| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 16 | g.89268645G>A | CA204730 | ANKRD11 | c.7825C>T (p.Gln2609Ter) c.*7628C>T (n.*7628C>T) c.1099C>T (p.Gln367Ter) c.506C>T c.7723C>T (p.Gln2575Ter) c.7528C>T (p.Gln2510Ter) c.7696C>T (p.Gln2566Ter) | ClinVar dbSNP gnomAD v4 |
| 16 | g.89268645G>C | CA397145355 | ANKRD11 | c.7825C>G (p.Gln2609Glu) c.*7628C>G (n.*7628C>G) c.1099C>G (p.Gln367Glu) c.506C>G c.7723C>G (p.Gln2575Glu) c.7528C>G (p.Gln2510Glu) c.7696C>G (p.Gln2566Glu) | |
| 16 | g.89268645G= | CA2241594820 | ANKRD11 | c.7825C= (p.Gln2609=) c.*7628C= (n.*7628C=) c.1099C= (p.Gln367=) c.506C= c.7723C= (p.Gln2575=) c.7528C= (p.Gln2510=) c.7696C= (p.Gln2566=) | |
| 16 | g.89268645G>T | CA397145357 | ANKRD11 | c.7825C>A (p.Gln2609Lys) c.*7628C>A (n.*7628C>A) c.1099C>A (p.Gln367Lys) c.506C>A c.7723C>A (p.Gln2575Lys) c.7528C>A (p.Gln2510Lys) c.7696C>A (p.Gln2566Lys) | gnomAD v4 |
| 16 | g.89268646C>A | CA497165721 | ANKRD11 | c.7824G>T (p.Arg2608=) c.*7627G>T (n.*7627G>T) c.1098G>T (p.Arg366=) c.505G>T c.7722G>T (p.Arg2574=) c.7527G>T (p.Arg2509=) c.7695G>T (p.Arg2565=) | gnomAD v4 |
| 16 | g.89268646C>G | CA497165724 | ANKRD11 | c.7824G>C (p.Arg2608=) c.*7627G>C (n.*7627G>C) c.1098G>C (p.Arg366=) c.505G>C c.7722G>C (p.Arg2574=) c.7527G>C (p.Arg2509=) c.7695G>C (p.Arg2565=) | |
| 16 | g.89268646C>T | CA497165723 | ANKRD11 | c.7824G>A (p.Arg2608=) c.*7627G>A (n.*7627G>A) c.1098G>A (p.Arg366=) c.505G>A c.7722G>A (p.Arg2574=) c.7527G>A (p.Arg2509=) c.7695G>A (p.Arg2565=) | gnomAD v4 |
| 16 | g.89268647C>A | CA397145359 | ANKRD11 | c.7823G>T (p.Arg2608Leu) c.*7626G>T (n.*7626G>T) c.1097G>T (p.Arg366Leu) c.504G>T c.7721G>T (p.Arg2574Leu) c.7526G>T (p.Arg2509Leu) c.7694G>T (p.Arg2565Leu) | gnomAD v4 |
| 16 | g.89268647C= | CA2241594821 | ANKRD11 | c.7823G= (p.Arg2608=) c.*7626G= (n.*7626G=) c.1097G= (p.Arg366=) c.504G= c.7721G= (p.Arg2574=) c.7526G= (p.Arg2509=) c.7694G= (p.Arg2565=) | |
| 16 | g.89268647C>G | CA397145361 | ANKRD11 | c.7823G>C (p.Arg2608Pro) c.*7626G>C (n.*7626G>C) c.1097G>C (p.Arg366Pro) c.504G>C c.7721G>C (p.Arg2574Pro) c.7526G>C (p.Arg2509Pro) c.7694G>C (p.Arg2565Pro) | |
| 16 | g.89268647C>T | CA397145363 | ANKRD11 | c.7823G>A (p.Arg2608Gln) c.*7626G>A (n.*7626G>A) c.1097G>A (p.Arg366Gln) c.504G>A c.7721G>A (p.Arg2574Gln) c.7526G>A (p.Arg2509Gln) c.7694G>A (p.Arg2565Gln) | dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 16 | g.89268648G>A | CA397145367 | ANKRD11 | c.7822C>T (p.Arg2608Trp) c.*7625C>T (n.*7625C>T) c.1096C>T (p.Arg366Trp) c.503C>T c.7720C>T (p.Arg2574Trp) c.7525C>T (p.Arg2509Trp) c.7693C>T (p.Arg2565Trp) | ClinVar dbSNP gnomAD v4 |
