UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
| 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) | |
| 16 | g.89268560T>C | CA397145070 | ANKRD11 | c.7910A>G (p.Lys2637Arg) c.*7713A>G (n.*7713A>G) c.1184A>G (p.Lys395Arg) c.591A>G c.7808A>G (p.Lys2603Arg) c.7613A>G (p.Lys2538Arg) c.7781A>G (p.Lys2594Arg) | |
| 16 | g.89268560T>G | CA397145071 | ANKRD11 | c.7910A>C (p.Lys2637Thr) c.*7713A>C (n.*7713A>C) c.1184A>C (p.Lys395Thr) c.591A>C c.7808A>C (p.Lys2603Thr) c.7613A>C (p.Lys2538Thr) c.7781A>C (p.Lys2594Thr) | |
| 16 | g.89268561T>A | CA397145072 | ANKRD11 | c.7909A>T (p.Lys2637Ter) c.*7712A>T (n.*7712A>T) c.1183A>T (p.Lys395Ter) c.590A>T c.7807A>T (p.Lys2603Ter) c.7612A>T (p.Lys2538Ter) c.7780A>T (p.Lys2594Ter) | |
| 16 | g.89268561T>C | CA397145073 | ANKRD11 | c.7909A>G (p.Lys2637Glu) c.*7712A>G (n.*7712A>G) c.1183A>G (p.Lys395Glu) c.590A>G c.7807A>G (p.Lys2603Glu) c.7612A>G (p.Lys2538Glu) c.7780A>G (p.Lys2594Glu) | |
| 16 | g.89268561T>G | CA397145074 | ANKRD11 | c.7909A>C (p.Lys2637Gln) c.*7712A>C (n.*7712A>C) c.1183A>C (p.Lys395Gln) c.590A>C c.7807A>C (p.Lys2603Gln) c.7612A>C (p.Lys2538Gln) c.7780A>C (p.Lys2594Gln) | |
| 16 | g.89268562G>A | CA497165621 | ANKRD11 | c.7908C>T (p.His2636=) c.*7711C>T (n.*7711C>T) c.1182C>T (p.His394=) c.589C>T c.7806C>T (p.His2602=) c.7611C>T (p.His2537=) c.7779C>T (p.His2593=) | dbSNP gnomAD v3 gnomAD v4 |
| 16 | g.89268562G>C | CA397145075 | ANKRD11 | c.7908C>G (p.His2636Gln) c.*7711C>G (n.*7711C>G) c.1182C>G (p.His394Gln) c.589C>G c.7806C>G (p.His2602Gln) c.7611C>G (p.His2537Gln) c.7779C>G (p.His2593Gln) | gnomAD v4 |
| 16 | g.89268562G= | CA2241594791 | ANKRD11 | c.7908C= (p.His2636=) c.*7711C= (n.*7711C=) c.1182C= (p.His394=) c.589C= c.7806C= (p.His2602=) c.7611C= (p.His2537=) c.7779C= (p.His2593=) | |
| 16 | g.89268562G>T | CA397145076 | ANKRD11 | c.7908C>A (p.His2636Gln) c.*7711C>A (n.*7711C>A) c.1182C>A (p.His394Gln) c.589C>A c.7806C>A (p.His2602Gln) c.7611C>A (p.His2537Gln) c.7779C>A (p.His2593Gln) | |
| 16 | g.89268563T>A | CA397145077 | ANKRD11 | c.7907A>T (p.His2636Leu) c.*7710A>T (n.*7710A>T) c.1181A>T (p.His394Leu) c.588A>T c.7805A>T (p.His2602Leu) c.7610A>T (p.His2537Leu) c.7778A>T (p.His2593Leu) | |
| 16 | g.89268563T>C | CA397145078 | ANKRD11 | c.7907A>G (p.His2636Arg) c.*7710A>G (n.*7710A>G) c.1181A>G (p.His394Arg) c.588A>G c.7805A>G (p.His2602Arg) c.7610A>G (p.His2537Arg) c.7778A>G (p.His2593Arg) | |
| 16 | g.89268563T>G | CA397145079 | ANKRD11 | c.7907A>C (p.His2636Pro) c.*7710A>C (n.*7710A>C) c.1181A>C (p.His394Pro) c.588A>C c.7805A>C (p.His2602Pro) c.7610A>C (p.His2537Pro) c.7778A>C (p.His2593Pro) | gnomAD v4 |
| 16 | g.89268564G>A | CA397145082 | ANKRD11 | c.7906C>T (p.His2636Tyr) c.*7709C>T (n.*7709C>T) c.1180C>T (p.His394Tyr) c.587C>T c.7804C>T (p.His2602Tyr) c.7609C>T (p.His2537Tyr) c.7777C>T (p.His2593Tyr) | gnomAD v4 COSMIC |
| 16 | g.89268564G>C | CA397145081 | ANKRD11 | c.7906C>G (p.His2636Asp) c.*7709C>G (n.*7709C>G) c.1180C>G (p.His394Asp) c.587C>G c.7804C>G (p.His2602Asp) c.7609C>G (p.His2537Asp) c.7777C>G (p.His2593Asp) | |
| 16 | g.89268564G>T | CA397145080 | ANKRD11 | c.7906C>A (p.His2636Asn) c.*7709C>A (n.*7709C>A) c.1180C>A (p.His394Asn) c.587C>A c.7804C>A (p.His2602Asn) c.7609C>A (p.His2537Asn) c.7777C>A (p.His2593Asn) | gnomAD v4 |
| 16 | g.89268565C>A | CA497165623 | ANKRD11 | c.7905G>T (p.Gly2635=) c.*7708G>T (n.*7708G>T) c.1179G>T (p.Gly393=) c.586G>T c.7803G>T (p.Gly2601=) c.7608G>T (p.Gly2536=) c.7776G>T (p.Gly2592=) | |
| 16 | g.89268565C= | CA2241594792 | ANKRD11 | c.7905G= (p.Gly2635=) c.*7708G= (n.*7708G=) c.1179G= (p.Gly393=) c.586G= c.7803G= (p.Gly2601=) c.7608G= (p.Gly2536=) c.7776G= (p.Gly2592=) | |
| 16 | g.89268565C>G | CA497165624 | ANKRD11 | c.7905G>C (p.Gly2635=) c.*7708G>C (n.*7708G>C) c.1179G>C (p.Gly393=) c.586G>C c.7803G>C (p.Gly2601=) c.7608G>C (p.Gly2536=) c.7776G>C (p.Gly2592=) | dbSNP gnomAD v3 gnomAD v4 |
| 16 | g.89268565C>T | CA497165625 | ANKRD11 | c.7905G>A (p.Gly2635=) c.*7708G>A (n.*7708G>A) c.1179G>A (p.Gly393=) c.586G>A c.7803G>A (p.Gly2601=) c.7608G>A (p.Gly2536=) c.7776G>A (p.Gly2592=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.89268566C>A | CA397145083 | ANKRD11 | c.7904G>T (p.Gly2635Val) c.*7707G>T (n.*7707G>T) c.1178G>T (p.Gly393Val) c.585G>T c.7802G>T (p.Gly2601Val) c.7607G>T (p.Gly2536Val) c.7775G>T (p.Gly2592Val) | |
| 16 | g.89268566C>G | CA397145084 | ANKRD11 | c.7904G>C (p.Gly2635Ala) c.*7707G>C (n.*7707G>C) c.1178G>C (p.Gly393Ala) c.585G>C c.7802G>C (p.Gly2601Ala) c.7607G>C (p.Gly2536Ala) c.7775G>C (p.Gly2592Ala) | |
| 16 | g.89268566C>T | CA397145085 | ANKRD11 | c.7904G>A (p.Gly2635Glu) c.*7707G>A (n.*7707G>A) c.1178G>A (p.Gly393Glu) c.585G>A c.7802G>A (p.Gly2601Glu) c.7607G>A (p.Gly2536Glu) c.7775G>A (p.Gly2592Glu) | |
| 16 | g.89268567C>A | CA397145086 | ANKRD11 | c.7903G>T (p.Gly2635Trp) c.*7706G>T (n.*7706G>T) c.1177G>T (p.Gly393Trp) c.584G>T c.7801G>T (p.Gly2601Trp) c.7606G>T (p.Gly2536Trp) c.7774G>T (p.Gly2592Trp) | gnomAD v4 |
| 16 | g.89268567C>G | CA397145087 | ANKRD11 | c.7903G>C (p.Gly2635Arg) c.*7706G>C (n.*7706G>C) c.1177G>C (p.Gly393Arg) c.584G>C c.7801G>C (p.Gly2601Arg) c.7606G>C (p.Gly2536Arg) c.7774G>C (p.Gly2592Arg) | |
| 16 | g.89268567C>T | CA397145088 | ANKRD11 | c.7903G>A (p.Gly2635Arg) c.*7706G>A (n.*7706G>A) c.1177G>A (p.Gly393Arg) c.584G>A c.7801G>A (p.Gly2601Arg) c.7606G>A (p.Gly2536Arg) c.7774G>A (p.Gly2592Arg) | gnomAD v4 |
| 16 | g.89268568G>A | CA286503921 | ANKRD11 | c.7902C>T (p.Ala2634=) c.*7705C>T (n.*7705C>T) c.1176C>T (p.Ala392=) c.583C>T c.7800C>T (p.Ala2600=) c.7605C>T (p.Ala2535=) c.7773C>T (p.Ala2591=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.89268568G>C | CA497165629 | ANKRD11 | c.7902C>G (p.Ala2634=) c.*7705C>G (n.*7705C>G) c.1176C>G (p.Ala392=) c.583C>G c.7800C>G (p.Ala2600=) c.7605C>G (p.Ala2535=) c.7773C>G (p.Ala2591=) | gnomAD v4 |
| 16 | g.89268568G= | CA2241594793 | ANKRD11 | c.7902C= (p.Ala2634=) c.*7705C= (n.*7705C=) c.1176C= (p.Ala392=) c.583C= c.7800C= (p.Ala2600=) c.7605C= (p.Ala2535=) c.7773C= (p.Ala2591=) | |
| 16 | g.89268568G>T | CA497165631 | ANKRD11 | c.7902C>A (p.Ala2634=) c.*7705C>A (n.*7705C>A) c.1176C>A (p.Ala392=) c.583C>A c.7800C>A (p.Ala2600=) c.7605C>A (p.Ala2535=) c.7773C>A (p.Ala2591=) | gnomAD v4 |
| 16 | g.89268569G>A | CA397145089 | ANKRD11 | c.7901C>T (p.Ala2634Val) c.*7704C>T (n.*7704C>T) c.1175C>T (p.Ala392Val) c.582C>T c.7799C>T (p.Ala2600Val) c.7604C>T (p.Ala2535Val) c.7772C>T (p.Ala2591Val) | |
| 16 | g.89268569G>C | CA397145090 | ANKRD11 | c.7901C>G (p.Ala2634Gly) c.*7704C>G (n.*7704C>G) c.1175C>G (p.Ala392Gly) c.582C>G c.7799C>G (p.Ala2600Gly) c.7604C>G (p.Ala2535Gly) c.7772C>G (p.Ala2591Gly) | |
| 16 | g.89268569G>T | CA397145091 | ANKRD11 | c.7901C>A (p.Ala2634Asp) c.*7704C>A (n.*7704C>A) c.1175C>A (p.Ala392Asp) c.582C>A c.7799C>A (p.Ala2600Asp) c.7604C>A (p.Ala2535Asp) c.7772C>A (p.Ala2591Asp) | |
| 16 | g.89268570C>A | CA397145092 | ANKRD11 | c.7900G>T (p.Ala2634Ser) c.*7703G>T (n.*7703G>T) c.1174G>T (p.Ala392Ser) c.581G>T c.7798G>T (p.Ala2600Ser) c.7603G>T (p.Ala2535Ser) c.7771G>T (p.Ala2591Ser) | |
| 16 | g.89268570C= | CA2241594794 | ANKRD11 | c.7900G= (p.Ala2634=) c.*7703G= (n.*7703G=) c.1174G= (p.Ala392=) c.581G= c.7798G= (p.Ala2600=) c.7603G= (p.Ala2535=) c.7771G= (p.Ala2591=) | |
| 16 | g.89268570C>G | CA397145093 | ANKRD11 | c.7900G>C (p.Ala2634Pro) c.*7703G>C (n.*7703G>C) c.1174G>C (p.Ala392Pro) c.581G>C c.7798G>C (p.Ala2600Pro) c.7603G>C (p.Ala2535Pro) c.7771G>C (p.Ala2591Pro) | |
