Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.73332135A>C | CA393094236 | HCN4 | c.1367T>G (p.Met456Arg) c.149T>G (p.Met50Arg) | |
15 | g.73332135A>G | CA393094238 | HCN4 | c.1367T>C (p.Met456Thr) c.149T>C (p.Met50Thr) | |
15 | g.73332135A>T | CA393094237 | HCN4 | c.1367T>A (p.Met456Lys) c.149T>A (p.Met50Lys) | |
15 | g.73332136T>A | CA393094239 | HCN4 | c.1366A>T (p.Met456Leu) c.148A>T (p.Met50Leu) | |
15 | g.73332136T>C | CA393094240 | HCN4 | c.1366A>G (p.Met456Val) c.148A>G (p.Met50Val) | gnomAD v4 |
15 | g.73332136T>G | CA393094241 | HCN4 | c.1366A>C (p.Met456Leu) c.148A>C (p.Met50Leu) | |
15 | g.73332137G>A | CA491152522 | HCN4 | c.1365C>T (p.Asn455=) c.147C>T (p.Asn49=) | gnomAD v4 |
15 | g.73332137G>C | CA393094242 | HCN4 | c.1365C>G (p.Asn455Lys) c.147C>G (p.Asn49Lys) | |
15 | g.73332137G>T | CA393094243 | HCN4 | c.1365C>A (p.Asn455Lys) c.147C>A (p.Asn49Lys) | |
15 | g.73332138T>A | CA393094244 | HCN4 | c.1364A>T (p.Asn455Ile) c.146A>T (p.Asn49Ile) | |
15 | g.73332138T>C | CA393094245 | HCN4 | c.1364A>G (p.Asn455Ser) c.146A>G (p.Asn49Ser) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
15 | g.73332138T>G | CA393094246 | HCN4 | c.1364A>C (p.Asn455Thr) c.146A>C (p.Asn49Thr) | |
15 | g.73332138T= | CA2187169712 | HCN4 | c.1364A= (p.Asn455=) c.146A= (p.Asn49=) | |
15 | g.73332138_73332140delinsTTG | CA2187169714 | HCN4 | c.1362_1364delinsCAA (p.Asn454=) c.144_146delinsCAA (p.Asn48=) | |
15 | g.73332139T>A | CA393094247 | HCN4 | c.1363A>T (p.Asn455Tyr) c.145A>T (p.Asn49Tyr) | |
15 | g.73332139T>C | CA393094248 | HCN4 | c.1363A>G (p.Asn455Asp) c.145A>G (p.Asn49Asp) | dbSNP |
15 | g.73332139T>G | CA393094249 | HCN4 | c.1363A>C (p.Asn455His) c.145A>C (p.Asn49His) | |
15 | g.73332139T= | CA2187169718 | HCN4 | c.1363A= (p.Asn455=) c.145A= (p.Asn49=) | |
15 | g.73332140_73332141del | CA971407310 | HCN4 | c.1362_1363del (p.Asn454LysfsTer?) c.144_145del (p.Asn48LysfsTer?) | dbSNP gnomAD v3 gnomAD v4 |
15 | g.73332140G>A | CA491152523 | HCN4 | c.1362C>T (p.Asn454=) c.144C>T (p.Asn48=) | |
15 | g.73332140G>C | CA393094250 | HCN4 | c.1362C>G (p.Asn454Lys) c.144C>G (p.Asn48Lys) | |
15 | g.73332140G>T | CA393094251 | HCN4 | c.1362C>A (p.Asn454Lys) c.144C>A (p.Asn48Lys) | |
15 | g.73332141T>A | CA393094252 | HCN4 | c.1361A>T (p.Asn454Ile) c.143A>T (p.Asn48Ile) | |
15 | g.73332141T>C | CA393094253 | HCN4 | c.1361A>G (p.Asn454Ser) c.143A>G (p.Asn48Ser) | |
