Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.73323720C>A | CA7649039 | HCN4 | c.2373G>T (p.Val791=) c.1155G>T (p.Val385=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73323720C= | CA2187188621 | HCN4 | c.2373G= (p.Val791=) c.1155G= (p.Val385=) | |
15 | g.73323720C>G | CA491478554 | HCN4 | c.2373G>C (p.Val791=) c.1155G>C (p.Val385=) | |
15 | g.73323720C>T | CA491478555 | HCN4 | c.2373G>A (p.Val791=) c.1155G>A (p.Val385=) | |
15 | g.73323721A>C | CA393089018 | HCN4 | c.2372T>G (p.Val791Gly) c.1154T>G (p.Val385Gly) | |
15 | g.73323721A>G | CA393089020 | HCN4 | c.2372T>C (p.Val791Ala) c.1154T>C (p.Val385Ala) | |
15 | g.73323721A>T | CA393089019 | HCN4 | c.2372T>A (p.Val791Glu) c.1154T>A (p.Val385Glu) | gnomAD v4 |
15 | g.73323722C>A | CA393089021 | HCN4 | c.2371G>T (p.Val791Leu) c.1153G>T (p.Val385Leu) | |
15 | g.73323722C= | CA2187188622 | HCN4 | c.2371G= (p.Val791=) c.1153G= (p.Val385=) | |
15 | g.73323722C>G | CA393089022 | HCN4 | c.2371G>C (p.Val791Leu) c.1153G>C (p.Val385Leu) | |
15 | g.73323722C>T | CA272664876 | HCN4 | c.2371G>A (p.Val791Met) c.1153G>A (p.Val385Met) | dbSNP gnomAD v3 gnomAD v4 |
15 | g.73323723A= | CA2187188623 | HCN4 | c.2370T= (p.Ser790=) c.1152T= (p.Ser384=) | |
15 | g.73323723A>C | CA491478558 | HCN4 | c.2370T>G (p.Ser790=) c.1152T>G (p.Ser384=) | |
15 | g.73323723A>G | CA7649040 | HCN4 | c.2370T>C (p.Ser790=) c.1152T>C (p.Ser384=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323723A>T | CA491478561 | HCN4 | c.2370T>A (p.Ser790=) c.1152T>A (p.Ser384=) | |
15 | g.73323724G>A | CA393089023 | HCN4 | c.2369C>T (p.Ser790Phe) c.1151C>T (p.Ser384Phe) | |
15 | g.73323724G>C | CA393089024 | HCN4 | c.2369C>G (p.Ser790Cys) c.1151C>G (p.Ser384Cys) | |
15 | g.73323724G>T | CA393089025 | HCN4 | c.2369C>A (p.Ser790Tyr) c.1151C>A (p.Ser384Tyr) | gnomAD v4 COSMIC |
15 | g.73323725A= | CA2187188624 | HCN4 | c.2368T= (p.Ser790=) c.1150T= (p.Ser384=) | |
15 | g.73323725A>C | CA393089026 | HCN4 | c.2368T>G (p.Ser790Ala) c.1150T>G (p.Ser384Ala) | |
15 | g.73323725A>G | CA393089027 | HCN4 | c.2368T>C (p.Ser790Pro) c.1150T>C (p.Ser384Pro) | dbSNP gnomAD v3 gnomAD v4 |
15 | g.73323725A>T | CA393089028 | HCN4 | c.2368T>A (p.Ser790Thr) c.1150T>A (p.Ser384Thr) | |
15 | g.73323726A>C | CA491478564 | HCN4 | c.2367T>G (p.Thr789=) c.1149T>G (p.Thr383=) | |
15 | g.73323726A>G | CA491478565 | HCN4 | c.2367T>C (p.Thr789=) c.1149T>C (p.Thr383=) | |
15 | g.73323726A>T | CA491478566 | HCN4 | c.2367T>A (p.Thr789=) c.1149T>A (p.Thr383=) | |
