Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
5 | g.45645220A= | CA1543790275 | HCN1 | c.814T= (p.Ser272=) n.42T= | |
5 | g.45645220A>C | CA359707058 | HCN1 | c.814T>G (p.Ser272Ala) n.42T>G | |
5 | g.45645220A>G | CA163273 | HCN1 | c.814T>C (p.Ser272Pro) n.42T>C | ClinVar dbSNP |
5 | g.45645220A>T | CA359707057 | HCN1 | c.814T>A (p.Ser272Thr) n.42T>A | |
5 | g.45645221A>C | CA444260289 | HCN1 | c.813T>G (p.Leu271=) n.41T>G | |
5 | g.45645221A>G | CA444260291 | HCN1 | c.813T>C (p.Leu271=) n.41T>C | |
5 | g.45645221A>T | CA444260292 | HCN1 | c.813T>A (p.Leu271=) n.41T>A | |
5 | g.45645222A>C | CA359707059 | HCN1 | c.812T>G (p.Leu271Arg) n.40T>G | |
5 | g.45645222A>G | CA359707060 | HCN1 | c.812T>C (p.Leu271Pro) n.40T>C | |
5 | g.45645222A>T | CA359707061 | HCN1 | c.812T>A (p.Leu271His) n.40T>A | |
5 | g.45645223G>A | CA359707062 | HCN1 | c.811C>T (p.Leu271Phe) n.39C>T | |
5 | g.45645223G>C | CA359707063 | HCN1 | c.811C>G (p.Leu271Val) n.39C>G | |
5 | g.45645223G>T | CA359707064 | HCN1 | c.811C>A (p.Leu271Ile) n.39C>A | |
5 | g.45645224T>A | CA444260301 | HCN1 | c.810A>T (p.Arg270=) n.38A>T | |
5 | g.45645224T>C | CA444260303 | HCN1 | c.810A>G (p.Arg270=) n.38A>G | gnomAD v4 |
5 | g.45645224T>G | CA444260304 | HCN1 | c.810A>C (p.Arg270=) n.38A>C | |
5 | g.45645225C>A | CA359707065 | HCN1 | c.809G>T (p.Arg270Leu) n.37G>T | |
5 | g.45645225C>G | CA359707067 | HCN1 | c.809G>C (p.Arg270Pro) n.37G>C | |
5 | g.45645225C>T | CA359707066 | HCN1 | c.809G>A (p.Arg270Gln) n.37G>A | ClinVar dbSNP gnomAD v4 COSMIC |
5 | g.45645226G>A | CA3259415 | HCN1 | c.808C>T (p.Arg270Ter) n.36C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
5 | g.45645226G>C | CA359707068 | HCN1 | c.808C>G (p.Arg270Gly) n.36C>G | |
5 | g.45645226G= | CA1543790288 | HCN1 | c.808C= (p.Arg270=) n.36C= | |
5 | g.45645226G>T | CA444260310 | HCN1 | c.808C>A (p.Arg270=) n.36C>A | |
5 | g.45645227T>A | CA359707069 | HCN1 | c.807A>T (p.Leu269Phe) n.35A>T | |
5 | g.45645227T>C | CA444260314 | HCN1 | c.807A>G (p.Leu269=) n.35A>G | |
5 | g.45645227T>G | CA359707070 | HCN1 | c.807A>C (p.Leu269Phe) n.35A>C | |
5 | g.45645228A>C | CA359707073 | HCN1 | c.806T>G (p.Leu269Ter) n.34T>G | |
5 | g.45645228A>G | CA359707072 | HCN1 | c.806T>C (p.Leu269Ser) n.34T>C | |
5 | g.45645228A>T | CA359707071 | HCN1 | c.806T>A (p.Leu269Ter) n.34T>A | |
5 | g.45645229A>C | CA359707074 | HCN1 | c.805T>G (p.Leu269Val) n.33T>G | COSMIC |
5 | g.45645229A>G | CA444260321 | HCN1 | c.805T>C (p.Leu269=) n.33T>C | |
5 | g.45645229A>T | CA359707075 | HCN1 | c.805T>A (p.Leu269Ile) n.33T>A | |
5 | g.45645230T>A | CA359707076 | HCN1 | c.804A>T (p.Leu268Phe) n.32A>T | |
5 | g.45645230T>C | CA444260324 | HCN1 | c.804A>G (p.Leu268=) n.32A>G | dbSNP |
5 | g.45645230T>G | CA359707077 | HCN1 | c.804A>C (p.Leu268Phe) n.32A>C | |
5 | g.45645230T= | CA1543790295 | HCN1 | c.804A= (p.Leu268=) n.32A= | |
5 | g.45645231A>C | CA359707078 | HCN1 | c.803T>G (p.Leu268Ter) n.31T>G | |
5 | g.45645231A>G | CA359707079 | HCN1 | c.803T>C (p.Leu268Ser) n.31T>C | COSMIC |
5 | g.45645231A>T | CA359707080 | HCN1 | c.803T>A (p.Leu268Ter) n.31T>A | |
5 | g.45645233del | CA2578305117 | HCN1 | c.803del (p.Leu268TyrfsTer7) n.31del | |
5 | g.45645232A>C | CA359707081 | HCN1 | c.802T>G (p.Leu268Val) n.30T>G | |
5 | g.45645232A>G | CA444401523 | HCN1 | c.802T>C (p.Leu268=) n.30T>C | |
5 | g.45645232A>T | CA359707082 | HCN1 | c.802T>A (p.Leu268Ile) n.30T>A | |
5 | g.45645233A>C | CA444401524 | HCN1 | c.801T>G (p.Arg267=) n.29T>G | |
5 | g.45645233A>G | CA444401525 | HCN1 | c.801T>C (p.Arg267=) n.29T>C | gnomAD v4 |
5 | g.45645233A>T | CA444401526 | HCN1 | c.801T>A (p.Arg267=) n.29T>A | |
5 | g.45645234C>A | CA359707083 | HCN1 | c.800G>T (p.Arg267Leu) n.28G>T | COSMIC |
5 | g.45645234C= | CA1543790299 | HCN1 | c.800G= (p.Arg267=) n.28G= | |
5 | g.45645234C>G | CA359707084 | HCN1 | c.800G>C (p.Arg267Pro) n.28G>C | dbSNP |
5 | g.45645234C>T | CA118324606 | HCN1 | c.800G>A (p.Arg267His) n.28G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |