| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 16 | g.89268545T>A | CA397145037 | ANKRD11 | c.7925A>T (p.Asn2642Ile) c.*7728A>T (n.*7728A>T) c.1199A>T (p.Asn400Ile) c.606A>T c.7823A>T (p.Asn2608Ile) c.7628A>T (p.Asn2543Ile) c.7796A>T (p.Asn2599Ile) | |
| 16 | g.89268545T>C | CA397145038 | ANKRD11 | c.7925A>G (p.Asn2642Ser) c.*7728A>G (n.*7728A>G) c.1199A>G (p.Asn400Ser) c.606A>G c.7823A>G (p.Asn2608Ser) c.7628A>G (p.Asn2543Ser) c.7796A>G (p.Asn2599Ser) | |
| 16 | g.89268545T>G | CA397145039 | ANKRD11 | c.7925A>C (p.Asn2642Thr) c.*7728A>C (n.*7728A>C) c.1199A>C (p.Asn400Thr) c.606A>C c.7823A>C (p.Asn2608Thr) c.7628A>C (p.Asn2543Thr) c.7796A>C (p.Asn2599Thr) | gnomAD v4 |
| 16 | g.89268546T>A | CA397145040 | ANKRD11 | c.7924A>T (p.Asn2642Tyr) c.*7727A>T (n.*7727A>T) c.1198A>T (p.Asn400Tyr) c.605A>T c.7822A>T (p.Asn2608Tyr) c.7627A>T (p.Asn2543Tyr) c.7795A>T (p.Asn2599Tyr) | |
| 16 | g.89268546T>C | CA397145041 | ANKRD11 | c.7924A>G (p.Asn2642Asp) c.*7727A>G (n.*7727A>G) c.1198A>G (p.Asn400Asp) c.605A>G c.7822A>G (p.Asn2608Asp) c.7627A>G (p.Asn2543Asp) c.7795A>G (p.Asn2599Asp) | |
| 16 | g.89268546T>G | CA397145042 | ANKRD11 | c.7924A>C (p.Asn2642His) c.*7727A>C (n.*7727A>C) c.1198A>C (p.Asn400His) c.605A>C c.7822A>C (p.Asn2608His) c.7627A>C (p.Asn2543His) c.7795A>C (p.Asn2599His) | |
| 16 | g.89268547C>A | CA497165599 | ANKRD11 | c.7923G>T (p.Val2641=) c.*7726G>T (n.*7726G>T) c.1197G>T (p.Val399=) c.604G>T c.7821G>T (p.Val2607=) c.7626G>T (p.Val2542=) c.7794G>T (p.Val2598=) | gnomAD v4 |
| 16 | g.89268547C>G | CA497165600 | ANKRD11 | c.7923G>C (p.Val2641=) c.*7726G>C (n.*7726G>C) c.1197G>C (p.Val399=) c.604G>C c.7821G>C (p.Val2607=) c.7626G>C (p.Val2542=) c.7794G>C (p.Val2598=) | |
| 16 | g.89268547C>T | CA497165601 | ANKRD11 | c.7923G>A (p.Val2641=) c.*7726G>A (n.*7726G>A) c.1197G>A (p.Val399=) c.604G>A c.7821G>A (p.Val2607=) c.7626G>A (p.Val2542=) c.7794G>A (p.Val2598=) | |
| 16 | g.89268548A>C | CA397145043 | ANKRD11 | c.7922T>G (p.Val2641Gly) c.*7725T>G (n.*7725T>G) c.1196T>G (p.Val399Gly) c.603T>G c.7820T>G (p.Val2607Gly) c.7625T>G (p.Val2542Gly) c.7793T>G (p.Val2598Gly) | |
| 16 | g.89268548A>G | CA397145044 | ANKRD11 | c.7922T>C (p.Val2641Ala) c.*7725T>C (n.*7725T>C) c.1196T>C (p.Val399Ala) c.603T>C c.7820T>C (p.Val2607Ala) c.7625T>C (p.Val2542Ala) c.7793T>C (p.Val2598Ala) | |
| 16 | g.89268548A>T | CA397145045 | ANKRD11 | c.7922T>A (p.Val2641Glu) c.*7725T>A (n.*7725T>A) c.1196T>A (p.Val399Glu) c.603T>A c.7820T>A (p.Val2607Glu) c.7625T>A (p.Val2542Glu) c.7793T>A (p.Val2598Glu) | |