| 16 | g.89268570C>T | CA397145094 | ANKRD11 | c.7900G>A (p.Ala2634Thr) c.*7703G>A (n.*7703G>A) c.1174G>A (p.Ala392Thr) c.581G>A c.7798G>A (p.Ala2600Thr) c.7603G>A (p.Ala2535Thr) c.7771G>A (p.Ala2591Thr) | dbSNP gnomAD v4 |
| 16 | g.89268571G>A | CA8240975 | ANKRD11 | c.7899C>T (p.Pro2633=) c.*7702C>T (n.*7702C>T) c.1173C>T (p.Pro391=) c.580C>T c.7797C>T (p.Pro2599=) c.7602C>T (p.Pro2534=) c.7770C>T (p.Pro2590=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.89268571G>C | CA497165634 | ANKRD11 | c.7899C>G (p.Pro2633=) c.*7702C>G (n.*7702C>G) c.1173C>G (p.Pro391=) c.580C>G c.7797C>G (p.Pro2599=) c.7602C>G (p.Pro2534=) c.7770C>G (p.Pro2590=) | gnomAD v4 |
| 16 | g.89268571G= | CA2241594795 | ANKRD11 | c.7899C= (p.Pro2633=) c.*7702C= (n.*7702C=) c.1173C= (p.Pro391=) c.580C= c.7797C= (p.Pro2599=) c.7602C= (p.Pro2534=) c.7770C= (p.Pro2590=) | |
| 16 | g.89268571G>T | CA497165632 | ANKRD11 | c.7899C>A (p.Pro2633=) c.*7702C>A (n.*7702C>A) c.1173C>A (p.Pro391=) c.580C>A c.7797C>A (p.Pro2599=) c.7602C>A (p.Pro2534=) c.7770C>A (p.Pro2590=) | gnomAD v4 |
| 16 | g.89268572G>A | CA397145095 | ANKRD11 | c.7898C>T (p.Pro2633Leu) c.*7701C>T (n.*7701C>T) c.1172C>T (p.Pro391Leu) c.579C>T c.7796C>T (p.Pro2599Leu) c.7601C>T (p.Pro2534Leu) c.7769C>T (p.Pro2590Leu) | gnomAD v4 |
| 16 | g.89268572G>C | CA397145097 | ANKRD11 | c.7898C>G (p.Pro2633Arg) c.*7701C>G (n.*7701C>G) c.1172C>G (p.Pro391Arg) c.579C>G c.7796C>G (p.Pro2599Arg) c.7601C>G (p.Pro2534Arg) c.7769C>G (p.Pro2590Arg) | |
| 16 | g.89268572G>T | CA397145096 | ANKRD11 | c.7898C>A (p.Pro2633His) c.*7701C>A (n.*7701C>A) c.1172C>A (p.Pro391His) c.579C>A c.7796C>A (p.Pro2599His) c.7601C>A (p.Pro2534His) c.7769C>A (p.Pro2590His) | gnomAD v4 |
| 16 | g.89268573G>A | CA397145098 | ANKRD11 | c.7897C>T (p.Pro2633Ser) c.*7700C>T (n.*7700C>T) c.1171C>T (p.Pro391Ser) c.578C>T c.7795C>T (p.Pro2599Ser) c.7600C>T (p.Pro2534Ser) c.7768C>T (p.Pro2590Ser) | |
| 16 | g.89268573G>C | CA286503923 | ANKRD11 | c.7897C>G (p.Pro2633Ala) c.*7700C>G (n.*7700C>G) c.1171C>G (p.Pro391Ala) c.578C>G c.7795C>G (p.Pro2599Ala) c.7600C>G (p.Pro2534Ala) c.7768C>G (p.Pro2590Ala) | dbSNP |
| 16 | g.89268573G= | CA2241594796 | ANKRD11 | c.7897C= (p.Pro2633=) c.*7700C= (n.*7700C=) c.1171C= (p.Pro391=) c.578C= c.7795C= (p.Pro2599=) c.7600C= (p.Pro2534=) c.7768C= (p.Pro2590=) | |
| 16 | g.89268573G>T | CA397145099 | ANKRD11 | c.7897C>A (p.Pro2633Thr) c.*7700C>A (n.*7700C>A) c.1171C>A (p.Pro391Thr) c.578C>A c.7795C>A (p.Pro2599Thr) c.7600C>A (p.Pro2534Thr) c.7768C>A (p.Pro2590Thr) | |
| 16 | g.89268574G>A | CA497165636 | ANKRD11 | c.7896C>T (p.Asp2632=) c.*7699C>T (n.*7699C>T) c.1170C>T (p.Asp390=) c.577C>T c.7794C>T (p.Asp2598=) c.7599C>T (p.Asp2533=) c.7767C>T (p.Asp2589=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.89268574G>C | CA397145100 | ANKRD11 | c.7896C>G (p.Asp2632Glu) c.*7699C>G (n.*7699C>G) c.1170C>G (p.Asp390Glu) c.577C>G c.7794C>G (p.Asp2598Glu) c.7599C>G (p.Asp2533Glu) c.7767C>G (p.Asp2589Glu) | |
| 16 | g.89268574G= | CA2241594797 | ANKRD11 | c.7896C= (p.Asp2632=) c.*7699C= (n.*7699C=) c.1170C= (p.Asp390=) c.577C= c.7794C= (p.Asp2598=) c.7599C= (p.Asp2533=) c.7767C= (p.Asp2589=) | |
| 16 | g.89268574G>T | CA397145101 | ANKRD11 | c.7896C>A (p.Asp2632Glu) c.*7699C>A (n.*7699C>A) c.1170C>A (p.Asp390Glu) c.577C>A c.7794C>A (p.Asp2598Glu) c.7599C>A (p.Asp2533Glu) c.7767C>A (p.Asp2589Glu) | dbSNP |
| 16 | g.89268575T>A | CA397145102 | ANKRD11 | c.7895A>T (p.Asp2632Val) c.*7698A>T (n.*7698A>T) c.1169A>T (p.Asp390Val) c.576A>T c.7793A>T (p.Asp2598Val) c.7598A>T (p.Asp2533Val) c.7766A>T (p.Asp2589Val) | |
| 16 | g.89268575T>C | CA397145103 | ANKRD11 | c.7895A>G (p.Asp2632Gly) c.*7698A>G (n.*7698A>G) c.1169A>G (p.Asp390Gly) c.576A>G c.7793A>G (p.Asp2598Gly) c.7598A>G (p.Asp2533Gly) c.7766A>G (p.Asp2589Gly) | |
| 16 | g.89268575T>G | CA397145104 | ANKRD11 | c.7895A>C (p.Asp2632Ala) c.*7698A>C (n.*7698A>C) c.1169A>C (p.Asp390Ala) c.576A>C c.7793A>C (p.Asp2598Ala) c.7598A>C (p.Asp2533Ala) c.7766A>C (p.Asp2589Ala) | |
| 16 | g.89268576C>A | CA397145105 | ANKRD11 | c.7894G>T (p.Asp2632Tyr) c.*7697G>T (n.*7697G>T) c.1168G>T (p.Asp390Tyr) c.575G>T c.7792G>T (p.Asp2598Tyr) c.7597G>T (p.Asp2533Tyr) c.7765G>T (p.Asp2589Tyr) | |
| 16 | g.89268576C>G | CA397145106 | ANKRD11 | c.7894G>C (p.Asp2632His) c.*7697G>C (n.*7697G>C) c.1168G>C (p.Asp390His) c.575G>C c.7792G>C (p.Asp2598His) c.7597G>C (p.Asp2533His) c.7765G>C (p.Asp2589His) | |
| 16 | g.89268576C>T | CA397145107 | ANKRD11 | c.7894G>A (p.Asp2632Asn) c.*7697G>A (n.*7697G>A) c.1168G>A (p.Asp390Asn) c.575G>A c.7792G>A (p.Asp2598Asn) c.7597G>A (p.Asp2533Asn) c.7765G>A (p.Asp2589Asn) | |
| 16 | g.89268577C>A | CA497165637 | ANKRD11 | c.7893G>T (p.Leu2631=) c.*7696G>T (n.*7696G>T) c.1167G>T (p.Leu389=) c.574G>T c.7791G>T (p.Leu2597=) c.7596G>T (p.Leu2532=) c.7764G>T (p.Leu2588=) | |
| 16 | g.89268577C= | CA2241594798 | ANKRD11 | c.7893G= (p.Leu2631=) c.*7696G= (n.*7696G=) c.1167G= (p.Leu389=) c.574G= c.7791G= (p.Leu2597=) c.7596G= (p.Leu2532=) c.7764G= (p.Leu2588=) | |
| 16 | g.89268577C>G | CA497165639 | ANKRD11 | c.7893G>C (p.Leu2631=) c.*7696G>C (n.*7696G>C) c.1167G>C (p.Leu389=) c.574G>C c.7791G>C (p.Leu2597=) c.7596G>C (p.Leu2532=) c.7764G>C (p.Leu2588=) | |
| 16 | g.89268577C>T | CA497165638 | ANKRD11 | c.7893G>A (p.Leu2631=) c.*7696G>A (n.*7696G>A) c.1167G>A (p.Leu389=) c.574G>A c.7791G>A (p.Leu2597=) c.7596G>A (p.Leu2532=) c.7764G>A (p.Leu2588=) | dbSNP gnomAD v2 |
| 16 | g.89268578A>C | CA397145109 | ANKRD11 | c.7892T>G (p.Leu2631Arg) c.*7695T>G (n.*7695T>G) c.1166T>G (p.Leu389Arg) c.573T>G c.7790T>G (p.Leu2597Arg) c.7595T>G (p.Leu2532Arg) c.7763T>G (p.Leu2588Arg) | |
| 16 | g.89268578A>G | CA397145110 | ANKRD11 | c.7892T>C (p.Leu2631Pro) c.*7695T>C (n.*7695T>C) c.1166T>C (p.Leu389Pro) c.573T>C c.7790T>C (p.Leu2597Pro) c.7595T>C (p.Leu2532Pro) c.7763T>C (p.Leu2588Pro) | |
| 16 | g.89268578A>T | CA397145108 | ANKRD11 | c.7892T>A (p.Leu2631Gln) c.*7695T>A (n.*7695T>A) c.1166T>A (p.Leu389Gln) c.573T>A c.7790T>A (p.Leu2597Gln) c.7595T>A (p.Leu2532Gln) c.7763T>A (p.Leu2588Gln) | |
| 16 | g.89268579G>A | CA8240976 | ANKRD11 | c.7891C>T (p.Leu2631=) c.*7694C>T (n.*7694C>T) c.1165C>T (p.Leu389=) c.572C>T c.7789C>T (p.Leu2597=) c.7594C>T (p.Leu2532=) c.7762C>T (p.Leu2588=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.89268579G>C | CA397145111 | ANKRD11 | c.7891C>G (p.Leu2631Val) c.*7694C>G (n.*7694C>G) c.1165C>G (p.Leu389Val) c.572C>G c.7789C>G (p.Leu2597Val) c.7594C>G (p.Leu2532Val) c.7762C>G (p.Leu2588Val) | |
| 16 | g.89268579G= | CA2241594799 | ANKRD11 | c.7891C= (p.Leu2631=) c.*7694C= (n.*7694C=) c.1165C= (p.Leu389=) c.572C= c.7789C= (p.Leu2597=) c.7594C= (p.Leu2532=) c.7762C= (p.Leu2588=) | |
| 16 | g.89268579G>T | CA397145112 | ANKRD11 | c.7891C>A (p.Leu2631Met) c.*7694C>A (n.*7694C>A) c.1165C>A (p.Leu389Met) c.572C>A c.7789C>A (p.Leu2597Met) c.7594C>A (p.Leu2532Met) c.7762C>A (p.Leu2588Met) | gnomAD v4 |
| 16 | g.89268580T>A | CA397145113 | ANKRD11 | c.7890A>T (p.Glu2630Asp) c.*7693A>T (n.*7693A>T) c.1164A>T (p.Glu388Asp) c.571A>T c.7788A>T (p.Glu2596Asp) c.7593A>T (p.Glu2531Asp) c.7761A>T (p.Glu2587Asp) | gnomAD v4 |
| 16 | g.89268580T>C | CA497165644 | ANKRD11 | c.7890A>G (p.Glu2630=) c.*7693A>G (n.*7693A>G) c.1164A>G (p.Glu388=) c.571A>G c.7788A>G (p.Glu2596=) c.7593A>G (p.Glu2531=) c.7761A>G (p.Glu2587=) | |
| 16 | g.89268580T>G | CA397145114 | ANKRD11 | c.7890A>C (p.Glu2630Asp) c.*7693A>C (n.*7693A>C) c.1164A>C (p.Glu388Asp) c.571A>C c.7788A>C (p.Glu2596Asp) c.7593A>C (p.Glu2531Asp) c.7761A>C (p.Glu2587Asp) | |
| 16 | g.89268581T>A | CA397145115 | ANKRD11 | c.7889A>T (p.Glu2630Val) c.*7692A>T (n.*7692A>T) c.1163A>T (p.Glu388Val) c.570A>T c.7787A>T (p.Glu2596Val) c.7592A>T (p.Glu2531Val) c.7760A>T (p.Glu2587Val) | |
