908G>T (p.Gly303Val) n.71G>T | ClinVar |
| 5 | g.45461949C>G | CA359704982 | HCN1 | c.908G>C (p.Gly303Ala) n.71G>C | |
| 5 | g.45461949C>T | CA359704983 | HCN1 | c.908G>A (p.Gly303Asp) n.71G>A | |
| 5 | g.45461950C>A | CA359704985 | HCN1 | c.907G>T (p.Gly303Cys) n.70G>T | |
| 5 | g.45461950C= | CA1543688351 | HCN1 | c.907G= (p.Gly303=) n.70G= | |
| 5 | g.45461950C>G | CA359704986 | HCN1 | c.907G>C (p.Gly303Arg) n.70G>C | |
| 5 | g.45461950C>T | CA359704987 | HCN1 | c.907G>A (p.Gly303Ser) n.70G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.45461951G>A | CA118303545 | HCN1 | c.906C>T (p.Ile302=) n.69C>T | dbSNP gnomAD v4 COSMIC |
| 5 | g.45461951G>C | CA359704988 | HCN1 | c.906C>G (p.Ile302Met) n.69C>G | |
| 5 | g.45461951G= | CA1543688357 | HCN1 | c.906C= (p.Ile302=) n.69C= | |
| 5 | g.45461951G>T | CA444258199 | HCN1 | c.906C>A (p.Ile302=) n.69C>A | |
| 5 | g.45461952A>C | CA359704989 | HCN1 | c.905T>G (p.Ile302Ser) n.68T>G | |
| 5 | g.45461952A>G | CA359704991 | HCN1 | c.905T>C (p.Ile302Thr) n.68T>C | |
| 5 | g.45461952A>T | CA359704990 | HCN1 | c.905T>A (p.Ile302Asn) n.68T>A | |
| 5 | g.45461953T>A | CA359704992 | HCN1 | c.904A>T (p.Ile302Phe) n.67A>T | COSMIC |
| 5 | g.45461953T>C | CA359704993 | HCN1 | c.904A>G (p.Ile302Val) n.67A>G | |
| 5 | g.45461953T>G | CA359704994 | HCN1 | c.904A>C (p.Ile302Leu) n.67A>C | gnomAD v4 |
| 5 | g.45461954G>A | CA3259393 | HCN1 | c.903C>T (p.Leu301=) n.66C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 5 | g.45461954G>C | CA444258207 | HCN1 | c.903C>G (p.Leu301=) n.66C>G | |
| 5 | g.45461954G= | CA1543688364 | HCN1 | c.903C= (p.Leu301=) n.66C= | |
| 5 | g.45461954G>T | CA444258205 | HCN1 | c.903C>A (p.Leu301=) n.66C>A | |
| 5 | g.45461955A>C | CA359704995 | HCN1 | c.902T>G (p.Leu301Arg) n.65T>G | |
| 5 | g.45461955A>G | CA359704997 | HCN1 | c.902T>C (p.Leu301Pro) n.65T>C | |
| 5 | g.45461955A>T | CA359704996 | HCN1 | c.902T>A (p.Leu301His) n.65T>A | |
| 5 | g.45461956G>A | CA359704998 | HCN1 | c.901C>T (p.Leu301Phe) n.64C>T | COSMIC |
| 5 | g.45461956G>C | CA359704999 | HCN1 | c.901C>G (p.Leu301Val) n.64C>G | |
| 5 | g.45461956G>T | CA359705000 | HCN1 | c.901C>A (p.Leu301Ile) n.64C>A | |
| 5 | g.45461957A>C | CA359705001 | HCN1 | c.900T>G (p.Asn300Lys) n.63T>G | |
| 5 | g.45461957A>G | CA444258213 | HCN1 | c.900T>C (p.Asn300=) n.63T>C | gnomAD v3 gnomAD v4 |
| 5 | g.45461957A>T | CA359705002 | HCN1 | c.900T>A (p.Asn300Lys) n.63T>A | |
| 5 | g.45461958T>A | CA359705003 | HCN1 | c.899A>T (p.Asn300Ile) n.62A>T | ClinVar |
| 5 | g.45461958T>C | CA359705004 | HCN1 | c.899A>G (p.Asn300Ser) n.62A>G | |
| 5 | g.45461958T>G | CA359705005 | HCN1 | c.899A>C (p.Asn300Thr) n.62A>C |