| 16 | g.89268648G>C | CA397145365 | ANKRD11 | c.7822C>G (p.Arg2608Gly) c.*7625C>G (n.*7625C>G) c.1096C>G (p.Arg366Gly) c.503C>G c.7720C>G (p.Arg2574Gly) c.7525C>G (p.Arg2509Gly) c.7693C>G (p.Arg2565Gly) | ClinVar |
| 16 | g.89268648G= | CA2241594822 | ANKRD11 | c.7822C= (p.Arg2608=) c.*7625C= (n.*7625C=) c.1096C= (p.Arg366=) c.503C= c.7720C= (p.Arg2574=) c.7525C= (p.Arg2509=) c.7693C= (p.Arg2565=) | |
| 16 | g.89268648G>T | CA497165730 | ANKRD11 | c.7822C>A (p.Arg2608=) c.*7625C>A (n.*7625C>A) c.1096C>A (p.Arg366=) c.503C>A c.7720C>A (p.Arg2574=) c.7525C>A (p.Arg2509=) c.7693C>A (p.Arg2565=) | gnomAD v4 |
| 16 | g.89268649C>A | CA397145369 | ANKRD11 | c.7821G>T (p.Met2607Ile) c.*7624G>T (n.*7624G>T) c.1095G>T (p.Met365Ile) c.502G>T c.7719G>T (p.Met2573Ile) c.7524G>T (p.Met2508Ile) c.7692G>T (p.Met2564Ile) | |
| 16 | g.89268649C>G | CA397145371 | ANKRD11 | c.7821G>C (p.Met2607Ile) c.*7624G>C (n.*7624G>C) c.1095G>C (p.Met365Ile) c.502G>C c.7719G>C (p.Met2573Ile) c.7524G>C (p.Met2508Ile) c.7692G>C (p.Met2564Ile) | |
| 16 | g.89268649C>T | CA397145373 | ANKRD11 | c.7821G>A (p.Met2607Ile) c.*7624G>A (n.*7624G>A) c.1095G>A (p.Met365Ile) c.502G>A c.7719G>A (p.Met2573Ile) c.7524G>A (p.Met2508Ile) c.7692G>A (p.Met2564Ile) | |
| 16 | g.89268650A>C | CA397145375 | ANKRD11 | c.7820T>G (p.Met2607Arg) c.*7623T>G (n.*7623T>G) c.1094T>G (p.Met365Arg) c.501T>G c.7718T>G (p.Met2573Arg) c.7523T>G (p.Met2508Arg) c.7691T>G (p.Met2564Arg) | |
| 16 | g.89268650A>G | CA397145377 | ANKRD11 | c.7820T>C (p.Met2607Thr) c.*7623T>C (n.*7623T>C) c.1094T>C (p.Met365Thr) c.501T>C c.7718T>C (p.Met2573Thr) c.7523T>C (p.Met2508Thr) c.7691T>C (p.Met2564Thr) | |
| 16 | g.89268650A>T | CA397145379 | ANKRD11 | c.7820T>A (p.Met2607Lys) c.*7623T>A (n.*7623T>A) c.1094T>A (p.Met365Lys) c.501T>A c.7718T>A (p.Met2573Lys) c.7523T>A (p.Met2508Lys) c.7691T>A (p.Met2564Lys) | |
| 16 | g.89268651T>A | CA397145380 | ANKRD11 | c.7819A>T (p.Met2607Leu) c.*7622A>T (n.*7622A>T) c.1093A>T (p.Met365Leu) c.500A>T c.7717A>T (p.Met2573Leu) c.7522A>T (p.Met2508Leu) c.7690A>T (p.Met2564Leu) | |
| 16 | g.89268651T>C | CA397145384 | ANKRD11 | c.7819A>G (p.Met2607Val) c.*7622A>G (n.*7622A>G) c.1093A>G (p.Met365Val) c.500A>G c.7717A>G (p.Met2573Val) c.7522A>G (p.Met2508Val) c.7690A>G (p.Met2564Val) | dbSNP gnomAD v4 |
| 16 | g.89268651T>G | CA397145382 | ANKRD11 | c.7819A>C (p.Met2607Leu) c.*7622A>C (n.*7622A>C) c.1093A>C (p.Met365Leu) c.500A>C c.7717A>C (p.Met2573Leu) c.7522A>C (p.Met2508Leu) c.7690A>C (p.Met2564Leu) | |
| 16 | g.89268651T= | CA2241594823 | ANKRD11 | c.7819A= (p.Met2607=) c.*7622A= (n.*7622A=) c.1093A= (p.Met365=) c.500A= c.7717A= (p.Met2573=) c.7522A= (p.Met2508=) c.7690A= (p.Met2564=) | |