| 16 | g.89268581T>C | CA397145116 | ANKRD11 | c.7889A>G (p.Glu2630Gly) c.*7692A>G (n.*7692A>G) c.1163A>G (p.Glu388Gly) c.570A>G c.7787A>G (p.Glu2596Gly) c.7592A>G (p.Glu2531Gly) c.7760A>G (p.Glu2587Gly) | |
| 16 | g.89268581T>G | CA397145117 | ANKRD11 | c.7889A>C (p.Glu2630Ala) c.*7692A>C (n.*7692A>C) c.1163A>C (p.Glu388Ala) c.570A>C c.7787A>C (p.Glu2596Ala) c.7592A>C (p.Glu2531Ala) c.7760A>C (p.Glu2587Ala) | |
| 16 | g.89268582C>A | CA397145118 | ANKRD11 | c.7888G>T (p.Glu2630Ter) c.*7691G>T (n.*7691G>T) c.1162G>T (p.Glu388Ter) c.569G>T c.7786G>T (p.Glu2596Ter) c.7591G>T (p.Glu2531Ter) c.7759G>T (p.Glu2587Ter) | |
| 16 | g.89268582C>G | CA397145119 | ANKRD11 | c.7888G>C (p.Glu2630Gln) c.*7691G>C (n.*7691G>C) c.1162G>C (p.Glu388Gln) c.569G>C c.7786G>C (p.Glu2596Gln) c.7591G>C (p.Glu2531Gln) c.7759G>C (p.Glu2587Gln) | |
| 16 | g.89268582C>T | CA397145120 | ANKRD11 | c.7888G>A (p.Glu2630Lys) c.*7691G>A (n.*7691G>A) c.1162G>A (p.Glu388Lys) c.569G>A c.7786G>A (p.Glu2596Lys) c.7591G>A (p.Glu2531Lys) c.7759G>A (p.Glu2587Lys) | |
| 16 | g.89268583_89268604dup | CA2573054292 | ANKRD11 | c.7867_7888dup (p.Glu2630GlyfsTer?) c.*7670_*7691dup (n.*7670_*7691dup) c.1141_1162dup (p.Glu388GlyfsTer?) c.548_569dup c.7765_7786dup (p.Glu2596GlyfsTer?) c.7570_7591dup (p.Glu2531GlyfsTer?) c.7738_7759dup (p.Glu2587GlyfsTer?) | ClinVar dbSNP |
| 16 | g.89268583C>A | CA397145121 | ANKRD11 | c.7887G>T (p.Gln2629His) c.*7690G>T (n.*7690G>T) c.1161G>T (p.Gln387His) c.568G>T c.7785G>T (p.Gln2595His) c.7590G>T (p.Gln2530His) c.7758G>T (p.Gln2586His) | |
| 16 | g.89268583C= | CA2241594800 | ANKRD11 | c.7887G= (p.Gln2629=) c.*7690G= (n.*7690G=) c.1161G= (p.Gln387=) c.568G= c.7785G= (p.Gln2595=) c.7590G= (p.Gln2530=) c.7758G= (p.Gln2586=) | |
| 16 | g.89268583C>G | CA397145122 | ANKRD11 | c.7887G>C (p.Gln2629His) c.*7690G>C (n.*7690G>C) c.1161G>C (p.Gln387His) c.568G>C c.7785G>C (p.Gln2595His) c.7590G>C (p.Gln2530His) c.7758G>C (p.Gln2586His) | |
| 16 | g.89268583C>T | CA8240977 | ANKRD11 | c.7887G>A (p.Gln2629=) c.*7690G>A (n.*7690G>A) c.1161G>A (p.Gln387=) c.568G>A c.7785G>A (p.Gln2595=) c.7590G>A (p.Gln2530=) c.7758G>A (p.Gln2586=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.89268584T>A | CA397145123 | ANKRD11 | c.7886A>T (p.Gln2629Leu) c.*7689A>T (n.*7689A>T) c.1160A>T (p.Gln387Leu) c.567A>T c.7784A>T (p.Gln2595Leu) c.7589A>T (p.Gln2530Leu) c.7757A>T (p.Gln2586Leu) | |
| 16 | g.89268584T>C | CA397145125 | ANKRD11 | c.7886A>G (p.Gln2629Arg) c.*7689A>G (n.*7689A>G) c.1160A>G (p.Gln387Arg) c.567A>G c.7784A>G (p.Gln2595Arg) c.7589A>G (p.Gln2530Arg) c.7757A>G (p.Gln2586Arg) | gnomAD v4 |
| 16 | g.89268584T>G | CA397145124 | ANKRD11 | c.7886A>C (p.Gln2629Pro) c.*7689A>C (n.*7689A>C) c.1160A>C (p.Gln387Pro) c.567A>C c.7784A>C (p.Gln2595Pro) c.7589A>C (p.Gln2530Pro) c.7757A>C (p.Gln2586Pro) | |
| 16 | g.89268585G>A | CA397145126 | ANKRD11 | c.7885C>T (p.Gln2629Ter) c.*7688C>T (n.*7688C>T) c.1159C>T (p.Gln387Ter) c.566C>T c.7783C>T (p.Gln2595Ter) c.7588C>T (p.Gln2530Ter) c.7756C>T (p.Gln2586Ter) | |
| 16 | g.89268585G>C | CA397145127 | ANKRD11 | c.7885C>G (p.Gln2629Glu) c.*7688C>G (n.*7688C>G) c.1159C>G (p.Gln387Glu) c.566C>G c.7783C>G (p.Gln2595Glu) c.7588C>G (p.Gln2530Glu) c.7756C>G (p.Gln2586Glu) | |
| 16 | g.89268585G>T | CA397145128 | ANKRD11 | c.7885C>A (p.Gln2629Lys) c.*7688C>A (n.*7688C>A) c.1159C>A (p.Gln387Lys) c.566C>A c.7783C>A (p.Gln2595Lys) c.7588C>A (p.Gln2530Lys) c.7756C>A (p.Gln2586Lys) | ClinVar gnomAD v4 |
| 16 | g.89268586C>A | CA497165649 | ANKRD11 | c.7884G>T (p.Val2628=) c.*7687G>T (n.*7687G>T) c.1158G>T (p.Val386=) c.565G>T c.7782G>T (p.Val2594=) c.7587G>T (p.Val2529=) c.7755G>T (p.Val2585=) | |
| 16 | g.89268586C>G | CA497165650 | ANKRD11 | c.7884G>C (p.Val2628=) c.*7687G>C (n.*7687G>C) c.1158G>C (p.Val386=) c.565G>C c.7782G>C (p.Val2594=) c.7587G>C (p.Val2529=) c.7755G>C (p.Val2585=) | |
| 16 | g.89268586C>T | CA497165651 | ANKRD11 | c.7884G>A (p.Val2628=) c.*7687G>A (n.*7687G>A) c.1158G>A (p.Val386=) c.565G>A c.7782G>A (p.Val2594=) c.7587G>A (p.Val2529=) c.7755G>A (p.Val2585=) | |
| 16 | g.89268587A>C | CA397145129 | ANKRD11 | c.7883T>G (p.Val2628Gly) c.*7686T>G (n.*7686T>G) c.1157T>G (p.Val386Gly) c.564T>G c.7781T>G (p.Val2594Gly) c.7586T>G (p.Val2529Gly) c.7754T>G (p.Val2585Gly) | |
| 16 | g.89268587A>G | CA397145130 | ANKRD11 | c.7883T>C (p.Val2628Ala) c.*7686T>C (n.*7686T>C) c.1157T>C (p.Val386Ala) c.564T>C c.7781T>C (p.Val2594Ala) c.7586T>C (p.Val2529Ala) c.7754T>C (p.Val2585Ala) | |
| 16 | g.89268587A>T | CA397145131 | ANKRD11 | c.7883T>A (p.Val2628Glu) c.*7686T>A (n.*7686T>A) c.1157T>A (p.Val386Glu) c.564T>A c.7781T>A (p.Val2594Glu) c.7586T>A (p.Val2529Glu) c.7754T>A (p.Val2585Glu) | |
| 16 | g.89268588C>A | CA397145132 | ANKRD11 | c.7882G>T (p.Val2628Leu) c.*7685G>T (n.*7685G>T) c.1156G>T (p.Val386Leu) c.563G>T c.7780G>T (p.Val2594Leu) c.7585G>T (p.Val2529Leu) c.7753G>T (p.Val2585Leu) | gnomAD v4 |
| 16 | g.89268588C= | CA2241594801 | ANKRD11 | c.7882G= (p.Val2628=) c.*7685G= (n.*7685G=) c.1156G= (p.Val386=) c.563G= c.7780G= (p.Val2594=) c.7585G= (p.Val2529=) c.7753G= (p.Val2585=) | |
| 16 | g.89268588C>G | CA397145133 | ANKRD11 | c.7882G>C (p.Val2628Leu) c.*7685G>C (n.*7685G>C) c.1156G>C (p.Val386Leu) c.563G>C c.7780G>C (p.Val2594Leu) c.7585G>C (p.Val2529Leu) c.7753G>C (p.Val2585Leu) | |
| 16 | g.89268588C>T | CA8240978 | ANKRD11 | c.7882G>A (p.Val2628Met) c.*7685G>A (n.*7685G>A) c.1156G>A (p.Val386Met) c.563G>A c.7780G>A (p.Val2594Met) c.7585G>A (p.Val2529Met) c.7753G>A (p.Val2585Met) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.89268589C>A | CA397145134 | ANKRD11 | c.7881G>T (p.Lys2627Asn) c.*7684G>T (n.*7684G>T) c.1155G>T (p.Lys385Asn) c.562G>T c.7779G>T (p.Lys2593Asn) c.7584G>T (p.Lys2528Asn) c.7752G>T (p.Lys2584Asn) | |
| 16 | g.89268589C>G | CA397145135 | ANKRD11 | c.7881G>C (p.Lys2627Asn) c.*7684G>C (n.*7684G>C) c.1155G>C (p.Lys385Asn) c.562G>C c.7779G>C (p.Lys2593Asn) c.7584G>C (p.Lys2528Asn) c.7752G>C (p.Lys2584Asn) | |
| 16 | g.89268589C>T | CA497165654 | ANKRD11 | c.7881G>A (p.Lys2627=) c.*7684G>A (n.*7684G>A) c.1155G>A (p.Lys385=) c.562G>A c.7779G>A (p.Lys2593=) c.7584G>A (p.Lys2528=) c.7752G>A (p.Lys2584=) | ClinVar gnomAD v4 |
| 16 | g.89268590T>A | CA397145137 | ANKRD11 | c.7880A>T (p.Lys2627Met) c.*7683A>T (n.*7683A>T) c.1154A>T (p.Lys385Met) c.561A>T c.7778A>T (p.Lys2593Met) c.7583A>T (p.Lys2528Met) c.7751A>T (p.Lys2584Met) | |
| 16 | g.89268590T>C | CA8240979 | ANKRD11 | c.7880A>G (p.Lys2627Arg) c.*7683A>G (n.*7683A>G) c.1154A>G (p.Lys385Arg) c.561A>G c.7778A>G (p.Lys2593Arg) c.7583A>G (p.Lys2528Arg) c.7751A>G (p.Lys2584Arg) | dbSNP ExAC gnomAD v4 |
| 16 | g.89268590T>G | CA397145136 | ANKRD11 | c.7880A>C (p.Lys2627Thr) c.*7683A>C (n.*7683A>C) c.1154A>C (p.Lys385Thr) c.561A>C c.7778A>C (p.Lys2593Thr) c.7583A>C (p.Lys2528Thr) c.7751A>C (p.Lys2584Thr) | |
| 16 | g.89268590T= | CA2241594802 | ANKRD11 | c.7880A= (p.Lys2627=) c.*7683A= (n.*7683A=) c.1154A= (p.Lys385=) c.561A= c.7778A= (p.Lys2593=) c.7583A= (p.Lys2528=) c.7751A= (p.Lys2584=) | |
| 16 | g.89268591T>A | CA397145138 | ANKRD11 | c.7879A>T (p.Lys2627Ter) c.*7682A>T (n.*7682A>T) c.1153A>T (p.Lys385Ter) c.560A>T c.7777A>T (p.Lys2593Ter) c.7582A>T (p.Lys2528Ter) c.7750A>T (p.Lys2584Ter) | |
| 16 | g.89268591T>C | CA286503926 | ANKRD11 | c.7879A>G (p.Lys2627Glu) c.*7682A>G (n.*7682A>G) c.1153A>G (p.Lys385Glu) c.560A>G c.7777A>G (p.Lys2593Glu) c.7582A>G (p.Lys2528Glu) c.7750A>G (p.Lys2584Glu) | dbSNP |
| 16 | g.89268591T>G | CA397145139 | ANKRD11 | c.7879A>C (p.Lys2627Gln) c.*7682A>C (n.*7682A>C) c.1153A>C (p.Lys385Gln) c.560A>C c.7777A>C (p.Lys2593Gln) c.7582A>C (p.Lys2528Gln) c.7750A>C (p.Lys2584Gln) | |