| 16 | g.89268549C>A | CA397145046 | ANKRD11 | c.7921G>T (p.Val2641Leu) c.*7724G>T (n.*7724G>T) c.1195G>T (p.Val399Leu) c.602G>T c.7819G>T (p.Val2607Leu) c.7624G>T (p.Val2542Leu) c.7792G>T (p.Val2598Leu) | |
| 16 | g.89268549C>G | CA397145047 | ANKRD11 | c.7921G>C (p.Val2641Leu) c.*7724G>C (n.*7724G>C) c.1195G>C (p.Val399Leu) c.602G>C c.7819G>C (p.Val2607Leu) c.7624G>C (p.Val2542Leu) c.7792G>C (p.Val2598Leu) | |
| 16 | g.89268549C>T | CA397145048 | ANKRD11 | c.7921G>A (p.Val2641Met) c.*7724G>A (n.*7724G>A) c.1195G>A (p.Val399Met) c.602G>A c.7819G>A (p.Val2607Met) c.7624G>A (p.Val2542Met) c.7792G>A (p.Val2598Met) | ClinVar dbSNP gnomAD v4 |
| 16 | g.89268550G>A | CA497165602 | ANKRD11 | c.7920C>T (p.Cys2640=) c.*7723C>T (n.*7723C>T) c.1194C>T (p.Cys398=) c.601C>T c.7818C>T (p.Cys2606=) c.7623C>T (p.Cys2541=) c.7791C>T (p.Cys2597=) | dbSNP gnomAD v4 |
| 16 | g.89268550G>C | CA397145050 | ANKRD11 | c.7920C>G (p.Cys2640Trp) c.*7723C>G (n.*7723C>G) c.1194C>G (p.Cys398Trp) c.601C>G c.7818C>G (p.Cys2606Trp) c.7623C>G (p.Cys2541Trp) c.7791C>G (p.Cys2597Trp) | |
| 16 | g.89268550G= | CA2241594787 | ANKRD11 | c.7920C= (p.Cys2640=) c.*7723C= (n.*7723C=) c.1194C= (p.Cys398=) c.601C= c.7818C= (p.Cys2606=) c.7623C= (p.Cys2541=) c.7791C= (p.Cys2597=) | |
| 16 | g.89268550G>T | CA397145049 | ANKRD11 | c.7920C>A (p.Cys2640Ter) c.*7723C>A (n.*7723C>A) c.1194C>A (p.Cys398Ter) c.601C>A c.7818C>A (p.Cys2606Ter) c.7623C>A (p.Cys2541Ter) c.7791C>A (p.Cys2597Ter) | gnomAD v4 |
| 16 | g.89268551C>A | CA397145051 | ANKRD11 | c.7919G>T (p.Cys2640Phe) c.*7722G>T (n.*7722G>T) c.1193G>T (p.Cys398Phe) c.600G>T c.7817G>T (p.Cys2606Phe) c.7622G>T (p.Cys2541Phe) c.7790G>T (p.Cys2597Phe) | |
| 16 | g.89268551C>G | CA397145053 | ANKRD11 | c.7919G>C (p.Cys2640Ser) c.*7722G>C (n.*7722G>C) c.1193G>C (p.Cys398Ser) c.600G>C c.7817G>C (p.Cys2606Ser) c.7622G>C (p.Cys2541Ser) c.7790G>C (p.Cys2597Ser) | |
| 16 | g.89268551C>T | CA397145052 | ANKRD11 | c.7919G>A (p.Cys2640Tyr) c.*7722G>A (n.*7722G>A) c.1193G>A (p.Cys398Tyr) c.600G>A c.7817G>A (p.Cys2606Tyr) c.7622G>A (p.Cys2541Tyr) c.7790G>A (p.Cys2597Tyr) | |
| 16 | g.89268552A>C | CA397145054 | ANKRD11 | c.7918T>G (p.Cys2640Gly) c.*7721T>G (n.*7721T>G) c.1192T>G (p.Cys398Gly) c.599T>G c.7816T>G (p.Cys2606Gly) c.7621T>G (p.Cys2541Gly) c.7789T>G (p.Cys2597Gly) | |
| 16 | g.89268552A>G | CA397145056 | ANKRD11 | c.7918T>C (p.Cys2640Arg) c.*7721T>C (n.*7721T>C) c.1192T>C (p.Cys398Arg) c.599T>C c.7816T>C (p.Cys2606Arg) c.7621T>C (p.Cys2541Arg) c.7789T>C (p.Cys2597Arg) | |
| 16 | g.89268552A>T | CA397145055 | ANKRD11 | c.7918T>A (p.Cys2640Ser) c.*7721T>A (n.*7721T>A) c.1192T>A (p.Cys398Ser) c.599T>A c.7816T>A (p.Cys2606Ser) c.7621T>A (p.Cys2541Ser) c.7789T>A (p.Cys2597Ser) | |
