Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
5 | g.45645487C>A | CA359707669 | HCN1 | c.547G>T (p.Asp183Tyr) | |
5 | g.45645487C>G | CA359707670 | HCN1 | c.547G>C (p.Asp183His) | COSMIC |
5 | g.45645487C>T | CA359707671 | HCN1 | c.547G>A (p.Asp183Asn) | COSMIC |
5 | g.45645488T>A | CA444401393 | HCN1 | c.546A>T (p.Ser182=) | |
5 | g.45645488T>C | CA3259433 | HCN1 | c.546A>G (p.Ser182=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.45645488T>G | CA444401395 | HCN1 | c.546A>C (p.Ser182=) | |
5 | g.45645488T= | CA1543790662 | HCN1 | c.546A= (p.Ser182=) | |
5 | g.45645489G>A | CA359707674 | HCN1 | c.545C>T (p.Ser182Leu) | |
5 | g.45645489G>C | CA359707673 | HCN1 | c.545C>G (p.Ser182Ter) | |
5 | g.45645489G>T | CA359707672 | HCN1 | c.545C>A (p.Ser182Ter) | |
5 | g.45645490A>C | CA359707675 | HCN1 | c.544T>G (p.Ser182Ala) | |
5 | g.45645490A>G | CA359707676 | HCN1 | c.544T>C (p.Ser182Pro) | |
5 | g.45645490A>T | CA359707677 | HCN1 | c.544T>A (p.Ser182Thr) | |
5 | g.45645491T>A | CA444401398 | HCN1 | c.543A>T (p.Ala181=) | dbSNP gnomAD v3 gnomAD v4 |
5 | g.45645491T>C | CA3259434 | HCN1 | c.543A>G (p.Ala181=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
5 | g.45645491T>G | CA444401399 | HCN1 | c.543A>C (p.Ala181=) | |
5 | g.45645491T= | CA1543790667 | HCN1 | c.543A= (p.Ala181=) | |
5 | g.45645492G>A | CA359707678 | HCN1 | c.542C>T (p.Ala181Val) | |
5 | g.45645492G>C | CA359707679 | HCN1 | c.542C>G (p.Ala181Gly) | |
5 | g.45645492G>T | CA359707680 | HCN1 | c.542C>A (p.Ala181Glu) | |
5 | g.45645493C>A | CA359707681 | HCN1 | c.541G>T (p.Ala181Ser) | dbSNP gnomAD v4 COSMIC |
5 | g.45645493C= | CA1543790672 | HCN1 | c.541G= (p.Ala181=) | |
5 | g.45645493C>G | CA359707682 | HCN1 | c.541G>C (p.Ala181Pro) | |
5 | g.45645493C>T | CA359707683 | HCN1 | c.541G>A (p.Ala181Thr) | |
5 | g.45645494C>A | CA444401401 | HCN1 | c.540G>T (p.Val180=) | |
5 | g.45645494C>G | CA444401403 | HCN1 | c.540G>C (p.Val180=) | |
5 | g.45645494C>T | CA444401405 | HCN1 | c.540G>A (p.Val180=) | gnomAD v4 COSMIC |
5 | g.45645495A>C | CA359707684 | HCN1 | c.539T>G (p.Val180Gly) | |
5 | g.45645495A>G | CA359707685 | HCN1 | c.539T>C (p.Val180Ala) | |
5 | g.45645495A>T | CA359707686 | HCN1 | c.539T>A (p.Val180Glu) | |
5 | g.45645496C>A | CA359707688 | HCN1 | c.538G>T (p.Val180Leu) | dbSNP |
5 | g.45645496C>G | CA359707689 | HCN1 | c.538G>C (p.Val180Leu) | |
5 | g.45645496C>T | CA359707687 | HCN1 | c.538G>A (p.Val180Met) | |
5 | g.45645497A= | CA1543790679 | HCN1 | c.537T= (p.Asn179=) | |
5 | g.45645497A>C | CA359707690 | HCN1 | c.537T>G (p.Asn179Lys) | |
5 | g.45645497A>G | CA118324612 | HCN1 | c.537T>C (p.Asn179=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.45645497A>T | CA359707691 | HCN1 | c.537T>A (p.Asn179Lys) | |
5 | g.45645498T>A | CA359707692 | HCN1 | c.536A>T (p.Asn179Ile) | |
5 | g.45645498T>C | CA359707693 | HCN1 | c.536A>G (p.Asn179Ser) | dbSNP |
5 | g.45645498T>G | CA359707694 | HCN1 | c.536A>C (p.Asn179Thr) | |
5 | g.45645498T= | CA1543790694 | HCN1 | c.536A= (p.Asn179=) | |
5 | g.45645499T>A | CA359707695 | HCN1 | c.535A>T (p.Asn179Tyr) | ClinVar |
5 | g.45645499T>C | CA359707696 | HCN1 | c.535A>G (p.Asn179Asp) | |
5 | g.45645499T>G | CA359707697 | HCN1 | c.535A>C (p.Asn179His) | |
5 | g.45645500G>A | CA444401412 | HCN1 | c.534C>T (p.Phe178=) | |
5 | g.45645500G>C | CA359707698 | HCN1 | c.534C>G (p.Phe178Leu) | |
5 | g.45645500G>T | CA359707699 | HCN1 | c.534C>A (p.Phe178Leu) | |
5 | g.45645501A>C | CA359707700 | HCN1 | c.533T>G (p.Phe178Cys) | |
5 | g.45645501A>G | CA359707702 | HCN1 | c.533T>C (p.Phe178Ser) | |
5 | g.45645501A>T | CA359707701 | HCN1 | c.533T>A (p.Phe178Tyr) |