| 16 | g.89268591T= | CA2241594803 | ANKRD11 | c.7879A= (p.Lys2627=) c.*7682A= (n.*7682A=) c.1153A= (p.Lys385=) c.560A= c.7777A= (p.Lys2593=) c.7582A= (p.Lys2528=) c.7750A= (p.Lys2584=) | |
| 16 | g.89268592C>A | CA497165660 | ANKRD11 | c.7878G>T (p.Leu2626=) c.*7681G>T (n.*7681G>T) c.1152G>T (p.Leu384=) c.559G>T c.7776G>T (p.Leu2592=) c.7581G>T (p.Leu2527=) c.7749G>T (p.Leu2583=) | |
| 16 | g.89268592C>G | CA497165658 | ANKRD11 | c.7878G>C (p.Leu2626=) c.*7681G>C (n.*7681G>C) c.1152G>C (p.Leu384=) c.559G>C c.7776G>C (p.Leu2592=) c.7581G>C (p.Leu2527=) c.7749G>C (p.Leu2583=) | |
| 16 | g.89268592C>T | CA497165657 | ANKRD11 | c.7878G>A (p.Leu2626=) c.*7681G>A (n.*7681G>A) c.1152G>A (p.Leu384=) c.559G>A c.7776G>A (p.Leu2592=) c.7581G>A (p.Leu2527=) c.7749G>A (p.Leu2583=) | |
| 16 | g.89268593A>C | CA397145140 | ANKRD11 | c.7877T>G (p.Leu2626Arg) c.*7680T>G (n.*7680T>G) c.1151T>G (p.Leu384Arg) c.558T>G c.7775T>G (p.Leu2592Arg) c.7580T>G (p.Leu2527Arg) c.7748T>G (p.Leu2583Arg) | |
| 16 | g.89268593A>G | CA397145141 | ANKRD11 | c.7877T>C (p.Leu2626Pro) c.*7680T>C (n.*7680T>C) c.1151T>C (p.Leu384Pro) c.558T>C c.7775T>C (p.Leu2592Pro) c.7580T>C (p.Leu2527Pro) c.7748T>C (p.Leu2583Pro) | |
| 16 | g.89268593A>T | CA397145142 | ANKRD11 | c.7877T>A (p.Leu2626Gln) c.*7680T>A (n.*7680T>A) c.1151T>A (p.Leu384Gln) c.558T>A c.7775T>A (p.Leu2592Gln) c.7580T>A (p.Leu2527Gln) c.7748T>A (p.Leu2583Gln) | |
| 16 | g.89268593_89268596del | CA2695223889 | ANKRD11 | c.7874_7877del (p.Gln2625ArgfsTer16) c.*7677_*7680del (n.*7677_*7680del) c.1148_1151del (p.Gln383ArgfsTer16) c.555_558del c.7772_7775del (p.Gln2591ArgfsTer16) c.7577_7580del (p.Gln2526ArgfsTer16) c.7745_7748del (p.Gln2582ArgfsTer16) | |
| 16 | g.89268594G>A | CA497165661 | ANKRD11 | c.7876C>T (p.Leu2626=) c.*7679C>T (n.*7679C>T) c.1150C>T (p.Leu384=) c.557C>T c.7774C>T (p.Leu2592=) c.7579C>T (p.Leu2527=) c.7747C>T (p.Leu2583=) | |
| 16 | g.89268594G>C | CA397145143 | ANKRD11 | c.7876C>G (p.Leu2626Val) c.*7679C>G (n.*7679C>G) c.1150C>G (p.Leu384Val) c.557C>G c.7774C>G (p.Leu2592Val) c.7579C>G (p.Leu2527Val) c.7747C>G (p.Leu2583Val) | |
| 16 | g.89268594G>T | CA397145144 | ANKRD11 | c.7876C>A (p.Leu2626Met) c.*7679C>A (n.*7679C>A) c.1150C>A (p.Leu384Met) c.557C>A c.7774C>A (p.Leu2592Met) c.7579C>A (p.Leu2527Met) c.7747C>A (p.Leu2583Met) | |
| 16 | g.89268595C>A | CA397145145 | ANKRD11 | c.7875G>T (p.Gln2625His) c.*7678G>T (n.*7678G>T) c.1149G>T (p.Gln383His) c.556G>T c.7773G>T (p.Gln2591His) c.7578G>T (p.Gln2526His) c.7746G>T (p.Gln2582His) | gnomAD v4 |
| 16 | g.89268595C= | CA2241594804 | ANKRD11 | c.7875G= (p.Gln2625=) c.*7678G= (n.*7678G=) c.1149G= (p.Gln383=) c.556G= c.7773G= (p.Gln2591=) c.7578G= (p.Gln2526=) c.7746G= (p.Gln2582=) | |
| 16 | g.89268595C>G | CA397145146 | ANKRD11 | c.7875G>C (p.Gln2625His) c.*7678G>C (n.*7678G>C) c.1149G>C (p.Gln383His) c.556G>C c.7773G>C (p.Gln2591His) c.7578G>C (p.Gln2526His) c.7746G>C (p.Gln2582His) | |
| 16 | g.89268595C>T | CA497165662 | ANKRD11 | c.7875G>A (p.Gln2625=) c.*7678G>A (n.*7678G>A) c.1149G>A (p.Gln383=) c.556G>A c.7773G>A (p.Gln2591=) c.7578G>A (p.Gln2526=) c.7746G>A (p.Gln2582=) | dbSNP gnomAD v4 |
| 16 | g.89268596T>A | CA397145147 | ANKRD11 | c.7874A>T (p.Gln2625Leu) c.*7677A>T (n.*7677A>T) c.1148A>T (p.Gln383Leu) c.555A>T c.7772A>T (p.Gln2591Leu) c.7577A>T (p.Gln2526Leu) c.7745A>T (p.Gln2582Leu) | |
| 16 | g.89268596T>C | CA397145148 | ANKRD11 | c.7874A>G (p.Gln2625Arg) c.*7677A>G (n.*7677A>G) c.1148A>G (p.Gln383Arg) c.555A>G c.7772A>G (p.Gln2591Arg) c.7577A>G (p.Gln2526Arg) c.7745A>G (p.Gln2582Arg) | |
| 16 | g.89268596T>G | CA397145149 | ANKRD11 | c.7874A>C (p.Gln2625Pro) c.*7677A>C (n.*7677A>C) c.1148A>C (p.Gln383Pro) c.555A>C c.7772A>C (p.Gln2591Pro) c.7577A>C (p.Gln2526Pro) c.7745A>C (p.Gln2582Pro) | |
| 16 | g.89268597G>A | CA397145151 | ANKRD11 | c.7873C>T (p.Gln2625Ter) c.*7676C>T (n.*7676C>T) c.1147C>T (p.Gln383Ter) c.554C>T c.7771C>T (p.Gln2591Ter) c.7576C>T (p.Gln2526Ter) c.7744C>T (p.Gln2582Ter) | ClinVar dbSNP gnomAD v4 |
| 16 | g.89268597G>C | CA397145152 | ANKRD11 | c.7873C>G (p.Gln2625Glu) c.*7676C>G (n.*7676C>G) c.1147C>G (p.Gln383Glu) c.554C>G c.7771C>G (p.Gln2591Glu) c.7576C>G (p.Gln2526Glu) c.7744C>G (p.Gln2582Glu) | |
| 16 | g.89268597G= | CA2241594805 | ANKRD11 | c.7873C= (p.Gln2625=) c.*7676C= (n.*7676C=) c.1147C= (p.Gln383=) c.554C= c.7771C= (p.Gln2591=) c.7576C= (p.Gln2526=) c.7744C= (p.Gln2582=) | |
| 16 | g.89268597G>T | CA397145150 | ANKRD11 | c.7873C>A (p.Gln2625Lys) c.*7676C>A (n.*7676C>A) c.1147C>A (p.Gln383Lys) c.554C>A c.7771C>A (p.Gln2591Lys) c.7576C>A (p.Gln2526Lys) c.7744C>A (p.Gln2582Lys) | gnomAD v4 |
| 16 | g.89268598C>A | CA397145154 | ANKRD11 | c.7872G>T (p.Trp2624Cys) c.*7675G>T (n.*7675G>T) c.1146G>T (p.Trp382Cys) c.553G>T c.7770G>T (p.Trp2590Cys) c.7575G>T (p.Trp2525Cys) c.7743G>T (p.Trp2581Cys) | |
| 16 | g.89268598C>G | CA397145156 | ANKRD11 | c.7872G>C (p.Trp2624Cys) c.*7675G>C (n.*7675G>C) c.1146G>C (p.Trp382Cys) c.553G>C c.7770G>C (p.Trp2590Cys) c.7575G>C (p.Trp2525Cys) c.7743G>C (p.Trp2581Cys) | |
| 16 | g.89268598C>T | CA397145158 | ANKRD11 | c.7872G>A (p.Trp2624Ter) c.*7675G>A (n.*7675G>A) c.1146G>A (p.Trp382Ter) c.553G>A c.7770G>A (p.Trp2590Ter) c.7575G>A (p.Trp2525Ter) c.7743G>A (p.Trp2581Ter) | |
| 16 | g.89268601_89268605del | CA2695201157 | ANKRD11 | c.7868_7872del (p.Glu2623AlafsTer?) c.*7671_*7675del (n.*7671_*7675del) c.1142_1146del (p.Glu381AlafsTer?) c.549_553del c.7766_7770del (p.Glu2589AlafsTer?) c.7571_7575del (p.Glu2524AlafsTer?) c.7739_7743del (p.Glu2580AlafsTer?) | ClinVar |
| 16 | g.89268599C>A | CA397145160 | ANKRD11 | c.7871G>T (p.Trp2624Leu) c.*7674G>T (n.*7674G>T) c.1145G>T (p.Trp382Leu) c.552G>T c.7769G>T (p.Trp2590Leu) c.7574G>T (p.Trp2525Leu) c.7742G>T (p.Trp2581Leu) | gnomAD v4 |
| 16 | g.89268599C>G | CA397145161 | ANKRD11 | c.7871G>C (p.Trp2624Ser) c.*7674G>C (n.*7674G>C) c.1145G>C (p.Trp382Ser) c.552G>C c.7769G>C (p.Trp2590Ser) c.7574G>C (p.Trp2525Ser) c.7742G>C (p.Trp2581Ser) | |
| 16 | g.89268599C>T | CA397145163 | ANKRD11 | c.7871G>A (p.Trp2624Ter) c.*7674G>A (n.*7674G>A) c.1145G>A (p.Trp382Ter) c.552G>A c.7769G>A (p.Trp2590Ter) c.7574G>A (p.Trp2525Ter) c.7742G>A (p.Trp2581Ter) | |
| 16 | g.89268600A>C | CA397145168 | ANKRD11 | c.7870T>G (p.Trp2624Gly) c.*7673T>G (n.*7673T>G) c.1144T>G (p.Trp382Gly) c.551T>G c.7768T>G (p.Trp2590Gly) c.7573T>G (p.Trp2525Gly) c.7741T>G (p.Trp2581Gly) | |
| 16 | g.89268600A>G | CA397145165 | ANKRD11 | c.7870T>C (p.Trp2624Arg) c.*7673T>C (n.*7673T>C) c.1144T>C (p.Trp382Arg) c.551T>C c.7768T>C (p.Trp2590Arg) c.7573T>C (p.Trp2525Arg) c.7741T>C (p.Trp2581Arg) | ClinVar dbSNP |
| 16 | g.89268600A>T | CA397145166 | ANKRD11 | c.7870T>A (p.Trp2624Arg) c.*7673T>A (n.*7673T>A) c.1144T>A (p.Trp382Arg) c.551T>A c.7768T>A (p.Trp2590Arg) c.7573T>A (p.Trp2525Arg) c.7741T>A (p.Trp2581Arg) | |
| 16 | g.89268601C>A | CA397145169 | ANKRD11 | c.7869G>T (p.Glu2623Asp) c.*7672G>T (n.*7672G>T) c.1143G>T (p.Glu381Asp) c.550G>T c.7767G>T (p.Glu2589Asp) c.7572G>T (p.Glu2524Asp) c.7740G>T (p.Glu2580Asp) | gnomAD v4 |
| 16 | g.89268601C>G | CA397145171 | ANKRD11 | c.7869G>C (p.Glu2623Asp) c.*7672G>C (n.*7672G>C) c.1143G>C (p.Glu381Asp) c.550G>C c.7767G>C (p.Glu2589Asp) c.7572G>C (p.Glu2524Asp) c.7740G>C (p.Glu2580Asp) | |
| 16 | g.89268601C>T | CA497165665 | ANKRD11 | c.7869G>A (p.Glu2623=) c.*7672G>A (n.*7672G>A) c.1143G>A (p.Glu381=) c.550G>A c.7767G>A (p.Glu2589=) c.7572G>A (p.Glu2524=) c.7740G>A (p.Glu2580=) | |
