Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.73322773T>A | CA7648846 | HCN4 | c.3320A>T (p.His1107Leu) c.2102A>T (p.His701Leu) | dbSNP ExAC gnomAD v2 |
15 | g.73322773T>C | CA393085632 | HCN4 | c.3320A>G (p.His1107Arg) c.2102A>G (p.His701Arg) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
15 | g.73322773T>G | CA393085630 | HCN4 | c.3320A>C (p.His1107Pro) c.2102A>C (p.His701Pro) | |
15 | g.73322773T= | CA2187186681 | HCN4 | c.3320A= (p.His1107=) c.2102A= (p.His701=) | |
15 | g.73322774G>A | CA393085637 | HCN4 | c.3319C>T (p.His1107Tyr) c.2101C>T (p.His701Tyr) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73322774G>C | CA393085639 | HCN4 | c.3319C>G (p.His1107Asp) c.2101C>G (p.His701Asp) | |
15 | g.73322774G= | CA2187186687 | HCN4 | c.3319C= (p.His1107=) c.2101C= (p.His701=) | |
15 | g.73322774G>T | CA393085641 | HCN4 | c.3319C>A (p.His1107Asn) c.2101C>A (p.His701Asn) | gnomAD v4 |
15 | g.73322774_73322775delinsGC | CA2187186686 | HCN4 | c.3318_3319delinsGC (p.Pro1106=) c.2100_2101delinsGC (p.Pro700=) | |
15 | g.73322775del | CA7648847 | HCN4 | c.3318del (p.His1107ThrfsTer?) c.2100del (p.His701ThrfsTer?) | dbSNP ExAC gnomAD v2 |
15 | g.73322775C>A | CA491477772 | HCN4 | c.3318G>T (p.Pro1106=) c.2100G>T (p.Pro700=) | gnomAD v4 |
15 | g.73322775C= | CA2187186690 | HCN4 | c.3318G= (p.Pro1106=) c.2100G= (p.Pro700=) | |
15 | g.73322775C>G | CA491477770 | HCN4 | c.3318G>C (p.Pro1106=) c.2100G>C (p.Pro700=) | |
15 | g.73322775C>T | CA491477771 | HCN4 | c.3318G>A (p.Pro1106=) c.2100G>A (p.Pro700=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73322776G>A | CA272663408 | HCN4 | c.3317C>T (p.Pro1106Leu) c.2099C>T (p.Pro700Leu) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73322776G>C | CA393085644 | HCN4 | c.3317C>G (p.Pro1106Arg) c.2099C>G (p.Pro700Arg) | gnomAD v4 |
15 | g.73322776G= | CA2187186693 | HCN4 | c.3317C= (p.Pro1106=) c.2099C= (p.Pro700=) | |
15 | g.73322776G>T | CA393085645 | HCN4 | c.3317C>A (p.Pro1106Gln) c.2099C>A (p.Pro700Gln) | gnomAD v4 |
15 | g.73322779del | CA2573151085 | HCN4 | c.3317del (p.Pro1106ArgfsTer?) c.2099del (p.Pro700ArgfsTer?) | ClinVar dbSNP |
15 | g.73322777G>A | CA393085647 | HCN4 | c.3316C>T (p.Pro1106Ser) c.2098C>T (p.Pro700Ser) | |
15 | g.73322777G>C | CA393085650 | HCN4 | c.3316C>G (p.Pro1106Ala) c.2098C>G (p.Pro700Ala) | |
15 | g.73322777G>T | CA393085652 | HCN4 | c.3316C>A (p.Pro1106Thr) c.2098C>A (p.Pro700Thr) | gnomAD v4 |
15 | g.73322778G>A | CA491477773 | HCN4 | c.3315C>T (p.Ser1105=) c.2097C>T (p.Ser699=) | ClinVar dbSNP gnomAD v4 |
15 | g.73322778G>C | CA491477774 | HCN4 | c.3315C>G (p.Ser1105=) c.2097C>G (p.Ser699=) | |
15 | g.73322778G= | CA2187186697 | HCN4 | c.3315C= (p.Ser1105=) c.2097C= (p.Ser699=) | |
15 | g.73322778G>T | CA491477775 | HCN4 | c.3315C>A (p.Ser1105=) c.2097C>A (p.Ser699=) | |
15 | g.73322778_73322779insC | CA2187186699 | HCN4 | c.3314_3315insG (p.His1107AlafsTer?) c.2096_2097insG (p.His701AlafsTer?) | dbSNP |
15 | g.73322779G>A | CA393085654 | HCN4 | c.3314C>T (p.Ser1105Phe) c.2096C>T (p.Ser699Phe) | gnomAD v4 |
15 | g.73322779G>C | CA393085656 | HCN4 | c.3314C>G (p.Ser1105Cys) c.2096C>G (p.Ser699Cys) | |
15 | g.73322779G= | CA2187186698 | HCN4 | c.3314C= (p.Ser1105=) c.2096C= (p.Ser699=) | |
15 | g.73322779G>T | CA393085657 | HCN4 | c.3314C>A (p.Ser1105Tyr) c.2096C>A (p.Ser699Tyr) | dbSNP gnomAD v2 |
15 | g.73322780A>C | CA393085664 | HCN4 | c.3313T>G (p.Ser1105Ala) c.2095T>G (p.Ser699Ala) | COSMIC |
15 | g.73322780A>G | CA393085661 | HCN4 | c.3313T>C (p.Ser1105Pro) c.2095T>C (p.Ser699Pro) | gnomAD v4 |
15 | g.73322780A>T | CA393085662 | HCN4 | c.3313T>A (p.Ser1105Thr) c.2095T>A (p.Ser699Thr) | |
15 | g.73322781G>A | CA491477776 | HCN4 | c.3312C>T (p.Ala1104=) c.2094C>T (p.Ala698=) | dbSNP |
15 | g.73322781G>C | CA491477777 | HCN4 | c.3312C>G (p.Ala1104=) c.2094C>G (p.Ala698=) | |
15 | g.73322781G>T | CA491477778 | HCN4 | c.3312C>A (p.Ala1104=) c.2094C>A (p.Ala698=) | |
15 | g.73322782G>A | CA393085666 | HCN4 | c.3311C>T (p.Ala1104Val) c.2093C>T (p.Ala698Val) | |
15 | g.73322782G>C | CA393085668 | HCN4 | c.3311C>G (p.Ala1104Gly) c.2093C>G (p.Ala698Gly) | |
15 | g.73322782G>T | CA393085670 | HCN4 | c.3311C>A (p.Ala1104Asp) c.2093C>A (p.Ala698Asp) | gnomAD v4 |
15 | g.73322783C>A | CA393085673 | HCN4 | c.3310G>T (p.Ala1104Ser) c.2092G>T (p.Ala698Ser) | gnomAD v4 |
15 | g.73322783C= | CA2187186703 | HCN4 | c.3310G= (p.Ala1104=) c.2092G= (p.Ala698=) | |
15 | g.73322783C>G | CA393085675 | HCN4 | c.3310G>C (p.Ala1104Pro) c.2092G>C (p.Ala698Pro) | |
15 | g.73322783C>T | CA7648848 | HCN4 | c.3310G>A (p.Ala1104Thr) c.2092G>A (p.Ala698Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73322784T>A | CA393085679 | HCN4 | c.3309A>T (p.Arg1103Ser) c.2091A>T (p.Arg697Ser) | |
15 | g.73322784T>C | CA491477779 | HCN4 | c.3309A>G (p.Arg1103=) c.2091A>G (p.Arg697=) | gnomAD v4 |
15 | g.73322784T>G | CA393085681 | HCN4 | c.3309A>C (p.Arg1103Ser) c.2091A>C (p.Arg697Ser) | |
15 | g.73322784_73322802delinsTCTGCGGAGAGTCTGCGCC | CA2187186704 | HCN4 | c.3291_3309delinsGGCGCAGACTCTCCGCAGA (p.Gly1097=) c.2073_2091delinsGGCGCAGACTCTCCGCAGA (p.Gly691=) | |
15 | g.73322785C>A | CA393085683 | HCN4 | c.3308G>T (p.Arg1103Ile) c.2090G>T (p.Arg697Ile) | gnomAD v4 |
15 | g.73322785C>G | CA393085686 | HCN4 | c.3308G>C (p.Arg1103Thr) c.2090G>C (p.Arg697Thr) |