Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.73323003G>A | CA491478112 | HCN4 | c.3090C>T (p.His1030=) c.1872C>T (p.His624=) | dbSNP gnomAD v2 gnomAD v4 |
15 | g.73323003G>C | CA393086237 | HCN4 | c.3090C>G (p.His1030Gln) c.1872C>G (p.His624Gln) | |
15 | g.73323003G= | CA2187187202 | HCN4 | c.3090C= (p.His1030=) c.1872C= (p.His624=) | |
15 | g.73323003G>T | CA393086238 | HCN4 | c.3090C>A (p.His1030Gln) c.1872C>A (p.His624Gln) | gnomAD v4 |
15 | g.73323004T>A | CA393086241 | HCN4 | c.3089A>T (p.His1030Leu) c.1871A>T (p.His624Leu) | |
15 | g.73323004T>C | CA393086240 | HCN4 | c.3089A>G (p.His1030Arg) c.1871A>G (p.His624Arg) | |
15 | g.73323004T>G | CA393086239 | HCN4 | c.3089A>C (p.His1030Pro) c.1871A>C (p.His624Pro) | |
15 | g.73323005G>A | CA393086244 | HCN4 | c.3088C>T (p.His1030Tyr) c.1870C>T (p.His624Tyr) | |
15 | g.73323005G>C | CA393086242 | HCN4 | c.3088C>G (p.His1030Asp) c.1870C>G (p.His624Asp) | |
15 | g.73323005G>T | CA393086243 | HCN4 | c.3088C>A (p.His1030Asn) c.1870C>A (p.His624Asn) | gnomAD v4 |
15 | g.73323006G>A | CA491478116 | HCN4 | c.3087C>T (p.Gly1029=) c.1869C>T (p.Gly623=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
15 | g.73323006G>C | CA491478118 | HCN4 | c.3087C>G (p.Gly1029=) c.1869C>G (p.Gly623=) | ClinVar dbSNP |
15 | g.73323006G= | CA2187187204 | HCN4 | c.3087C= (p.Gly1029=) c.1869C= (p.Gly623=) | |
15 | g.73323006G>T | CA491478120 | HCN4 | c.3087C>A (p.Gly1029=) c.1869C>A (p.Gly623=) | gnomAD v4 |
15 | g.73323007C>A | CA393086245 | HCN4 | c.3086G>T (p.Gly1029Val) c.1868G>T (p.Gly623Val) | gnomAD v4 |
15 | g.73323007C>G | CA393086246 | HCN4 | c.3086G>C (p.Gly1029Ala) c.1868G>C (p.Gly623Ala) | |
15 | g.73323007C>T | CA393086247 | HCN4 | c.3086G>A (p.Gly1029Asp) c.1868G>A (p.Gly623Asp) | gnomAD v4 |
15 | g.73323008C>A | CA393086250 | HCN4 | c.3085G>T (p.Gly1029Cys) c.1867G>T (p.Gly623Cys) | gnomAD v4 |
15 | g.73323008C>G | CA393086249 | HCN4 | c.3085G>C (p.Gly1029Arg) c.1867G>C (p.Gly623Arg) | |
15 | g.73323008C>T | CA393086248 | HCN4 | c.3085G>A (p.Gly1029Ser) c.1867G>A (p.Gly623Ser) | gnomAD v4 |
15 | g.73323009A>C | CA491478121 | HCN4 | c.3084T>G (p.Pro1028=) c.1866T>G (p.Pro622=) | |
15 | g.73323009A>G | CA491478122 | HCN4 | c.3084T>C (p.Pro1028=) c.1866T>C (p.Pro622=) | |
15 | g.73323009A>T | CA491478123 | HCN4 | c.3084T>A (p.Pro1028=) c.1866T>A (p.Pro622=) | |
15 | g.73323010G>A | CA393086251 | HCN4 | c.3083C>T (p.Pro1028Leu) c.1865C>T (p.Pro622Leu) | gnomAD v4 |
15 | g.73323010G>C | CA393086252 | HCN4 | c.3083C>G (p.Pro1028Arg) c.1865C>G (p.Pro622Arg) | ClinVar dbSNP gnomAD v4 |
15 | g.73323010G= | CA2187187206 | HCN4 | c.3083C= (p.Pro1028=) c.1865C= (p.Pro622=) | |
15 | g.73323010G>T | CA393086253 | HCN4 | c.3083C>A (p.Pro1028His) c.1865C>A (p.Pro622His) | gnomAD v4 |
15 | g.73323015dup | CA2575783828 | HCN4 | c.3083dup (p.Gly1029TrpfsTer?) c.1865dup (p.Gly623TrpfsTer?) | gnomAD v4 |
15 | g.73323015del | CA645586807 | HCN4 | c.3083del (p.Pro1028LeufsTer?) c.1865del (p.Pro622LeufsTer?) | gnomAD v4 COSMIC |
15 | g.73323011G>A | CA393086254 | HCN4 | c.3082C>T (p.Pro1028Ser) c.1864C>T (p.Pro622Ser) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
15 | g.73323011G>C | CA393086255 | HCN4 | c.3082C>G (p.Pro1028Ala) c.1864C>G (p.Pro622Ala) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
15 | g.73323011G= | CA2187187210 | HCN4 | c.3082C= (p.Pro1028=) c.1864C= (p.Pro622=) | |
15 | g.73323011G>T | CA393086256 | HCN4 | c.3082C>A (p.Pro1028Thr) c.1864C>A (p.Pro622Thr) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323012G>A | CA491478124 | HCN4 | c.3081C>T (p.Pro1027=) c.1863C>T (p.Pro621=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323012G>C | CA491478125 | HCN4 | c.3081C>G (p.Pro1027=) c.1863C>G (p.Pro621=) | |
15 | g.73323012G= | CA2187187214 | HCN4 | c.3081C= (p.Pro1027=) c.1863C= (p.Pro621=) | |
15 | g.73323012G>T | CA491478126 | HCN4 | c.3081C>A (p.Pro1027=) c.1863C>A (p.Pro621=) | gnomAD v4 |
15 | g.73323013G>A | CA7648886 | HCN4 | c.3080C>T (p.Pro1027Leu) c.1862C>T (p.Pro621Leu) | dbSNP ExAC gnomAD v2 |
15 | g.73323013G>C | CA393086257 | HCN4 | c.3080C>G (p.Pro1027Arg) c.1862C>G (p.Pro621Arg) | |
15 | g.73323013G= | CA2187187223 | HCN4 | c.3080C= (p.Pro1027=) c.1862C= (p.Pro621=) | |
15 | g.73323013G>T | CA272663752 | HCN4 | c.3080C>A (p.Pro1027His) c.1862C>A (p.Pro621His) | dbSNP gnomAD v4 |
15 | g.73323014G>A | CA393086258 | HCN4 | c.3079C>T (p.Pro1027Ser) c.1861C>T (p.Pro621Ser) | ClinVar |
15 | g.73323014G>C | CA393086259 | HCN4 | c.3079C>G (p.Pro1027Ala) c.1861C>G (p.Pro621Ala) | gnomAD v4 |
15 | g.73323014G= | CA2187187225 | HCN4 | c.3079C= (p.Pro1027=) c.1861C= (p.Pro621=) | |
15 | g.73323014G>T | CA393086260 | HCN4 | c.3079C>A (p.Pro1027Thr) c.1861C>A (p.Pro621Thr) | dbSNP gnomAD v4 |
15 | g.73323015G>A | CA7648887 | HCN4 | c.3078C>T (p.Ser1026=) c.1860C>T (p.Ser620=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323015G>C | CA393086261 | HCN4 | c.3078C>G (p.Ser1026Arg) c.1860C>G (p.Ser620Arg) | gnomAD v4 |
15 | g.73323015G= | CA2187187229 | HCN4 | c.3078C= (p.Ser1026=) c.1860C= (p.Ser620=) | |
15 | g.73323015G>T | CA393086262 | HCN4 | c.3078C>A (p.Ser1026Arg) c.1860C>A (p.Ser620Arg) | gnomAD v4 |
15 | g.73323016C>A | CA393086263 | HCN4 | c.3077G>T (p.Ser1026Ile) c.1859G>T (p.Ser620Ile) | gnomAD v4 |