| 16 | g.89268602T>A | CA397145173 | ANKRD11 | c.7868A>T (p.Glu2623Val) c.*7671A>T (n.*7671A>T) c.1142A>T (p.Glu381Val) c.549A>T c.7766A>T (p.Glu2589Val) c.7571A>T (p.Glu2524Val) c.7739A>T (p.Glu2580Val) | |
| 16 | g.89268602T>C | CA397145175 | ANKRD11 | c.7868A>G (p.Glu2623Gly) c.*7671A>G (n.*7671A>G) c.1142A>G (p.Glu381Gly) c.549A>G c.7766A>G (p.Glu2589Gly) c.7571A>G (p.Glu2524Gly) c.7739A>G (p.Glu2580Gly) | |
| 16 | g.89268602T>G | CA397145176 | ANKRD11 | c.7868A>C (p.Glu2623Ala) c.*7671A>C (n.*7671A>C) c.1142A>C (p.Glu381Ala) c.549A>C c.7766A>C (p.Glu2589Ala) c.7571A>C (p.Glu2524Ala) c.7739A>C (p.Glu2580Ala) | |
| 16 | g.89268603C>A | CA397145178 | ANKRD11 | c.7867G>T (p.Glu2623Ter) c.*7670G>T (n.*7670G>T) c.1141G>T (p.Glu381Ter) c.548G>T c.7765G>T (p.Glu2589Ter) c.7570G>T (p.Glu2524Ter) c.7738G>T (p.Glu2580Ter) | gnomAD v4 |
| 16 | g.89268603C>G | CA397145181 | ANKRD11 | c.7867G>C (p.Glu2623Gln) c.*7670G>C (n.*7670G>C) c.1141G>C (p.Glu381Gln) c.548G>C c.7765G>C (p.Glu2589Gln) c.7570G>C (p.Glu2524Gln) c.7738G>C (p.Glu2580Gln) | |
| 16 | g.89268603C>T | CA397145179 | ANKRD11 | c.7867G>A (p.Glu2623Lys) c.*7670G>A (n.*7670G>A) c.1141G>A (p.Glu381Lys) c.548G>A c.7765G>A (p.Glu2589Lys) c.7570G>A (p.Glu2524Lys) c.7738G>A (p.Glu2580Lys) | gnomAD v4 |
| 16 | g.89268604C>A | CA397145183 | ANKRD11 | c.7866G>T (p.Met2622Ile) c.*7669G>T (n.*7669G>T) c.1140G>T (p.Met380Ile) c.547G>T c.7764G>T (p.Met2588Ile) c.7569G>T (p.Met2523Ile) c.7737G>T (p.Met2579Ile) | gnomAD v4 |
| 16 | g.89268604C>G | CA397145187 | ANKRD11 | c.7866G>C (p.Met2622Ile) c.*7669G>C (n.*7669G>C) c.1140G>C (p.Met380Ile) c.547G>C c.7764G>C (p.Met2588Ile) c.7569G>C (p.Met2523Ile) c.7737G>C (p.Met2579Ile) | |
| 16 | g.89268604C>T | CA397145185 | ANKRD11 | c.7866G>A (p.Met2622Ile) c.*7669G>A (n.*7669G>A) c.1140G>A (p.Met380Ile) c.547G>A c.7764G>A (p.Met2588Ile) c.7569G>A (p.Met2523Ile) c.7737G>A (p.Met2579Ile) | |
| 16 | g.89268605A>C | CA397145189 | ANKRD11 | c.7865T>G (p.Met2622Arg) c.*7668T>G (n.*7668T>G) c.1139T>G (p.Met380Arg) c.546T>G c.7763T>G (p.Met2588Arg) c.7568T>G (p.Met2523Arg) c.7736T>G (p.Met2579Arg) | |
| 16 | g.89268605A>G | CA397145192 | ANKRD11 | c.7865T>C (p.Met2622Thr) c.*7668T>C (n.*7668T>C) c.1139T>C (p.Met380Thr) c.546T>C c.7763T>C (p.Met2588Thr) c.7568T>C (p.Met2523Thr) c.7736T>C (p.Met2579Thr) | |
| 16 | g.89268605A>T | CA397145191 | ANKRD11 | c.7865T>A (p.Met2622Lys) c.*7668T>A (n.*7668T>A) c.1139T>A (p.Met380Lys) c.546T>A c.7763T>A (p.Met2588Lys) c.7568T>A (p.Met2523Lys) c.7736T>A (p.Met2579Lys) | gnomAD v4 |
| 16 | g.89268606T>A | CA397145194 | ANKRD11 | c.7864A>T (p.Met2622Leu) c.*7667A>T (n.*7667A>T) c.1138A>T (p.Met380Leu) c.545A>T c.7762A>T (p.Met2588Leu) c.7567A>T (p.Met2523Leu) c.7735A>T (p.Met2579Leu) | |
| 16 | g.89268606T>C | CA397145196 | ANKRD11 | c.7864A>G (p.Met2622Val) c.*7667A>G (n.*7667A>G) c.1138A>G (p.Met380Val) c.545A>G c.7762A>G (p.Met2588Val) c.7567A>G (p.Met2523Val) c.7735A>G (p.Met2579Val) | |
| 16 | g.89268606T>G | CA397145195 | ANKRD11 | c.7864A>C (p.Met2622Leu) c.*7667A>C (n.*7667A>C) c.1138A>C (p.Met380Leu) c.545A>C c.7762A>C (p.Met2588Leu) c.7567A>C (p.Met2523Leu) c.7735A>C (p.Met2579Leu) | gnomAD v4 |
| 16 | g.89268607C>A | CA397145198 | ANKRD11 | c.7863G>T (p.Arg2621Ser) c.*7666G>T (n.*7666G>T) c.1137G>T (p.Arg379Ser) c.544G>T c.7761G>T (p.Arg2587Ser) c.7566G>T (p.Arg2522Ser) c.7734G>T (p.Arg2578Ser) | gnomAD v4 |
| 16 | g.89268607C= | CA2241594806 | ANKRD11 | c.7863G= (p.Arg2621=) c.*7666G= (n.*7666G=) c.1137G= (p.Arg379=) c.544G= c.7761G= (p.Arg2587=) c.7566G= (p.Arg2522=) c.7734G= (p.Arg2578=) | |
| 16 | g.89268607C>G | CA397145200 | ANKRD11 | c.7863G>C (p.Arg2621Ser) c.*7666G>C (n.*7666G>C) c.1137G>C (p.Arg379Ser) c.544G>C c.7761G>C (p.Arg2587Ser) c.7566G>C (p.Arg2522Ser) c.7734G>C (p.Arg2578Ser) | |
| 16 | g.89268607C>T | CA497165670 | ANKRD11 | c.7863G>A (p.Arg2621=) c.*7666G>A (n.*7666G>A) c.1137G>A (p.Arg379=) c.544G>A c.7761G>A (p.Arg2587=) c.7566G>A (p.Arg2522=) c.7734G>A (p.Arg2578=) | dbSNP gnomAD v2 gnomAD v4 |
| 16 | g.89268608C>A | CA397145202 | ANKRD11 | c.7862G>T (p.Arg2621Met) c.*7665G>T (n.*7665G>T) c.1136G>T (p.Arg379Met) c.543G>T c.7760G>T (p.Arg2587Met) c.7565G>T (p.Arg2522Met) c.7733G>T (p.Arg2578Met) | gnomAD v4 |
| 16 | g.89268608C>G | CA397145205 | ANKRD11 | c.7862G>C (p.Arg2621Thr) c.*7665G>C (n.*7665G>C) c.1136G>C (p.Arg379Thr) c.543G>C c.7760G>C (p.Arg2587Thr) c.7565G>C (p.Arg2522Thr) c.7733G>C (p.Arg2578Thr) | |
| 16 | g.89268608C>T | CA397145204 | ANKRD11 | c.7862G>A (p.Arg2621Lys) c.*7665G>A (n.*7665G>A) c.1136G>A (p.Arg379Lys) c.543G>A c.7760G>A (p.Arg2587Lys) c.7565G>A (p.Arg2522Lys) c.7733G>A (p.Arg2578Lys) | gnomAD v4 |
| 16 | g.89268609T>A | CA397145207 | ANKRD11 | c.7861A>T (p.Arg2621Trp) c.*7664A>T (n.*7664A>T) c.1135A>T (p.Arg379Trp) c.542A>T c.7759A>T (p.Arg2587Trp) c.7564A>T (p.Arg2522Trp) c.7732A>T (p.Arg2578Trp) | |
| 16 | g.89268609T>C | CA397145209 | ANKRD11 | c.7861A>G (p.Arg2621Gly) c.*7664A>G (n.*7664A>G) c.1135A>G (p.Arg379Gly) c.542A>G c.7759A>G (p.Arg2587Gly) c.7564A>G (p.Arg2522Gly) c.7732A>G (p.Arg2578Gly) | |
| 16 | g.89268609T>G | CA497165672 | ANKRD11 | c.7861A>C (p.Arg2621=) c.*7664A>C (n.*7664A>C) c.1135A>C (p.Arg379=) c.542A>C c.7759A>C (p.Arg2587=) c.7564A>C (p.Arg2522=) c.7732A>C (p.Arg2578=) | |
| 16 | g.89268610C>A | CA397145211 | ANKRD11 | c.7860G>T (p.Gln2620His) c.*7663G>T (n.*7663G>T) c.1134G>T (p.Gln378His) c.541G>T c.7758G>T (p.Gln2586His) c.7563G>T (p.Gln2521His) c.7731G>T (p.Gln2577His) | gnomAD v4 |
| 16 | g.89268610C= | CA2241594807 | ANKRD11 | c.7860G= (p.Gln2620=) c.*7663G= (n.*7663G=) c.1134G= (p.Gln378=) c.541G= c.7758G= (p.Gln2586=) c.7563G= (p.Gln2521=) c.7731G= (p.Gln2577=) | |
| 16 | g.89268610C>G | CA397145213 | ANKRD11 | c.7860G>C (p.Gln2620His) c.*7663G>C (n.*7663G>C) c.1134G>C (p.Gln378His) c.541G>C c.7758G>C (p.Gln2586His) c.7563G>C (p.Gln2521His) c.7731G>C (p.Gln2577His) | dbSNP gnomAD v2 gnomAD v4 |
| 16 | g.89268610C>T | CA497165673 | ANKRD11 | c.7860G>A (p.Gln2620=) c.*7663G>A (n.*7663G>A) c.1134G>A (p.Gln378=) c.541G>A c.7758G>A (p.Gln2586=) c.7563G>A (p.Gln2521=) c.7731G>A (p.Gln2577=) | |
| 16 | g.89268611T>A | CA397145214 | ANKRD11 | c.7859A>T (p.Gln2620Leu) c.*7662A>T (n.*7662A>T) c.1133A>T (p.Gln378Leu) c.540A>T c.7757A>T (p.Gln2586Leu) c.7562A>T (p.Gln2521Leu) c.7730A>T (p.Gln2577Leu) | gnomAD v4 |
| 16 | g.89268611T>C | CA397145215 | ANKRD11 | c.7859A>G (p.Gln2620Arg) c.*7662A>G (n.*7662A>G) c.1133A>G (p.Gln378Arg) c.540A>G c.7757A>G (p.Gln2586Arg) c.7562A>G (p.Gln2521Arg) c.7730A>G (p.Gln2577Arg) | gnomAD v4 |
| 16 | g.89268611T>G | CA397145217 | ANKRD11 | c.7859A>C (p.Gln2620Pro) c.*7662A>C (n.*7662A>C) c.1133A>C (p.Gln378Pro) c.540A>C c.7757A>C (p.Gln2586Pro) c.7562A>C (p.Gln2521Pro) c.7730A>C (p.Gln2577Pro) | |
| 16 | g.89268612G>A | CA397145218 | ANKRD11 | c.7858C>T (p.Gln2620Ter) c.*7661C>T (n.*7661C>T) c.1132C>T (p.Gln378Ter) c.539C>T c.7756C>T (p.Gln2586Ter) c.7561C>T (p.Gln2521Ter) c.7729C>T (p.Gln2577Ter) | gnomAD v4 |
| 16 | g.89268612G>C | CA397145220 | ANKRD11 | c.7858C>G (p.Gln2620Glu) c.*7661C>G (n.*7661C>G) c.1132C>G (p.Gln378Glu) c.539C>G c.7756C>G (p.Gln2586Glu) c.7561C>G (p.Gln2521Glu) c.7729C>G (p.Gln2577Glu) | |
| 16 | g.89268612G>T | CA397145222 | ANKRD11 | c.7858C>A (p.Gln2620Lys) c.*7661C>A (n.*7661C>A) c.1132C>A (p.Gln378Lys) c.539C>A c.7756C>A (p.Gln2586Lys) c.7561C>A (p.Gln2521Lys) c.7729C>A (p.Gln2577Lys) | |
| 16 | g.89268613C>A | CA497165675 | ANKRD11 | c.7857G>T (p.Val2619=) c.*7660G>T (n.*7660G>T) c.1131G>T (p.Val377=) c.538G>T c.7755G>T (p.Val2585=) c.7560G>T (p.Val2520=) c.7728G>T (p.Val2576=) | |
