Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.73323570C>A | CA491478227 | HCN4 | c.2523G>T (p.Ser841=) c.1305G>T (p.Ser435=) | ClinVar dbSNP |
15 | g.73323570C= | CA2187188543 | HCN4 | c.2523G= (p.Ser841=) c.1305G= (p.Ser435=) | |
15 | g.73323570C>G | CA491478228 | HCN4 | c.2523G>C (p.Ser841=) c.1305G>C (p.Ser435=) | |
15 | g.73323570C>T | CA247657 | HCN4 | c.2523G>A (p.Ser841=) c.1305G>A (p.Ser435=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323571G>A | CA235703 | HCN4 | c.2522C>T (p.Ser841Leu) c.1304C>T (p.Ser435Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323571G>C | CA393088734 | HCN4 | c.2522C>G (p.Ser841Trp) c.1304C>G (p.Ser435Trp) | |
15 | g.73323571G= | CA2187188544 | HCN4 | c.2522C= (p.Ser841=) c.1304C= (p.Ser435=) | |
15 | g.73323571G>T | CA393088733 | HCN4 | c.2522C>A (p.Ser841Ter) c.1304C>A (p.Ser435Ter) | |
15 | g.73323572A>C | CA393088735 | HCN4 | c.2521T>G (p.Ser841Ala) c.1303T>G (p.Ser435Ala) | |
15 | g.73323572A>G | CA393088736 | HCN4 | c.2521T>C (p.Ser841Pro) c.1303T>C (p.Ser435Pro) | |
15 | g.73323572A>T | CA393088737 | HCN4 | c.2521T>A (p.Ser841Thr) c.1303T>A (p.Ser435Thr) | |
15 | g.73323573G>A | CA491478232 | HCN4 | c.2520C>T (p.Ala840=) c.1302C>T (p.Ala434=) | |
15 | g.73323573G>C | CA491478234 | HCN4 | c.2520C>G (p.Ala840=) c.1302C>G (p.Ala434=) | |
15 | g.73323573G>T | CA491478233 | HCN4 | c.2520C>A (p.Ala840=) c.1302C>A (p.Ala434=) | |
15 | g.73323574G>A | CA393088738 | HCN4 | c.2519C>T (p.Ala840Val) c.1301C>T (p.Ala434Val) | |
15 | g.73323574G>C | CA393088739 | HCN4 | c.2519C>G (p.Ala840Gly) c.1301C>G (p.Ala434Gly) | |
15 | g.73323574G>T | CA393088740 | HCN4 | c.2519C>A (p.Ala840Asp) c.1301C>A (p.Ala434Asp) | |
15 | g.73323575C>A | CA393088741 | HCN4 | c.2518G>T (p.Ala840Ser) c.1300G>T (p.Ala434Ser) | dbSNP gnomAD v4 |
15 | g.73323575C= | CA2187188545 | HCN4 | c.2518G= (p.Ala840=) c.1300G= (p.Ala434=) | |
15 | g.73323575C>G | CA7649008 | HCN4 | c.2518G>C (p.Ala840Pro) c.1300G>C (p.Ala434Pro) | dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73323575C>T | CA7649009 | HCN4 | c.2518G>A (p.Ala840Thr) c.1300G>A (p.Ala434Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323575_73323578dup | CA2580089986 | HCN4 | c.2515_2518dup (p.Ala840ValfsTer?) c.1297_1300dup (p.Ala434ValfsTer?) | ClinVar |
15 | g.73323576G>A | CA7649010 | HCN4 | c.2517C>T (p.Ser839=) c.1299C>T (p.Ser433=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323576G>C | CA491478238 | HCN4 | c.2517C>G (p.Ser839=) c.1299C>G (p.Ser433=) | |
