Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.73325118C>A | CA491479082 | HCN4 | c.1815G>T (p.Thr605=) c.597G>T (p.Thr199=) | |
15 | g.73325118C= | CA2187190541 | HCN4 | c.1815G= (p.Thr605=) c.597G= (p.Thr199=) | |
15 | g.73325118C>G | CA491479083 | HCN4 | c.1815G>C (p.Thr605=) c.597G>C (p.Thr199=) | |
15 | g.73325118C>T | CA7649181 | HCN4 | c.1815G>A (p.Thr605=) c.597G>A (p.Thr199=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
15 | g.73325119G>A | CA272666402 | HCN4 | c.1814C>T (p.Thr605Met) c.596C>T (p.Thr199Met) | dbSNP gnomAD v3 gnomAD v4 COSMIC |
15 | g.73325119G>C | CA393090819 | HCN4 | c.1814C>G (p.Thr605Arg) c.596C>G (p.Thr199Arg) | |
15 | g.73325119G= | CA2187190550 | HCN4 | c.1814C= (p.Thr605=) c.596C= (p.Thr199=) | |
15 | g.73325119G>T | CA393090820 | HCN4 | c.1814C>A (p.Thr605Lys) c.596C>A (p.Thr199Lys) | COSMIC |
15 | g.73325120T>A | CA393090821 | HCN4 | c.1813A>T (p.Thr605Ser) c.595A>T (p.Thr199Ser) | |
15 | g.73325120T>C | CA393090822 | HCN4 | c.1813A>G (p.Thr605Ala) c.595A>G (p.Thr199Ala) | gnomAD v4 |
15 | g.73325120T>G | CA393090823 | HCN4 | c.1813A>C (p.Thr605Pro) c.595A>C (p.Thr199Pro) | |
15 | g.73325121C>A | CA491479084 | HCN4 | c.1812G>T (p.Val604=) c.594G>T (p.Val198=) | |
15 | g.73325121C= | CA2187190555 | HCN4 | c.1812G= (p.Val604=) c.594G= (p.Val198=) | |
15 | g.73325121C>G | CA491479085 | HCN4 | c.1812G>C (p.Val604=) c.594G>C (p.Val198=) | |
15 | g.73325121C>T | CA16607873 | HCN4 | c.1812G>A (p.Val604=) c.594G>A (p.Val198=) | ClinVar dbSNP gnomAD v4 |
15 | g.73325122A>C | CA393090825 | HCN4 | c.1811T>G (p.Val604Gly) c.593T>G (p.Val198Gly) | |
15 | g.73325122A>G | CA393090827 | HCN4 | c.1811T>C (p.Val604Ala) c.593T>C (p.Val198Ala) | |
15 | g.73325122A>T | CA393090829 | HCN4 | c.1811T>A (p.Val604Glu) c.593T>A (p.Val198Glu) | |
15 | g.73325123C>A | CA393090835 | HCN4 | c.1810G>T (p.Val604Leu) c.592G>T (p.Val198Leu) | |
15 | g.73325123C= | CA2187190558 | HCN4 | c.1810G= (p.Val604=) c.592G= (p.Val198=) | |
15 | g.73325123C>G | CA393090834 | HCN4 | c.1810G>C (p.Val604Leu) c.592G>C (p.Val198Leu) | |
15 | g.73325123C>T | CA393090831 | HCN4 | c.1810G>A (p.Val604Met) c.592G>A (p.Val198Met) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73325124G>A | CA7649182 | HCN4 | c.1809C>T (p.Phe603=) c.591C>T (p.Phe197=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73325124G>C | CA393090838 | HCN4 | c.1809C>G (p.Phe603Leu) c.591C>G (p.Phe197Leu) | gnomAD v4 |