| 16 | g.89268613C>G | CA497165676 | ANKRD11 | c.7857G>C (p.Val2619=) c.*7660G>C (n.*7660G>C) c.1131G>C (p.Val377=) c.538G>C c.7755G>C (p.Val2585=) c.7560G>C (p.Val2520=) c.7728G>C (p.Val2576=) | |
| 16 | g.89268613C>T | CA497165677 | ANKRD11 | c.7857G>A (p.Val2619=) c.*7660G>A (n.*7660G>A) c.1131G>A (p.Val377=) c.538G>A c.7755G>A (p.Val2585=) c.7560G>A (p.Val2520=) c.7728G>A (p.Val2576=) | gnomAD v4 |
| 16 | g.89268614A>C | CA397145228 | ANKRD11 | c.7856T>G (p.Val2619Gly) c.*7659T>G (n.*7659T>G) c.1130T>G (p.Val377Gly) c.537T>G c.7754T>G (p.Val2585Gly) c.7559T>G (p.Val2520Gly) c.7727T>G (p.Val2576Gly) | |
| 16 | g.89268614A>G | CA397145226 | ANKRD11 | c.7856T>C (p.Val2619Ala) c.*7659T>C (n.*7659T>C) c.1130T>C (p.Val377Ala) c.537T>C c.7754T>C (p.Val2585Ala) c.7559T>C (p.Val2520Ala) c.7727T>C (p.Val2576Ala) | |
| 16 | g.89268614A>T | CA397145224 | ANKRD11 | c.7856T>A (p.Val2619Glu) c.*7659T>A (n.*7659T>A) c.1130T>A (p.Val377Glu) c.537T>A c.7754T>A (p.Val2585Glu) c.7559T>A (p.Val2520Glu) c.7727T>A (p.Val2576Glu) | |
| 16 | g.89268615C>A | CA397145230 | ANKRD11 | c.7855G>T (p.Val2619Leu) c.*7658G>T (n.*7658G>T) c.1129G>T (p.Val377Leu) c.536G>T c.7753G>T (p.Val2585Leu) c.7558G>T (p.Val2520Leu) c.7726G>T (p.Val2576Leu) | ClinVar dbSNP gnomAD v4 |
| 16 | g.89268615C= | CA2241594808 | ANKRD11 | c.7855G= (p.Val2619=) c.*7658G= (n.*7658G=) c.1129G= (p.Val377=) c.536G= c.7753G= (p.Val2585=) c.7558G= (p.Val2520=) c.7726G= (p.Val2576=) | |
| 16 | g.89268615C>G | CA397145232 | ANKRD11 | c.7855G>C (p.Val2619Leu) c.*7658G>C (n.*7658G>C) c.1129G>C (p.Val377Leu) c.536G>C c.7753G>C (p.Val2585Leu) c.7558G>C (p.Val2520Leu) c.7726G>C (p.Val2576Leu) | |
| 16 | g.89268615C>T | CA397145234 | ANKRD11 | c.7855G>A (p.Val2619Met) c.*7658G>A (n.*7658G>A) c.1129G>A (p.Val377Met) c.536G>A c.7753G>A (p.Val2585Met) c.7558G>A (p.Val2520Met) c.7726G>A (p.Val2576Met) | ClinVar gnomAD v4 |
| 16 | g.89268616G>A | CA497165681 | ANKRD11 | c.7854C>T (p.Ala2618=) c.*7657C>T (n.*7657C>T) c.1128C>T (p.Ala376=) c.535C>T c.7752C>T (p.Ala2584=) c.7557C>T (p.Ala2519=) c.7725C>T (p.Ala2575=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.89268616G>C | CA497165683 | ANKRD11 | c.7854C>G (p.Ala2618=) c.*7657C>G (n.*7657C>G) c.1128C>G (p.Ala376=) c.535C>G c.7752C>G (p.Ala2584=) c.7557C>G (p.Ala2519=) c.7725C>G (p.Ala2575=) | dbSNP gnomAD v3 gnomAD v4 |
| 16 | g.89268616G= | CA2241594809 | ANKRD11 | c.7854C= (p.Ala2618=) c.*7657C= (n.*7657C=) c.1128C= (p.Ala376=) c.535C= c.7752C= (p.Ala2584=) c.7557C= (p.Ala2519=) c.7725C= (p.Ala2575=) | |
| 16 | g.89268616G>T | CA497165682 | ANKRD11 | c.7854C>A (p.Ala2618=) c.*7657C>A (n.*7657C>A) c.1128C>A (p.Ala376=) c.535C>A c.7752C>A (p.Ala2584=) c.7557C>A (p.Ala2519=) c.7725C>A (p.Ala2575=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.89268617G>A | CA397145236 | ANKRD11 | c.7853C>T (p.Ala2618Val) c.*7656C>T (n.*7656C>T) c.1127C>T (p.Ala376Val) c.534C>T c.7751C>T (p.Ala2584Val) c.7556C>T (p.Ala2519Val) c.7724C>T (p.Ala2575Val) | gnomAD v4 COSMIC |
| 16 | g.89268617G>C | CA397145237 | ANKRD11 | c.7853C>G (p.Ala2618Gly) c.*7656C>G (n.*7656C>G) c.1127C>G (p.Ala376Gly) c.534C>G c.7751C>G (p.Ala2584Gly) c.7556C>G (p.Ala2519Gly) c.7724C>G (p.Ala2575Gly) | |
| 16 | g.89268617G>T | CA397145239 | ANKRD11 | c.7853C>A (p.Ala2618Asp) c.*7656C>A (n.*7656C>A) c.1127C>A (p.Ala376Asp) c.534C>A c.7751C>A (p.Ala2584Asp) c.7556C>A (p.Ala2519Asp) c.7724C>A (p.Ala2575Asp) | gnomAD v4 |
| 16 | g.89268618C>A | CA397145241 | ANKRD11 | c.7852G>T (p.Ala2618Ser) c.*7655G>T (n.*7655G>T) c.1126G>T (p.Ala376Ser) c.533G>T c.7750G>T (p.Ala2584Ser) c.7555G>T (p.Ala2519Ser) c.7723G>T (p.Ala2575Ser) | gnomAD v4 |
| 16 | g.89268618C>G | CA397145243 | ANKRD11 | c.7852G>C (p.Ala2618Pro) c.*7655G>C (n.*7655G>C) c.1126G>C (p.Ala376Pro) c.533G>C c.7750G>C (p.Ala2584Pro) c.7555G>C (p.Ala2519Pro) c.7723G>C (p.Ala2575Pro) | |
| 16 | g.89268618C>T | CA397145245 | ANKRD11 | c.7852G>A (p.Ala2618Thr) c.*7655G>A (n.*7655G>A) c.1126G>A (p.Ala376Thr) c.533G>A c.7750G>A (p.Ala2584Thr) c.7555G>A (p.Ala2519Thr) c.7723G>A (p.Ala2575Thr) | ClinVar gnomAD v4 |
| 16 | g.89268619G>A | CA497165685 | ANKRD11 | c.7851C>T (p.Asn2617=) c.*7654C>T (n.*7654C>T) c.1125C>T (p.Asn375=) c.532C>T c.7749C>T (p.Asn2583=) c.7554C>T (p.Asn2518=) c.7722C>T (p.Asn2574=) | dbSNP gnomAD v2 gnomAD v4 |
| 16 | g.89268619G>C | CA397145247 | ANKRD11 | c.7851C>G (p.Asn2617Lys) c.*7654C>G (n.*7654C>G) c.1125C>G (p.Asn375Lys) c.532C>G c.7749C>G (p.Asn2583Lys) c.7554C>G (p.Asn2518Lys) c.7722C>G (p.Asn2574Lys) | |
| 16 | g.89268619G= | CA2241594810 | ANKRD11 | c.7851C= (p.Asn2617=) c.*7654C= (n.*7654C=) c.1125C= (p.Asn375=) c.532C= c.7749C= (p.Asn2583=) c.7554C= (p.Asn2518=) c.7722C= (p.Asn2574=) | |
| 16 | g.89268619G>T | CA397145248 | ANKRD11 | c.7851C>A (p.Asn2617Lys) c.*7654C>A (n.*7654C>A) c.1125C>A (p.Asn375Lys) c.532C>A c.7749C>A (p.Asn2583Lys) c.7554C>A (p.Asn2518Lys) c.7722C>A (p.Asn2574Lys) | gnomAD v4 |
| 16 | g.89268620T>A | CA397145252 | ANKRD11 | c.7850A>T (p.Asn2617Ile) c.*7653A>T (n.*7653A>T) c.1124A>T (p.Asn375Ile) c.531A>T c.7748A>T (p.Asn2583Ile) c.7553A>T (p.Asn2518Ile) c.7721A>T (p.Asn2574Ile) | |
| 16 | g.89268620T>C | CA397145251 | ANKRD11 | c.7850A>G (p.Asn2617Ser) c.*7653A>G (n.*7653A>G) c.1124A>G (p.Asn375Ser) c.531A>G c.7748A>G (p.Asn2583Ser) c.7553A>G (p.Asn2518Ser) c.7721A>G (p.Asn2574Ser) | |
| 16 | g.89268620T>G | CA397145250 | ANKRD11 | c.7850A>C (p.Asn2617Thr) c.*7653A>C (n.*7653A>C) c.1124A>C (p.Asn375Thr) c.531A>C c.7748A>C (p.Asn2583Thr) c.7553A>C (p.Asn2518Thr) c.7721A>C (p.Asn2574Thr) | |
| 16 | g.89268621T>A | CA397145254 | ANKRD11 | c.7849A>T (p.Asn2617Tyr) c.*7652A>T (n.*7652A>T) c.1123A>T (p.Asn375Tyr) c.530A>T c.7747A>T (p.Asn2583Tyr) c.7552A>T (p.Asn2518Tyr) c.7720A>T (p.Asn2574Tyr) | |
| 16 | g.89268621T>C | CA397145256 | ANKRD11 | c.7849A>G (p.Asn2617Asp) c.*7652A>G (n.*7652A>G) c.1123A>G (p.Asn375Asp) c.530A>G c.7747A>G (p.Asn2583Asp) c.7552A>G (p.Asn2518Asp) c.7720A>G (p.Asn2574Asp) | |
| 16 | g.89268621T>G | CA397145258 | ANKRD11 | c.7849A>C (p.Asn2617His) c.*7652A>C (n.*7652A>C) c.1123A>C (p.Asn375His) c.530A>C c.7747A>C (p.Asn2583His) c.7552A>C (p.Asn2518His) c.7720A>C (p.Asn2574His) | gnomAD v4 |
| 16 | g.89268622C>A | CA497165689 | ANKRD11 | c.7848G>T (p.Leu2616=) c.*7651G>T (n.*7651G>T) c.1122G>T (p.Leu374=) c.529G>T c.7746G>T (p.Leu2582=) c.7551G>T (p.Leu2517=) c.7719G>T (p.Leu2573=) | dbSNP gnomAD v2 gnomAD v4 |
| 16 | g.89268622C= | CA2241594811 | ANKRD11 | c.7848G= (p.Leu2616=) c.*7651G= (n.*7651G=) c.1122G= (p.Leu374=) c.529G= c.7746G= (p.Leu2582=) c.7551G= (p.Leu2517=) c.7719G= (p.Leu2573=) | |
| 16 | g.89268622C>G | CA8240980 | ANKRD11 | c.7848G>C (p.Leu2616=) c.*7651G>C (n.*7651G>C) c.1122G>C (p.Leu374=) c.529G>C c.7746G>C (p.Leu2582=) c.7551G>C (p.Leu2517=) c.7719G>C (p.Leu2573=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.89268622C>T | CA497165690 | ANKRD11 | c.7848G>A (p.Leu2616=) c.*7651G>A (n.*7651G>A) c.1122G>A (p.Leu374=) c.529G>A c.7746G>A (p.Leu2582=) c.7551G>A (p.Leu2517=) c.7719G>A (p.Leu2573=) | dbSNP gnomAD v2 gnomAD v4 |
| 16 | g.89268623A= | CA2241594812 | ANKRD11 | c.7847T= (p.Leu2616=) c.*7650T= (n.*7650T=) c.1121T= (p.Leu374=) c.528T= c.7745T= (p.Leu2582=) c.7550T= (p.Leu2517=) c.7718T= (p.Leu2573=) | |
| 16 | g.89268623A>C | CA397145262 | ANKRD11 | c.7847T>G (p.Leu2616Arg) c.*7650T>G (n.*7650T>G) c.1121T>G (p.Leu374Arg) c.528T>G c.7745T>G (p.Leu2582Arg) c.7550T>G (p.Leu2517Arg) c.7718T>G (p.Leu2573Arg) | |
| 16 | g.89268623A>G | CA397145263 | ANKRD11 | c.7847T>C (p.Leu2616Pro) c.*7650T>C (n.*7650T>C) c.1121T>C (p.Leu374Pro) c.528T>C c.7745T>C (p.Leu2582Pro) c.7550T>C (p.Leu2517Pro) c.7718T>C (p.Leu2573Pro) | ClinVar dbSNP gnomAD v4 |
