Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.73323059dup | CA7648896 | HCN4 | c.3040dup (p.Ala1014GlyfsTer?) c.1822dup (p.Ala608GlyfsTer?) | dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73323058_73323059dup | CA2804714151 | HCN4 | c.3039_3040dup (p.Ala1014GlyfsTer5) c.1821_1822dup (p.Ala608GlyfsTer5) | |
15 | g.73323059del | CA645586808 | HCN4 | c.3040del (p.Ala1014LeufsTer4) c.1822del (p.Ala608LeufsTer4) | gnomAD v4 COSMIC |
15 | g.73323059C>A | CA7648898 | HCN4 | c.3034G>T (p.Gly1012Trp) c.1816G>T (p.Gly606Trp) | dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73323059C= | CA2187187364 | HCN4 | c.3034G= (p.Gly1012=) c.1816G= (p.Gly606=) | |
15 | g.73323059C>G | CA393086382 | HCN4 | c.3034G>C (p.Gly1012Arg) c.1816G>C (p.Gly606Arg) | dbSNP gnomAD v4 |
15 | g.73323059C>T | CA7648899 | HCN4 | c.3034G>A (p.Gly1012Arg) c.1816G>A (p.Gly606Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73323060A= | CA2187187372 | HCN4 | c.3033T= (p.Ser1011=) c.1815T= (p.Ser605=) | |
15 | g.73323060A>C | CA199745 | HCN4 | c.3033T>G (p.Ser1011=) c.1815T>G (p.Ser605=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323060A>G | CA491478417 | HCN4 | c.3033T>C (p.Ser1011=) c.1815T>C (p.Ser605=) | gnomAD v4 |
15 | g.73323060A>T | CA491478418 | HCN4 | c.3033T>A (p.Ser1011=) c.1815T>A (p.Ser605=) | |
15 | g.73323061G>A | CA393086385 | HCN4 | c.3032C>T (p.Ser1011Phe) c.1814C>T (p.Ser605Phe) | gnomAD v4 |
15 | g.73323061G>C | CA393086387 | HCN4 | c.3032C>G (p.Ser1011Cys) c.1814C>G (p.Ser605Cys) | |
15 | g.73323061G>T | CA393086389 | HCN4 | c.3032C>A (p.Ser1011Tyr) c.1814C>A (p.Ser605Tyr) | gnomAD v4 |
15 | g.73323062A= | CA2187187378 | HCN4 | c.3031T= (p.Ser1011=) c.1813T= (p.Ser605=) | |
15 | g.73323062A>C | CA393086391 | HCN4 | c.3031T>G (p.Ser1011Ala) c.1813T>G (p.Ser605Ala) | gnomAD v4 |
15 | g.73323062A>G | CA16607866 | HCN4 | c.3031T>C (p.Ser1011Pro) c.1813T>C (p.Ser605Pro) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
15 | g.73323062A>T | CA393086393 | HCN4 | c.3031T>A (p.Ser1011Thr) c.1813T>A (p.Ser605Thr) | |
15 | g.73323063G>A | CA7648900 | HCN4 | c.3030C>T (p.Ala1010=) c.1812C>T (p.Ala604=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323063G>C | CA491478426 | HCN4 | c.3030C>G (p.Ala1010=) c.1812C>G (p.Ala604=) | |
15 | g.73323063G= | CA2187187381 | HCN4 | c.3030C= (p.Ala1010=) c.1812C= (p.Ala604=) | |
15 | g.73323063G>T | CA491478425 | HCN4 | c.3030C>A (p.Ala1010=) c.1812C>A (p.Ala604=) | gnomAD v4 |
15 | g.73323064G>A | CA393086397 | HCN4 | c.3029C>T (p.Ala1010Val) c.1811C>T (p.Ala604Val) | gnomAD v4 |
15 | g.73323064G>C | CA393086399 | HCN4 | c.3029C>G (p.Ala1010Gly) c.1811C>G (p.Ala604Gly) | gnomAD v4 |