15 | g.73325124G= | CA2187190565 | HCN4 | c.1809C= (p.Phe603=) c.591C= (p.Phe197=) | |
15 | g.73325124G>T | CA393090839 | HCN4 | c.1809C>A (p.Phe603Leu) c.591C>A (p.Phe197Leu) | ClinVar dbSNP |
15 | g.73325125A>C | CA393090842 | HCN4 | c.1808T>G (p.Phe603Cys) c.590T>G (p.Phe197Cys) | |
15 | g.73325125A>G | CA393090844 | HCN4 | c.1808T>C (p.Phe603Ser) c.590T>C (p.Phe197Ser) | |
15 | g.73325125A>T | CA393090846 | HCN4 | c.1808T>A (p.Phe603Tyr) c.590T>A (p.Phe197Tyr) | |
15 | g.73325126A= | CA2187190573 | HCN4 | c.1807T= (p.Phe603=) c.589T= (p.Phe197=) | |
15 | g.73325126A>C | CA393090848 | HCN4 | c.1807T>G (p.Phe603Val) c.589T>G (p.Phe197Val) | |
15 | g.73325126A>G | CA393090851 | HCN4 | c.1807T>C (p.Phe603Leu) c.589T>C (p.Phe197Leu) | dbSNP gnomAD v4 |
15 | g.73325126A>T | CA393090850 | HCN4 | c.1807T>A (p.Phe603Ile) c.589T>A (p.Phe197Ile) | gnomAD v4 |
15 | g.73325127G>A | CA491479086 | HCN4 | c.1806C>T (p.Asn602=) c.588C>T (p.Asn196=) | |
15 | g.73325127G>C | CA393090854 | HCN4 | c.1806C>G (p.Asn602Lys) c.588C>G (p.Asn196Lys) | |
15 | g.73325127G>T | CA393090855 | HCN4 | c.1806C>A (p.Asn602Lys) c.588C>A (p.Asn196Lys) | |
15 | g.73325128T>A | CA393090858 | HCN4 | c.1805A>T (p.Asn602Ile) c.587A>T (p.Asn196Ile) | |
15 | g.73325128T>C | CA393090860 | HCN4 | c.1805A>G (p.Asn602Ser) c.587A>G (p.Asn196Ser) | ClinVar gnomAD v4 |
15 | g.73325128T>G | CA393090861 | HCN4 | c.1805A>C (p.Asn602Thr) c.587A>C (p.Asn196Thr) | |
15 | g.73325129T>A | CA393090862 | HCN4 | c.1804A>T (p.Asn602Tyr) c.586A>T (p.Asn196Tyr) | |
15 | g.73325129T>C | CA393090865 | HCN4 | c.1804A>G (p.Asn602Asp) c.586A>G (p.Asn196Asp) | |
15 | g.73325129T>G | CA393090867 | HCN4 | c.1804A>C (p.Asn602His) c.586A>C (p.Asn196His) | |
15 | g.73325130G>A | CA491479087 | HCN4 | c.1803C>T (p.Pro601=) c.585C>T (p.Pro195=) | |
15 | g.73325130G>C | CA491479088 | HCN4 | c.1803C>G (p.Pro601=) c.585C>G (p.Pro195=) | |
15 | g.73325130G>T | CA491479089 | HCN4 | c.1803C>A (p.Pro601=) c.585C>A (p.Pro195=) | |
15 | g.73325131G>A | CA393090869 | HCN4 | c.1802C>T (p.Pro601Leu) c.584C>T (p.Pro195Leu) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73325131G>C | CA393090871 | HCN4 | c.1802C>G (p.Pro601Arg) c.584C>G (p.Pro195Arg) | |
15 | g.73325131G= | CA2187190576 | HCN4 | c.1802C= (p.Pro601=) c.584C= (p.Pro195=) | |
15 | g.73325131G>T | CA393090873 | HCN4 | c.1802C>A (p.Pro601His) c.584C>A (p.Pro195His) | |
15 | g.73325132G>A | CA393090879 | HCN4 | c.1801C>T (p.Pro601Ser) c.583C>T (p.Pro195Ser) | ClinVar |