| 16 | g.89268623A>T | CA397145265 | ANKRD11 | c.7847T>A (p.Leu2616Gln) c.*7650T>A (n.*7650T>A) c.1121T>A (p.Leu374Gln) c.528T>A c.7745T>A (p.Leu2582Gln) c.7550T>A (p.Leu2517Gln) c.7718T>A (p.Leu2573Gln) | gnomAD v4 |
| 16 | g.89268624G>A | CA497165692 | ANKRD11 | c.7846C>T (p.Leu2616=) c.*7649C>T (n.*7649C>T) c.1120C>T (p.Leu374=) c.527C>T c.7744C>T (p.Leu2582=) c.7549C>T (p.Leu2517=) c.7717C>T (p.Leu2573=) | dbSNP gnomAD v4 |
| 16 | g.89268624G>C | CA397145267 | ANKRD11 | c.7846C>G (p.Leu2616Val) c.*7649C>G (n.*7649C>G) c.1120C>G (p.Leu374Val) c.527C>G c.7744C>G (p.Leu2582Val) c.7549C>G (p.Leu2517Val) c.7717C>G (p.Leu2573Val) | |
| 16 | g.89268624G= | CA2241594813 | ANKRD11 | c.7846C= (p.Leu2616=) c.*7649C= (n.*7649C=) c.1120C= (p.Leu374=) c.527C= c.7744C= (p.Leu2582=) c.7549C= (p.Leu2517=) c.7717C= (p.Leu2573=) | |
| 16 | g.89268624G>T | CA397145268 | ANKRD11 | c.7846C>A (p.Leu2616Met) c.*7649C>A (n.*7649C>A) c.1120C>A (p.Leu374Met) c.527C>A c.7744C>A (p.Leu2582Met) c.7549C>A (p.Leu2517Met) c.7717C>A (p.Leu2573Met) | gnomAD v4 |
| 16 | g.89268625G>A | CA497165695 | ANKRD11 | c.7845C>T (p.Ala2615=) c.*7648C>T (n.*7648C>T) c.1119C>T (p.Ala373=) c.526C>T c.7743C>T (p.Ala2581=) c.7548C>T (p.Ala2516=) c.7716C>T (p.Ala2572=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 16 | g.89268625G>C | CA497165694 | ANKRD11 | c.7845C>G (p.Ala2615=) c.*7648C>G (n.*7648C>G) c.1119C>G (p.Ala373=) c.526C>G c.7743C>G (p.Ala2581=) c.7548C>G (p.Ala2516=) c.7716C>G (p.Ala2572=) | |
| 16 | g.89268625G= | CA2241594814 | ANKRD11 | c.7845C= (p.Ala2615=) c.*7648C= (n.*7648C=) c.1119C= (p.Ala373=) c.526C= c.7743C= (p.Ala2581=) c.7548C= (p.Ala2516=) c.7716C= (p.Ala2572=) | |
| 16 | g.89268625G>T | CA497165693 | ANKRD11 | c.7845C>A (p.Ala2615=) c.*7648C>A (n.*7648C>A) c.1119C>A (p.Ala373=) c.526C>A c.7743C>A (p.Ala2581=) c.7548C>A (p.Ala2516=) c.7716C>A (p.Ala2572=) | |
| 16 | g.89268626G>A | CA397145271 | ANKRD11 | c.7844C>T (p.Ala2615Val) c.*7647C>T (n.*7647C>T) c.1118C>T (p.Ala373Val) c.525C>T c.7742C>T (p.Ala2581Val) c.7547C>T (p.Ala2516Val) c.7715C>T (p.Ala2572Val) | ClinVar gnomAD v4 |
| 16 | g.89268626G>C | CA397145273 | ANKRD11 | c.7844C>G (p.Ala2615Gly) c.*7647C>G (n.*7647C>G) c.1118C>G (p.Ala373Gly) c.525C>G c.7742C>G (p.Ala2581Gly) c.7547C>G (p.Ala2516Gly) c.7715C>G (p.Ala2572Gly) | |
| 16 | g.89268626G>T | CA397145274 | ANKRD11 | c.7844C>A (p.Ala2615Asp) c.*7647C>A (n.*7647C>A) c.1118C>A (p.Ala373Asp) c.525C>A c.7742C>A (p.Ala2581Asp) c.7547C>A (p.Ala2516Asp) c.7715C>A (p.Ala2572Asp) | gnomAD v4 |
| 16 | g.89268627C>A | CA397145279 | ANKRD11 | c.7843G>T (p.Ala2615Ser) c.*7646G>T (n.*7646G>T) c.1117G>T (p.Ala373Ser) c.524G>T c.7741G>T (p.Ala2581Ser) c.7546G>T (p.Ala2516Ser) c.7714G>T (p.Ala2572Ser) | gnomAD v4 |
| 16 | g.89268627C= | CA2241594815 | ANKRD11 | c.7843G= (p.Ala2615=) c.*7646G= (n.*7646G=) c.1117G= (p.Ala373=) c.524G= c.7741G= (p.Ala2581=) c.7546G= (p.Ala2516=) c.7714G= (p.Ala2572=) | |
| 16 | g.89268627C>G | CA397145276 | ANKRD11 | c.7843G>C (p.Ala2615Pro) c.*7646G>C (n.*7646G>C) c.1117G>C (p.Ala373Pro) c.524G>C c.7741G>C (p.Ala2581Pro) c.7546G>C (p.Ala2516Pro) c.7714G>C (p.Ala2572Pro) | |
| 16 | g.89268627C>T | CA286503927 | ANKRD11 | c.7843G>A (p.Ala2615Thr) c.*7646G>A (n.*7646G>A) c.1117G>A (p.Ala373Thr) c.524G>A c.7741G>A (p.Ala2581Thr) c.7546G>A (p.Ala2516Thr) c.7714G>A (p.Ala2572Thr) | dbSNP gnomAD v4 |
| 16 | g.89268628C>A | CA497165697 | ANKRD11 | c.7842G>T (p.Ala2614=) c.*7645G>T (n.*7645G>T) c.1116G>T (p.Ala372=) c.523G>T c.7740G>T (p.Ala2580=) c.7545G>T (p.Ala2515=) c.7713G>T (p.Ala2571=) | gnomAD v4 |
| 16 | g.89268628C= | CA2241594816 | ANKRD11 | c.7842G= (p.Ala2614=) c.*7645G= (n.*7645G=) c.1116G= (p.Ala372=) c.523G= c.7740G= (p.Ala2580=) c.7545G= (p.Ala2515=) c.7713G= (p.Ala2571=) | |
| 16 | g.89268628C>G | CA497165698 | ANKRD11 | c.7842G>C (p.Ala2614=) c.*7645G>C (n.*7645G>C) c.1116G>C (p.Ala372=) c.523G>C c.7740G>C (p.Ala2580=) c.7545G>C (p.Ala2515=) c.7713G>C (p.Ala2571=) | gnomAD v4 |
| 16 | g.89268628C>T | CA286503929 | ANKRD11 | c.7842G>A (p.Ala2614=) c.*7645G>A (n.*7645G>A) c.1116G>A (p.Ala372=) c.523G>A c.7740G>A (p.Ala2580=) c.7545G>A (p.Ala2515=) c.7713G>A (p.Ala2571=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 16 | g.89268629G>A | CA397145282 | ANKRD11 | c.7841C>T (p.Ala2614Val) c.*7644C>T (n.*7644C>T) c.1115C>T (p.Ala372Val) c.522C>T c.7739C>T (p.Ala2580Val) c.7544C>T (p.Ala2515Val) c.7712C>T (p.Ala2571Val) | gnomAD v4 |
| 16 | g.89268629G>C | CA397145283 | ANKRD11 | c.7841C>G (p.Ala2614Gly) c.*7644C>G (n.*7644C>G) c.1115C>G (p.Ala372Gly) c.522C>G c.7739C>G (p.Ala2580Gly) c.7544C>G (p.Ala2515Gly) c.7712C>G (p.Ala2571Gly) | |
| 16 | g.89268629G>T | CA397145285 | ANKRD11 | c.7841C>A (p.Ala2614Glu) c.*7644C>A (n.*7644C>A) c.1115C>A (p.Ala372Glu) c.522C>A c.7739C>A (p.Ala2580Glu) c.7544C>A (p.Ala2515Glu) c.7712C>A (p.Ala2571Glu) | gnomAD v4 |
| 16 | g.89268630C>A | CA397145287 | ANKRD11 | c.7840G>T (p.Ala2614Ser) c.*7643G>T (n.*7643G>T) c.1114G>T (p.Ala372Ser) c.521G>T c.7738G>T (p.Ala2580Ser) c.7543G>T (p.Ala2515Ser) c.7711G>T (p.Ala2571Ser) | gnomAD v4 |
| 16 | g.89268630C>G | CA397145289 | ANKRD11 | c.7840G>C (p.Ala2614Pro) c.*7643G>C (n.*7643G>C) c.1114G>C (p.Ala372Pro) c.521G>C c.7738G>C (p.Ala2580Pro) c.7543G>C (p.Ala2515Pro) c.7711G>C (p.Ala2571Pro) | |
| 16 | g.89268630C>T | CA397145291 | ANKRD11 | c.7840G>A (p.Ala2614Thr) c.*7643G>A (n.*7643G>A) c.1114G>A (p.Ala372Thr) c.521G>A c.7738G>A (p.Ala2580Thr) c.7543G>A (p.Ala2515Thr) c.7711G>A (p.Ala2571Thr) | gnomAD v4 COSMIC |
| 16 | g.89268631G>A | CA497165699 | ANKRD11 | c.7839C>T (p.Ala2613=) c.*7642C>T (n.*7642C>T) c.1113C>T (p.Ala371=) c.520C>T c.7737C>T (p.Ala2579=) c.7542C>T (p.Ala2514=) c.7710C>T (p.Ala2570=) | gnomAD v4 |
| 16 | g.89268631G>C | CA8240981 | ANKRD11 | c.7839C>G (p.Ala2613=) c.*7642C>G (n.*7642C>G) c.1113C>G (p.Ala371=) c.520C>G c.7737C>G (p.Ala2579=) c.7542C>G (p.Ala2514=) c.7710C>G (p.Ala2570=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.89268631G= | CA2241594817 | ANKRD11 | c.7839C= (p.Ala2613=) c.*7642C= (n.*7642C=) c.1113C= (p.Ala371=) c.520C= c.7737C= (p.Ala2579=) c.7542C= (p.Ala2514=) c.7710C= (p.Ala2570=) | |
| 16 | g.89268631G>T | CA497165701 | ANKRD11 | c.7839C>A (p.Ala2613=) c.*7642C>A (n.*7642C>A) c.1113C>A (p.Ala371=) c.520C>A c.7737C>A (p.Ala2579=) c.7542C>A (p.Ala2514=) c.7710C>A (p.Ala2570=) | gnomAD v4 |
| 16 | g.89268632G>A | CA397145294 | ANKRD11 | c.7838C>T (p.Ala2613Val) c.*7641C>T (n.*7641C>T) c.1112C>T (p.Ala371Val) c.519C>T c.7736C>T (p.Ala2579Val) c.7541C>T (p.Ala2514Val) c.7709C>T (p.Ala2570Val) | gnomAD v4 |
| 16 | g.89268632G>C | CA397145295 | ANKRD11 | c.7838C>G (p.Ala2613Gly) c.*7641C>G (n.*7641C>G) c.1112C>G (p.Ala371Gly) c.519C>G c.7736C>G (p.Ala2579Gly) c.7541C>G (p.Ala2514Gly) c.7709C>G (p.Ala2570Gly) | |
| 16 | g.89268632G>T | CA397145297 | ANKRD11 | c.7838C>A (p.Ala2613Asp) c.*7641C>A (n.*7641C>A) c.1112C>A (p.Ala371Asp) c.519C>A c.7736C>A (p.Ala2579Asp) c.7541C>A (p.Ala2514Asp) c.7709C>A (p.Ala2570Asp) | |
| 16 | g.89268633C>A | CA397145299 | ANKRD11 | c.7837G>T (p.Ala2613Ser) c.*7640G>T (n.*7640G>T) c.1111G>T (p.Ala371Ser) c.518G>T c.7735G>T (p.Ala2579Ser) c.7540G>T (p.Ala2514Ser) c.7708G>T (p.Ala2570Ser) | gnomAD v4 |
| 16 | g.89268633C>G | CA397145301 | ANKRD11 | c.7837G>C (p.Ala2613Pro) c.*7640G>C (n.*7640G>C) c.1111G>C (p.Ala371Pro) c.518G>C c.7735G>C (p.Ala2579Pro) c.7540G>C (p.Ala2514Pro) c.7708G>C (p.Ala2570Pro) | |
| 16 | g.89268633C>T | CA397145298 | ANKRD11 | c.7837G>A (p.Ala2613Thr) c.*7640G>A (n.*7640G>A) c.1111G>A (p.Ala371Thr) c.518G>A c.7735G>A (p.Ala2579Thr) c.7540G>A (p.Ala2514Thr) c.7708G>A (p.Ala2570Thr) | |