| 16 | g.89268652G>A | CA497165741 | ANKRD11 | c.7818C>T (p.Leu2606=) c.*7621C>T (n.*7621C>T) c.1092C>T (p.Leu364=) c.499C>T c.7716C>T (p.Leu2572=) c.7521C>T (p.Leu2507=) c.7689C>T (p.Leu2563=) | |
| 16 | g.89268652G>C | CA497165746 | ANKRD11 | c.7818C>G (p.Leu2606=) c.*7621C>G (n.*7621C>G) c.1092C>G (p.Leu364=) c.499C>G c.7716C>G (p.Leu2572=) c.7521C>G (p.Leu2507=) c.7689C>G (p.Leu2563=) | |
| 16 | g.89268652G>T | CA497165748 | ANKRD11 | c.7818C>A (p.Leu2606=) c.*7621C>A (n.*7621C>A) c.1092C>A (p.Leu364=) c.499C>A c.7716C>A (p.Leu2572=) c.7521C>A (p.Leu2507=) c.7689C>A (p.Leu2563=) | gnomAD v4 |
| 16 | g.89268656_89268658del | CA2580613925 | ANKRD11 | c.7816_7818del (p.Leu2606del) c.*7619_*7621del (n.*7619_*7621del) c.1090_1092del (p.Leu364del) c.497_499del c.7714_7716del (p.Leu2572del) c.7519_7521del (p.Leu2507del) c.7687_7689del (p.Leu2563del) | ClinVar dbSNP |
| 16 | g.89268653A= | CA2241594824 | ANKRD11 | c.7817T= (p.Leu2606=) c.*7620T= (n.*7620T=) c.1091T= (p.Leu364=) c.498T= c.7715T= (p.Leu2572=) c.7520T= (p.Leu2507=) c.7688T= (p.Leu2563=) | |
| 16 | g.89268653A>C | CA397145386 | ANKRD11 | c.7817T>G (p.Leu2606Arg) c.*7620T>G (n.*7620T>G) c.1091T>G (p.Leu364Arg) c.498T>G c.7715T>G (p.Leu2572Arg) c.7520T>G (p.Leu2507Arg) c.7688T>G (p.Leu2563Arg) | |
| 16 | g.89268653A>G | CA286503932 | ANKRD11 | c.7817T>C (p.Leu2606Pro) c.*7620T>C (n.*7620T>C) c.1091T>C (p.Leu364Pro) c.498T>C c.7715T>C (p.Leu2572Pro) c.7520T>C (p.Leu2507Pro) c.7688T>C (p.Leu2563Pro) | dbSNP gnomAD v4 |
| 16 | g.89268653A>T | CA397145389 | ANKRD11 | c.7817T>A (p.Leu2606His) c.*7620T>A (n.*7620T>A) c.1091T>A (p.Leu364His) c.498T>A c.7715T>A (p.Leu2572His) c.7520T>A (p.Leu2507His) c.7688T>A (p.Leu2563His) | gnomAD v4 |
| 16 | g.89268654G>A | CA397145391 | ANKRD11 | c.7816C>T (p.Leu2606Phe) c.*7619C>T (n.*7619C>T) c.1090C>T (p.Leu364Phe) c.497C>T c.7714C>T (p.Leu2572Phe) c.7519C>T (p.Leu2507Phe) c.7687C>T (p.Leu2563Phe) | gnomAD v4 |
| 16 | g.89268654G>C | CA397145393 | ANKRD11 | c.7816C>G (p.Leu2606Val) c.*7619C>G (n.*7619C>G) c.1090C>G (p.Leu364Val) c.497C>G c.7714C>G (p.Leu2572Val) c.7519C>G (p.Leu2507Val) c.7687C>G (p.Leu2563Val) | |
| 16 | g.89268654G>T | CA397145395 | ANKRD11 | c.7816C>A (p.Leu2606Ile) c.*7619C>A (n.*7619C>A) c.1090C>A (p.Leu364Ile) c.497C>A c.7714C>A (p.Leu2572Ile) c.7519C>A (p.Leu2507Ile) c.7687C>A (p.Leu2563Ile) | gnomAD v4 |
| 16 | g.89268655G>A | CA8240983 | ANKRD11 | c.7815C>T (p.Leu2605=) c.*7618C>T (n.*7618C>T) c.1089C>T (p.Leu363=) c.496C>T c.7713C>T (p.Leu2571=) c.7518C>T (p.Leu2506=) c.7686C>T (p.Leu2562=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.89268655G>C | CA497165753 | ANKRD11 | c.7815C>G (p.Leu2605=) c.*7618C>G (n.*7618C>G) c.1089C>G (p.Leu363=) c.496C>G c.7713C>G (p.Leu2571=) c.7518C>G (p.Leu2506=) c.7686C>G (p.Leu2562=) | gnomAD v4 |