| 16 | g.89268553C>A | CA497165604 | ANKRD11 | c.7917G>T (p.Leu2639=) c.*7720G>T (n.*7720G>T) c.1191G>T (p.Leu397=) c.598G>T c.7815G>T (p.Leu2605=) c.7620G>T (p.Leu2540=) c.7788G>T (p.Leu2596=) | |
| 16 | g.89268553C>G | CA497165606 | ANKRD11 | c.7917G>C (p.Leu2639=) c.*7720G>C (n.*7720G>C) c.1191G>C (p.Leu397=) c.598G>C c.7815G>C (p.Leu2605=) c.7620G>C (p.Leu2540=) c.7788G>C (p.Leu2596=) | gnomAD v4 |
| 16 | g.89268553C>T | CA497165608 | ANKRD11 | c.7917G>A (p.Leu2639=) c.*7720G>A (n.*7720G>A) c.1191G>A (p.Leu397=) c.598G>A c.7815G>A (p.Leu2605=) c.7620G>A (p.Leu2540=) c.7788G>A (p.Leu2596=) | |
| 16 | g.89268554A>C | CA397145057 | ANKRD11 | c.7916T>G (p.Leu2639Arg) c.*7719T>G (n.*7719T>G) c.1190T>G (p.Leu397Arg) c.597T>G c.7814T>G (p.Leu2605Arg) c.7619T>G (p.Leu2540Arg) c.7787T>G (p.Leu2596Arg) | |
| 16 | g.89268554A>G | CA397145058 | ANKRD11 | c.7916T>C (p.Leu2639Pro) c.*7719T>C (n.*7719T>C) c.1190T>C (p.Leu397Pro) c.597T>C c.7814T>C (p.Leu2605Pro) c.7619T>C (p.Leu2540Pro) c.7787T>C (p.Leu2596Pro) | |
| 16 | g.89268554A>T | CA397145059 | ANKRD11 | c.7916T>A (p.Leu2639Gln) c.*7719T>A (n.*7719T>A) c.1190T>A (p.Leu397Gln) c.597T>A c.7814T>A (p.Leu2605Gln) c.7619T>A (p.Leu2540Gln) c.7787T>A (p.Leu2596Gln) | gnomAD v4 |
| 16 | g.89268555G>A | CA497165609 | ANKRD11 | c.7915C>T (p.Leu2639=) c.*7718C>T (n.*7718C>T) c.1189C>T (p.Leu397=) c.596C>T c.7813C>T (p.Leu2605=) c.7618C>T (p.Leu2540=) c.7786C>T (p.Leu2596=) | |
| 16 | g.89268555G>C | CA397145060 | ANKRD11 | c.7915C>G (p.Leu2639Val) c.*7718C>G (n.*7718C>G) c.1189C>G (p.Leu397Val) c.596C>G c.7813C>G (p.Leu2605Val) c.7618C>G (p.Leu2540Val) c.7786C>G (p.Leu2596Val) | |
| 16 | g.89268555G>T | CA397145061 | ANKRD11 | c.7915C>A (p.Leu2639Met) c.*7718C>A (n.*7718C>A) c.1189C>A (p.Leu397Met) c.596C>A c.7813C>A (p.Leu2605Met) c.7618C>A (p.Leu2540Met) c.7786C>A (p.Leu2596Met) | |
| 16 | g.89268556G>A | CA497165613 | ANKRD11 | c.7914C>T (p.Ser2638=) c.*7717C>T (n.*7717C>T) c.1188C>T (p.Ser396=) c.595C>T c.7812C>T (p.Ser2604=) c.7617C>T (p.Ser2539=) c.7785C>T (p.Ser2595=) | gnomAD v4 |
| 16 | g.89268556G>C | CA497165614 | ANKRD11 | c.7914C>G (p.Ser2638=) c.*7717C>G (n.*7717C>G) c.1188C>G (p.Ser396=) c.595C>G c.7812C>G (p.Ser2604=) c.7617C>G (p.Ser2539=) c.7785C>G (p.Ser2595=) | |
| 16 | g.89268556G>T | CA497165615 | ANKRD11 | c.7914C>A (p.Ser2638=) c.*7717C>A (n.*7717C>A) c.1188C>A (p.Ser396=) c.595C>A c.7812C>A (p.Ser2604=) c.7617C>A (p.Ser2539=) c.7785C>A (p.Ser2595=) | gnomAD v4 |