15 | g.73332141T>G | CA393094254 | HCN4 | c.1361A>C (p.Asn454Thr) c.143A>C (p.Asn48Thr) | |
15 | g.73332142T>A | CA393094255 | HCN4 | c.1360A>T (p.Asn454Tyr) c.142A>T (p.Asn48Tyr) | |
15 | g.73332142T>C | CA393094256 | HCN4 | c.1360A>G (p.Asn454Asp) c.142A>G (p.Asn48Asp) | dbSNP |
15 | g.73332142T>G | CA393094257 | HCN4 | c.1360A>C (p.Asn454His) c.142A>C (p.Asn48His) | |
15 | g.73332142T= | CA2187169722 | HCN4 | c.1360A= (p.Asn454=) c.142A= (p.Asn48=) | |
15 | g.73332143G>A | CA491152524 | HCN4 | c.1359C>T (p.Ile453=) c.141C>T (p.Ile47=) | |
15 | g.73332143G>C | CA393094258 | HCN4 | c.1359C>G (p.Ile453Met) c.141C>G (p.Ile47Met) | |
15 | g.73332143G>T | CA491152525 | HCN4 | c.1359C>A (p.Ile453=) c.141C>A (p.Ile47=) | |
15 | g.73332144A>C | CA393094259 | HCN4 | c.1358T>G (p.Ile453Ser) c.140T>G (p.Ile47Ser) | |
15 | g.73332144A>G | CA393094260 | HCN4 | c.1358T>C (p.Ile453Thr) c.140T>C (p.Ile47Thr) | |
15 | g.73332144A>T | CA393094261 | HCN4 | c.1358T>A (p.Ile453Asn) c.140T>A (p.Ile47Asn) | |
15 | g.73332145T>A | CA393094263 | HCN4 | c.1357A>T (p.Ile453Phe) c.139A>T (p.Ile47Phe) | |
15 | g.73332145T>C | CA393094264 | HCN4 | c.1357A>G (p.Ile453Val) c.139A>G (p.Ile47Val) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
15 | g.73332145T>G | CA393094262 | HCN4 | c.1357A>C (p.Ile453Leu) c.139A>C (p.Ile47Leu) | |
15 | g.73332145T= | CA2187169726 | HCN4 | c.1357A= (p.Ile453=) c.139A= (p.Ile47=) | |
15 | g.73332146G>A | CA7649323 | HCN4 | c.1356C>T (p.Ser452=) c.138C>T (p.Ser46=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73332146G>C | CA491152526 | HCN4 | c.1356C>G (p.Ser452=) c.138C>G (p.Ser46=) | |
15 | g.73332146G= | CA2187169730 | HCN4 | c.1356C= (p.Ser452=) c.138C= (p.Ser46=) | |
15 | g.73332146G>T | CA491152527 | HCN4 | c.1356C>A (p.Ser452=) c.138C>A (p.Ser46=) | |
15 | g.73332147G>A | CA393094265 | HCN4 | c.1355C>T (p.Ser452Phe) c.137C>T (p.Ser46Phe) | gnomAD v4 |
15 | g.73332147G>C | CA393094266 | HCN4 | c.1355C>G (p.Ser452Cys) c.137C>G (p.Ser46Cys) | |
15 | g.73332147G>T | CA393094267 | HCN4 | c.1355C>A (p.Ser452Tyr) c.137C>A (p.Ser46Tyr) | |
15 | g.73332148A>C | CA393094268 | HCN4 | c.1354T>G (p.Ser452Ala) c.136T>G (p.Ser46Ala) | |
15 | g.73332148A>G | CA393094269 | HCN4 | c.1354T>C (p.Ser452Pro) c.136T>C (p.Ser46Pro) | |
15 | g.73332148A>T | CA393094270 | HCN4 | c.1354T>A (p.Ser452Thr) c.136T>A (p.Ser46Thr) | gnomAD v4 |
15 | g.73332149C>A | CA7649324 | HCN4 | c.1353G>T (p.Val451=) c.135G>T (p.Val45=) | dbSNP ExAC gnomAD v2 gnomAD v4 |