| 16 | g.89268655G= | CA2241594825 | ANKRD11 | c.7815C= (p.Leu2605=) c.*7618C= (n.*7618C=) c.1089C= (p.Leu363=) c.496C= c.7713C= (p.Leu2571=) c.7518C= (p.Leu2506=) c.7686C= (p.Leu2562=) | |
| 16 | g.89268655G>T | CA497165754 | ANKRD11 | c.7815C>A (p.Leu2605=) c.*7618C>A (n.*7618C>A) c.1089C>A (p.Leu363=) c.496C>A c.7713C>A (p.Leu2571=) c.7518C>A (p.Leu2506=) c.7686C>A (p.Leu2562=) | gnomAD v4 |
| 16 | g.89268656A= | CA2241594826 | ANKRD11 | c.7814T= (p.Leu2605=) c.*7617T= (n.*7617T=) c.1088T= (p.Leu363=) c.495T= c.7712T= (p.Leu2571=) c.7517T= (p.Leu2506=) c.7685T= (p.Leu2562=) | |
| 16 | g.89268656A>C | CA397145398 | ANKRD11 | c.7814T>G (p.Leu2605Arg) c.*7617T>G (n.*7617T>G) c.1088T>G (p.Leu363Arg) c.495T>G c.7712T>G (p.Leu2571Arg) c.7517T>G (p.Leu2506Arg) c.7685T>G (p.Leu2562Arg) | ClinVar dbSNP |
| 16 | g.89268656A>G | CA397145400 | ANKRD11 | c.7814T>C (p.Leu2605Pro) c.*7617T>C (n.*7617T>C) c.1088T>C (p.Leu363Pro) c.495T>C c.7712T>C (p.Leu2571Pro) c.7517T>C (p.Leu2506Pro) c.7685T>C (p.Leu2562Pro) | gnomAD v4 |
| 16 | g.89268656A>T | CA397145401 | ANKRD11 | c.7814T>A (p.Leu2605His) c.*7617T>A (n.*7617T>A) c.1088T>A (p.Leu363His) c.495T>A c.7712T>A (p.Leu2571His) c.7517T>A (p.Leu2506His) c.7685T>A (p.Leu2562His) | gnomAD v4 |
| 16 | g.89268657G>A | CA397145403 | ANKRD11 | c.7813C>T (p.Leu2605Phe) c.*7616C>T (n.*7616C>T) c.1087C>T (p.Leu363Phe) c.494C>T c.7711C>T (p.Leu2571Phe) c.7516C>T (p.Leu2506Phe) c.7684C>T (p.Leu2562Phe) | |
| 16 | g.89268657G>C | CA397145405 | ANKRD11 | c.7813C>G (p.Leu2605Val) c.*7616C>G (n.*7616C>G) c.1087C>G (p.Leu363Val) c.494C>G c.7711C>G (p.Leu2571Val) c.7516C>G (p.Leu2506Val) c.7684C>G (p.Leu2562Val) | gnomAD v4 |
| 16 | g.89268657G>T | CA397145406 | ANKRD11 | c.7813C>A (p.Leu2605Ile) c.*7616C>A (n.*7616C>A) c.1087C>A (p.Leu363Ile) c.494C>A c.7711C>A (p.Leu2571Ile) c.7516C>A (p.Leu2506Ile) c.7684C>A (p.Leu2562Ile) | gnomAD v4 |
| 16 | g.89268658G>A | CA497165763 | ANKRD11 | c.7812C>T (p.Cys2604=) c.*7615C>T (n.*7615C>T) c.1086C>T (p.Cys362=) c.493C>T c.7710C>T (p.Cys2570=) c.7515C>T (p.Cys2505=) c.7683C>T (p.Cys2561=) | dbSNP gnomAD v4 |
| 16 | g.89268658G>C | CA397145409 | ANKRD11 | c.7812C>G (p.Cys2604Trp) c.*7615C>G (n.*7615C>G) c.1086C>G (p.Cys362Trp) c.493C>G c.7710C>G (p.Cys2570Trp) c.7515C>G (p.Cys2505Trp) c.7683C>G (p.Cys2561Trp) | |
| 16 | g.89268658G= | CA2241594827 | ANKRD11 | c.7812C= (p.Cys2604=) c.*7615C= (n.*7615C=) c.1086C= (p.Cys362=) c.493C= c.7710C= (p.Cys2570=) c.7515C= (p.Cys2505=) c.7683C= (p.Cys2561=) |