15 | g.73323064G= | CA2187187384 | HCN4 | c.3029C= (p.Ala1010=) c.1811C= (p.Ala604=) | |
15 | g.73323064G>T | CA393086396 | HCN4 | c.3029C>A (p.Ala1010Asp) c.1811C>A (p.Ala604Asp) | gnomAD v4 |
15 | g.73323065C>A | CA393086402 | HCN4 | c.3028G>T (p.Ala1010Ser) c.1810G>T (p.Ala604Ser) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323065C= | CA2187187391 | HCN4 | c.3028G= (p.Ala1010=) c.1810G= (p.Ala604=) | |
15 | g.73323065C>G | CA393086404 | HCN4 | c.3028G>C (p.Ala1010Pro) c.1810G>C (p.Ala604Pro) | |
15 | g.73323065C>T | CA7648901 | HCN4 | c.3028G>A (p.Ala1010Thr) c.1810G>A (p.Ala604Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73323068dup | CA272663932 | HCN4 | c.3028dup (p.Ala1010GlyfsTer?) c.1810dup (p.Ala604GlyfsTer?) | dbSNP gnomAD v4 |
15 | g.73323068del | CA2629370545 | HCN4 | c.3028del (p.Ala1010ProfsTer8) c.1810del (p.Ala604ProfsTer8) | gnomAD v4 |
15 | g.73323066C>A | CA491478437 | HCN4 | c.3027G>T (p.Gly1009=) c.1809G>T (p.Gly603=) | gnomAD v4 |
15 | g.73323066C>G | CA491478438 | HCN4 | c.3027G>C (p.Gly1009=) c.1809G>C (p.Gly603=) | |
15 | g.73323066C>T | CA491478440 | HCN4 | c.3027G>A (p.Gly1009=) c.1809G>A (p.Gly603=) | |
15 | g.73323067C>A | CA393086406 | HCN4 | c.3026G>T (p.Gly1009Val) c.1808G>T (p.Gly603Val) | |
15 | g.73323067C= | CA2187187397 | HCN4 | c.3026G= (p.Gly1009=) c.1808G= (p.Gly603=) | |
15 | g.73323067C>G | CA393086407 | HCN4 | c.3026G>C (p.Gly1009Ala) c.1808G>C (p.Gly603Ala) | |
15 | g.73323067C>T | CA7648902 | HCN4 | c.3026G>A (p.Gly1009Glu) c.1808G>A (p.Gly603Glu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73323068C>A | CA393086410 | HCN4 | c.3025G>T (p.Gly1009Trp) c.1807G>T (p.Gly603Trp) | |
15 | g.73323068C>G | CA393086411 | HCN4 | c.3025G>C (p.Gly1009Arg) c.1807G>C (p.Gly603Arg) | gnomAD v4 |
15 | g.73323068C>T | CA393086413 | HCN4 | c.3025G>A (p.Gly1009Arg) c.1807G>A (p.Gly603Arg) | gnomAD v4 |
15 | g.73323069T>A | CA491478447 | HCN4 | c.3024A>T (p.Ala1008=) c.1806A>T (p.Ala602=) | |
15 | g.73323069T>C | CA491478448 | HCN4 | c.3024A>G (p.Ala1008=) c.1806A>G (p.Ala602=) | gnomAD v4 |
15 | g.73323069T>G | CA491478449 | HCN4 | c.3024A>C (p.Ala1008=) c.1806A>C (p.Ala602=) | |
15 | g.73323070G>A | CA393086415 | HCN4 | c.3023C>T (p.Ala1008Val) c.1805C>T (p.Ala602Val) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323070G>C | CA393086417 | HCN4 | c.3023C>G (p.Ala1008Gly) c.1805C>G (p.Ala602Gly) | |
15 | g.73323070G= | CA2187187400 | HCN4 | c.3023C= (p.Ala1008=) c.1805C= (p.Ala602=) | |
15 | g.73323070G>T | CA393086419 | HCN4 | c.3023C>A (p.Ala1008Glu) c.1805C>A (p.Ala602Glu) | gnomAD v4 |
15 | g.73323071C>A | CA393086424 | HCN4 | c.3022G>T (p.Ala1008Ser) c.1804G>T (p.Ala602Ser) | ClinVar dbSNP gnomAD v4 |