| 16 | g.89268557G>A | CA397145062 | ANKRD11 | c.7913C>T (p.Ser2638Phe) c.*7716C>T (n.*7716C>T) c.1187C>T (p.Ser396Phe) c.594C>T c.7811C>T (p.Ser2604Phe) c.7616C>T (p.Ser2539Phe) c.7784C>T (p.Ser2595Phe) | dbSNP gnomAD v4 |
| 16 | g.89268557G>C | CA397145063 | ANKRD11 | c.7913C>G (p.Ser2638Cys) c.*7716C>G (n.*7716C>G) c.1187C>G (p.Ser396Cys) c.594C>G c.7811C>G (p.Ser2604Cys) c.7616C>G (p.Ser2539Cys) c.7784C>G (p.Ser2595Cys) | |
| 16 | g.89268557G= | CA2241594788 | ANKRD11 | c.7913C= (p.Ser2638=) c.*7716C= (n.*7716C=) c.1187C= (p.Ser396=) c.594C= c.7811C= (p.Ser2604=) c.7616C= (p.Ser2539=) c.7784C= (p.Ser2595=) | |
| 16 | g.89268557G>T | CA397145064 | ANKRD11 | c.7913C>A (p.Ser2638Tyr) c.*7716C>A (n.*7716C>A) c.1187C>A (p.Ser396Tyr) c.594C>A c.7811C>A (p.Ser2604Tyr) c.7616C>A (p.Ser2539Tyr) c.7784C>A (p.Ser2595Tyr) | dbSNP gnomAD v4 |
| 16 | g.89268558A= | CA2241594789 | ANKRD11 | c.7912T= (p.Ser2638=) c.*7715T= (n.*7715T=) c.1186T= (p.Ser396=) c.593T= c.7810T= (p.Ser2604=) c.7615T= (p.Ser2539=) c.7783T= (p.Ser2595=) | |
| 16 | g.89268558A>C | CA397145065 | ANKRD11 | c.7912T>G (p.Ser2638Ala) c.*7715T>G (n.*7715T>G) c.1186T>G (p.Ser396Ala) c.593T>G c.7810T>G (p.Ser2604Ala) c.7615T>G (p.Ser2539Ala) c.7783T>G (p.Ser2595Ala) | |
| 16 | g.89268558A>G | CA397145066 | ANKRD11 | c.7912T>C (p.Ser2638Pro) c.*7715T>C (n.*7715T>C) c.1186T>C (p.Ser396Pro) c.593T>C c.7810T>C (p.Ser2604Pro) c.7615T>C (p.Ser2539Pro) c.7783T>C (p.Ser2595Pro) | |
| 16 | g.89268558A>T | CA286503920 | ANKRD11 | c.7912T>A (p.Ser2638Thr) c.*7715T>A (n.*7715T>A) c.1186T>A (p.Ser396Thr) c.593T>A c.7810T>A (p.Ser2604Thr) c.7615T>A (p.Ser2539Thr) c.7783T>A (p.Ser2595Thr) | dbSNP gnomAD v3 gnomAD v4 |
| 16 | g.89268559C>A | CA397145068 | ANKRD11 | c.7911G>T (p.Lys2637Asn) c.*7714G>T (n.*7714G>T) c.1185G>T (p.Lys395Asn) c.592G>T c.7809G>T (p.Lys2603Asn) c.7614G>T (p.Lys2538Asn) c.7782G>T (p.Lys2594Asn) | dbSNP |
| 16 | g.89268559C= | CA2241594790 | ANKRD11 | c.7911G= (p.Lys2637=) c.*7714G= (n.*7714G=) c.1185G= (p.Lys395=) c.592G= c.7809G= (p.Lys2603=) c.7614G= (p.Lys2538=) c.7782G= (p.Lys2594=) | |
| 16 | g.89268559C>G | CA397145067 | ANKRD11 | c.7911G>C (p.Lys2637Asn) c.*7714G>C (n.*7714G>C) c.1185G>C (p.Lys395Asn) c.592G>C c.7809G>C (p.Lys2603Asn) c.7614G>C (p.Lys2538Asn) c.7782G>C (p.Lys2594Asn) | |
| 16 | g.89268559C>T | CA497165619 | ANKRD11 | c.7911G>A (p.Lys2637=) c.*7714G>A (n.*7714G>A) c.1185G>A (p.Lys395=) c.592G>A c.7809G>A (p.Lys2603=) c.7614G>A (p.Lys2538=) c.7782G>A (p.Lys2594=) | gnomAD v4 |
| 16 | g.89268560T>A | CA397145069 | ANKRD11 | c.7910A>T (p.Lys2637Met) c.*7713A>T (n.*7713A>T) c.1184A>T (p.Lys395Met) c.591A>T c.7808A>T (p.Lys2603Met) c.7613A>T (p.Lys2538Met) c.7781A>T (p.Lys2594Met) |