15 | g.73323727G>A | CA393089029 | HCN4 | c.2366C>T (p.Thr789Ile) c.1148C>T (p.Thr383Ile) | |
15 | g.73323727G>C | CA393089030 | HCN4 | c.2366C>G (p.Thr789Ser) c.1148C>G (p.Thr383Ser) | |
15 | g.73323727G>T | CA393089031 | HCN4 | c.2366C>A (p.Thr789Asn) c.1148C>A (p.Thr383Asn) | gnomAD v4 |
15 | g.73323728T>A | CA393089032 | HCN4 | c.2365A>T (p.Thr789Ser) c.1147A>T (p.Thr383Ser) | |
15 | g.73323728T>C | CA393089033 | HCN4 | c.2365A>G (p.Thr789Ala) c.1147A>G (p.Thr383Ala) | gnomAD v4 |
15 | g.73323728T>G | CA393089034 | HCN4 | c.2365A>C (p.Thr789Pro) c.1147A>C (p.Thr383Pro) | |
15 | g.73323729G>A | CA491478575 | HCN4 | c.2364C>T (p.Thr788=) c.1146C>T (p.Thr382=) | gnomAD v4 |
15 | g.73323729G>C | CA491478576 | HCN4 | c.2364C>G (p.Thr788=) c.1146C>G (p.Thr382=) | |
15 | g.73323729G>T | CA491478577 | HCN4 | c.2364C>A (p.Thr788=) c.1146C>A (p.Thr382=) | gnomAD v4 |
15 | g.73323730G>A | CA393089037 | HCN4 | c.2363C>T (p.Thr788Ile) c.1145C>T (p.Thr382Ile) | gnomAD v4 |
15 | g.73323730G>C | CA393089035 | HCN4 | c.2363C>G (p.Thr788Ser) c.1145C>G (p.Thr382Ser) | |
15 | g.73323730G>T | CA393089036 | HCN4 | c.2363C>A (p.Thr788Asn) c.1145C>A (p.Thr382Asn) | gnomAD v4 |
15 | g.73323731T>A | CA393089038 | HCN4 | c.2362A>T (p.Thr788Ser) c.1144A>T (p.Thr382Ser) | |
15 | g.73323731T>C | CA393089039 | HCN4 | c.2362A>G (p.Thr788Ala) c.1144A>G (p.Thr382Ala) | gnomAD v4 |
15 | g.73323731T>G | CA393089040 | HCN4 | c.2362A>C (p.Thr788Pro) c.1144A>C (p.Thr382Pro) | |
15 | g.73323732G>A | CA491478578 | HCN4 | c.2361C>T (p.Ala787=) c.1143C>T (p.Ala381=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
15 | g.73323732G>C | CA491478581 | HCN4 | c.2361C>G (p.Ala787=) c.1143C>G (p.Ala381=) | |
15 | g.73323732G= | CA2187188625 | HCN4 | c.2361C= (p.Ala787=) c.1143C= (p.Ala381=) | |
15 | g.73323732G>T | CA491478582 | HCN4 | c.2361C>A (p.Ala787=) c.1143C>A (p.Ala381=) | gnomAD v4 |
15 | g.73323733G>A | CA393089041 | HCN4 | c.2360C>T (p.Ala787Val) c.1142C>T (p.Ala381Val) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323733G>C | CA393089042 | HCN4 | c.2360C>G (p.Ala787Gly) c.1142C>G (p.Ala381Gly) | |
15 | g.73323733G= | CA2187188626 | HCN4 | c.2360C= (p.Ala787=) c.1142C= (p.Ala381=) | |
15 | g.73323733G>T | CA393089043 | HCN4 | c.2360C>A (p.Ala787Asp) c.1142C>A (p.Ala381Asp) | gnomAD v4 |
15 | g.73323734C>A | CA393089044 | HCN4 | c.2359G>T (p.Ala787Ser) c.1141G>T (p.Ala381Ser) | ClinVar gnomAD v4 |
15 | g.73323734C>G | CA393089045 | HCN4 | c.2359G>C (p.Ala787Pro) c.1141G>C (p.Ala381Pro) |