| 16 | g.89268634C>A | CA397145305 | ANKRD11 | c.7836G>T (p.Glu2612Asp) c.*7639G>T (n.*7639G>T) c.1110G>T (p.Glu370Asp) c.517G>T c.7734G>T (p.Glu2578Asp) c.7539G>T (p.Glu2513Asp) c.7707G>T (p.Glu2569Asp) | gnomAD v4 |
| 16 | g.89268634C= | CA2241594818 | ANKRD11 | c.7836G= (p.Glu2612=) c.*7639G= (n.*7639G=) c.1110G= (p.Glu370=) c.517G= c.7734G= (p.Glu2578=) c.7539G= (p.Glu2513=) c.7707G= (p.Glu2569=) | |
| 16 | g.89268634C>G | CA397145303 | ANKRD11 | c.7836G>C (p.Glu2612Asp) c.*7639G>C (n.*7639G>C) c.1110G>C (p.Glu370Asp) c.517G>C c.7734G>C (p.Glu2578Asp) c.7539G>C (p.Glu2513Asp) c.7707G>C (p.Glu2569Asp) | |
| 16 | g.89268634C>T | CA497165703 | ANKRD11 | c.7836G>A (p.Glu2612=) c.*7639G>A (n.*7639G>A) c.1110G>A (p.Glu370=) c.517G>A c.7734G>A (p.Glu2578=) c.7539G>A (p.Glu2513=) c.7707G>A (p.Glu2569=) | dbSNP gnomAD v2 gnomAD v4 |
| 16 | g.89268635T>A | CA397145306 | ANKRD11 | c.7835A>T (p.Glu2612Val) c.*7638A>T (n.*7638A>T) c.1109A>T (p.Glu370Val) c.516A>T c.7733A>T (p.Glu2578Val) c.7538A>T (p.Glu2513Val) c.7706A>T (p.Glu2569Val) | gnomAD v4 |
| 16 | g.89268635T>C | CA397145308 | ANKRD11 | c.7835A>G (p.Glu2612Gly) c.*7638A>G (n.*7638A>G) c.1109A>G (p.Glu370Gly) c.516A>G c.7733A>G (p.Glu2578Gly) c.7538A>G (p.Glu2513Gly) c.7706A>G (p.Glu2569Gly) | |
| 16 | g.89268635T>G | CA397145309 | ANKRD11 | c.7835A>C (p.Glu2612Ala) c.*7638A>C (n.*7638A>C) c.1109A>C (p.Glu370Ala) c.516A>C c.7733A>C (p.Glu2578Ala) c.7538A>C (p.Glu2513Ala) c.7706A>C (p.Glu2569Ala) | |
| 16 | g.89268636C>A | CA397145310 | ANKRD11 | c.7834G>T (p.Glu2612Ter) c.*7637G>T (n.*7637G>T) c.1108G>T (p.Glu370Ter) c.515G>T c.7732G>T (p.Glu2578Ter) c.7537G>T (p.Glu2513Ter) c.7705G>T (p.Glu2569Ter) | gnomAD v4 |
| 16 | g.89268636C>G | CA397145311 | ANKRD11 | c.7834G>C (p.Glu2612Gln) c.*7637G>C (n.*7637G>C) c.1108G>C (p.Glu370Gln) c.515G>C c.7732G>C (p.Glu2578Gln) c.7537G>C (p.Glu2513Gln) c.7705G>C (p.Glu2569Gln) | |
| 16 | g.89268636C>T | CA397145313 | ANKRD11 | c.7834G>A (p.Glu2612Lys) c.*7637G>A (n.*7637G>A) c.1108G>A (p.Glu370Lys) c.515G>A c.7732G>A (p.Glu2578Lys) c.7537G>A (p.Glu2513Lys) c.7705G>A (p.Glu2569Lys) | gnomAD v4 COSMIC |
| 16 | g.89268637G>A | CA8240982 | ANKRD11 | c.7833C>T (p.His2611=) c.*7636C>T (n.*7636C>T) c.1107C>T (p.His369=) c.514C>T c.7731C>T (p.His2577=) c.7536C>T (p.His2512=) c.7704C>T (p.His2568=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 16 | g.89268637G>C | CA397145316 | ANKRD11 | c.7833C>G (p.His2611Gln) c.*7636C>G (n.*7636C>G) c.1107C>G (p.His369Gln) c.514C>G c.7731C>G (p.His2577Gln) c.7536C>G (p.His2512Gln) c.7704C>G (p.His2568Gln) | |
| 16 | g.89268637G= | CA2241594819 | ANKRD11 | c.7833C= (p.His2611=) c.*7636C= (n.*7636C=) c.1107C= (p.His369=) c.514C= c.7731C= (p.His2577=) c.7536C= (p.His2512=) c.7704C= (p.His2568=) | |
| 16 | g.89268637G>T | CA397145318 | ANKRD11 | c.7833C>A (p.His2611Gln) c.*7636C>A (n.*7636C>A) c.1107C>A (p.His369Gln) c.514C>A c.7731C>A (p.His2577Gln) c.7536C>A (p.His2512Gln) c.7704C>A (p.His2568Gln) | gnomAD v4 |
| 16 | g.89268638T>A | CA397145320 | ANKRD11 | c.7832A>T (p.His2611Leu) c.*7635A>T (n.*7635A>T) c.1106A>T (p.His369Leu) c.513A>T c.7730A>T (p.His2577Leu) c.7535A>T (p.His2512Leu) c.7703A>T (p.His2568Leu) | |
| 16 | g.89268638T>C | CA397145322 | ANKRD11 | c.7832A>G (p.His2611Arg) c.*7635A>G (n.*7635A>G) c.1106A>G (p.His369Arg) c.513A>G c.7730A>G (p.His2577Arg) c.7535A>G (p.His2512Arg) c.7703A>G (p.His2568Arg) | gnomAD v4 |
| 16 | g.89268638T>G | CA397145324 | ANKRD11 | c.7832A>C (p.His2611Pro) c.*7635A>C (n.*7635A>C) c.1106A>C (p.His369Pro) c.513A>C c.7730A>C (p.His2577Pro) c.7535A>C (p.His2512Pro) c.7703A>C (p.His2568Pro) | |
| 16 | g.89268639G>A | CA397145326 | ANKRD11 | c.7831C>T (p.His2611Tyr) c.*7634C>T (n.*7634C>T) c.1105C>T (p.His369Tyr) c.512C>T c.7729C>T (p.His2577Tyr) c.7534C>T (p.His2512Tyr) c.7702C>T (p.His2568Tyr) | gnomAD v4 COSMIC |
| 16 | g.89268639G>C | CA397145329 | ANKRD11 | c.7831C>G (p.His2611Asp) c.*7634C>G (n.*7634C>G) c.1105C>G (p.His369Asp) c.512C>G c.7729C>G (p.His2577Asp) c.7534C>G (p.His2512Asp) c.7702C>G (p.His2568Asp) | |
| 16 | g.89268639G>T | CA397145327 | ANKRD11 | c.7831C>A (p.His2611Asn) c.*7634C>A (n.*7634C>A) c.1105C>A (p.His369Asn) c.512C>A c.7729C>A (p.His2577Asn) c.7534C>A (p.His2512Asn) c.7702C>A (p.His2568Asn) | gnomAD v4 |
| 16 | g.89268640C>A | CA397145331 | ANKRD11 | c.7830G>T (p.Gln2610His) c.*7633G>T (n.*7633G>T) c.1104G>T (p.Gln368His) c.511G>T c.7728G>T (p.Gln2576His) c.7533G>T (p.Gln2511His) c.7701G>T (p.Gln2567His) | gnomAD v4 |
| 16 | g.89268640C>G | CA397145333 | ANKRD11 | c.7830G>C (p.Gln2610His) c.*7633G>C (n.*7633G>C) c.1104G>C (p.Gln368His) c.511G>C c.7728G>C (p.Gln2576His) c.7533G>C (p.Gln2511His) c.7701G>C (p.Gln2567His) | |
| 16 | g.89268640C>T | CA497165711 | ANKRD11 | c.7830G>A (p.Gln2610=) c.*7633G>A (n.*7633G>A) c.1104G>A (p.Gln368=) c.511G>A c.7728G>A (p.Gln2576=) c.7533G>A (p.Gln2511=) c.7701G>A (p.Gln2567=) | gnomAD v4 |
| 16 | g.89268641T>A | CA397145335 | ANKRD11 | c.7829A>T (p.Gln2610Leu) c.*7632A>T (n.*7632A>T) c.1103A>T (p.Gln368Leu) c.510A>T c.7727A>T (p.Gln2576Leu) c.7532A>T (p.Gln2511Leu) c.7700A>T (p.Gln2567Leu) | |
| 16 | g.89268641T>C | CA397145337 | ANKRD11 | c.7829A>G (p.Gln2610Arg) c.*7632A>G (n.*7632A>G) c.1103A>G (p.Gln368Arg) c.510A>G c.7727A>G (p.Gln2576Arg) c.7532A>G (p.Gln2511Arg) c.7700A>G (p.Gln2567Arg) | gnomAD v4 |
| 16 | g.89268641T>G | CA397145338 | ANKRD11 | c.7829A>C (p.Gln2610Pro) c.*7632A>C (n.*7632A>C) c.1103A>C (p.Gln368Pro) c.510A>C c.7727A>C (p.Gln2576Pro) c.7532A>C (p.Gln2511Pro) c.7700A>C (p.Gln2567Pro) | |
| 16 | g.89268642G>A | CA397145340 | ANKRD11 | c.7828C>T (p.Gln2610Ter) c.*7631C>T (n.*7631C>T) c.1102C>T (p.Gln368Ter) c.509C>T c.7726C>T (p.Gln2576Ter) c.7531C>T (p.Gln2511Ter) c.7699C>T (p.Gln2567Ter) | gnomAD v4 |
| 16 | g.89268642G>C | CA397145342 | ANKRD11 | c.7828C>G (p.Gln2610Glu) c.*7631C>G (n.*7631C>G) c.1102C>G (p.Gln368Glu) c.509C>G c.7726C>G (p.Gln2576Glu) c.7531C>G (p.Gln2511Glu) c.7699C>G (p.Gln2567Glu) | |
| 16 | g.89268642G>T | CA397145344 | ANKRD11 | c.7828C>A (p.Gln2610Lys) c.*7631C>A (n.*7631C>A) c.1102C>A (p.Gln368Lys) c.509C>A c.7726C>A (p.Gln2576Lys) c.7531C>A (p.Gln2511Lys) c.7699C>A (p.Gln2567Lys) | gnomAD v4 |
| 16 | g.89268643C>A | CA397145346 | ANKRD11 | c.7827G>T (p.Gln2609His) c.*7630G>T (n.*7630G>T) c.1101G>T (p.Gln367His) c.508G>T c.7725G>T (p.Gln2575His) c.7530G>T (p.Gln2510His) c.7698G>T (p.Gln2566His) | gnomAD v4 |
| 16 | g.89268643C>G | CA397145347 | ANKRD11 | c.7827G>C (p.Gln2609His) c.*7630G>C (n.*7630G>C) c.1101G>C (p.Gln367His) c.508G>C c.7725G>C (p.Gln2575His) c.7530G>C (p.Gln2510His) c.7698G>C (p.Gln2566His) | |
| 16 | g.89268643C>T | CA497165715 | ANKRD11 | c.7827G>A (p.Gln2609=) c.*7630G>A (n.*7630G>A) c.1101G>A (p.Gln367=) c.508G>A c.7725G>A (p.Gln2575=) c.7530G>A (p.Gln2510=) c.7698G>A (p.Gln2566=) | gnomAD v4 |
| 16 | g.89268644T>A | CA397145351 | ANKRD11 | c.7826A>T (p.Gln2609Leu) c.*7629A>T (n.*7629A>T) c.1100A>T (p.Gln367Leu) c.507A>T c.7724A>T (p.Gln2575Leu) c.7529A>T (p.Gln2510Leu) c.7697A>T (p.Gln2566Leu) | |
| 16 | g.89268644T>C | CA397145353 | ANKRD11 | c.7826A>G (p.Gln2609Arg) c.*7629A>G (n.*7629A>G) c.1100A>G (p.Gln367Arg) c.507A>G c.7724A>G (p.Gln2575Arg) c.7529A>G (p.Gln2510Arg) c.7697A>G (p.Gln2566Arg) | |
| 16 | g.89268644T>G | CA397145349 | ANKRD11 | c.7826A>C (p.Gln2609Pro) c.*7629A>C (n.*7629A>C) c.1100A>C (p.Gln367Pro) c.507A>C c.7724A>C (p.Gln2575Pro) c.7529A>C (p.Gln2510Pro) c.7697A>C (p.Gln2566Pro) | |
| 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 |