15 | g.73323576G= | CA2187188546 | HCN4 | c.2517C= (p.Ser839=) c.1299C= (p.Ser433=) | |
15 | g.73323576G>T | CA491478239 | HCN4 | c.2517C>A (p.Ser839=) c.1299C>A (p.Ser433=) | |
15 | g.73323577G>A | CA393088742 | HCN4 | c.2516C>T (p.Ser839Phe) c.1298C>T (p.Ser433Phe) | |
15 | g.73323577G>C | CA393088743 | HCN4 | c.2516C>G (p.Ser839Cys) c.1298C>G (p.Ser433Cys) | |
15 | g.73323577G>T | CA393088744 | HCN4 | c.2516C>A (p.Ser839Tyr) c.1298C>A (p.Ser433Tyr) | |
15 | g.73323578A>C | CA393088747 | HCN4 | c.2515T>G (p.Ser839Ala) c.1297T>G (p.Ser433Ala) | gnomAD v4 |
15 | g.73323578A>G | CA393088746 | HCN4 | c.2515T>C (p.Ser839Pro) c.1297T>C (p.Ser433Pro) | |
15 | g.73323578A>T | CA393088745 | HCN4 | c.2515T>A (p.Ser839Thr) c.1297T>A (p.Ser433Thr) | |
15 | g.73323579G>A | CA491478241 | HCN4 | c.2514C>T (p.Gly838=) c.1296C>T (p.Gly432=) | dbSNP gnomAD v2 gnomAD v4 |
15 | g.73323579G>C | CA7649011 | HCN4 | c.2514C>G (p.Gly838=) c.1296C>G (p.Gly432=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323579G= | CA2187188547 | HCN4 | c.2514C= (p.Gly838=) c.1296C= (p.Gly432=) | |
15 | g.73323579G>T | CA491478243 | HCN4 | c.2514C>A (p.Gly838=) c.1296C>A (p.Gly432=) | |
15 | g.73323580C>A | CA393088748 | HCN4 | c.2513G>T (p.Gly838Val) c.1295G>T (p.Gly432Val) | |
15 | g.73323580C>G | CA393088749 | HCN4 | c.2513G>C (p.Gly838Ala) c.1295G>C (p.Gly432Ala) | |
15 | g.73323580C>T | CA393088750 | HCN4 | c.2513G>A (p.Gly838Asp) c.1295G>A (p.Gly432Asp) | gnomAD v4 |
15 | g.73323581C>A | CA393088751 | HCN4 | c.2512G>T (p.Gly838Cys) c.1294G>T (p.Gly432Cys) | |
15 | g.73323581C>G | CA393088752 | HCN4 | c.2512G>C (p.Gly838Arg) c.1294G>C (p.Gly432Arg) | ClinVar gnomAD v4 |
15 | g.73323581C>T | CA393088753 | HCN4 | c.2512G>A (p.Gly838Ser) c.1294G>A (p.Gly432Ser) | gnomAD v4 |
15 | g.73323582C>A | CA491478246 | HCN4 | c.2511G>T (p.Leu837=) c.1293G>T (p.Leu431=) | |
15 | g.73323582C>G | CA491478247 | HCN4 | c.2511G>C (p.Leu837=) c.1293G>C (p.Leu431=) | |
15 | g.73323582C>T | CA491478248 | HCN4 | c.2511G>A (p.Leu837=) c.1293G>A (p.Leu431=) | gnomAD v4 |
15 | g.73323583A>C | CA393088754 | HCN4 | c.2510T>G (p.Leu837Arg) c.1292T>G (p.Leu431Arg) | |
15 | g.73323583A>G | CA393088755 | HCN4 | c.2510T>C (p.Leu837Pro) c.1292T>C (p.Leu431Pro) | gnomAD v4 |
15 | g.73323583A>T | CA393088756 | HCN4 | c.2510T>A (p.Leu837Gln) c.1292T>A (p.Leu431Gln) | |
15 | g.73323584G>A | CA491478251 | HCN4 | c.2509C>T (p.Leu837=) c.1291C>T (p.Leu431=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
15 | g.73323584G>C | CA393088757 | HCN4 | c.2509C>G (p.Leu837Val) c.1291C>G (p.Leu431Val) |