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 |
|---|---|---|---|---|---|
| 14 | g.28768450_28768467del | CA2624400295 | FOXG1 | c.1171_1188del (p.Gly391_Cys396del) | gnomAD v4 |
| 14 | g.28768450G>A | CA389476690 | FOXG1 | c.1171G>A (p.Gly391Ser) | |
| 14 | g.28768450G>C | CA389476688 | FOXG1 | c.1171G>C (p.Gly391Arg) | |
| 14 | g.28768450G>T | CA389476689 | FOXG1 | c.1171G>T (p.Gly391Cys) | |
| 14 | g.28768451G>A | CA389476691 | FOXG1 | c.1172G>A (p.Gly391Asp) | dbSNP |
| 14 | g.28768451G>C | CA389476692 | FOXG1 | c.1172G>C (p.Gly391Ala) | |
| 14 | g.28768451G= | CA2126000421 | FOXG1 | c.1172G= (p.Gly391=) | |
| 14 | g.28768451G>T | CA389476693 | FOXG1 | c.1172G>T (p.Gly391Val) | dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.28768452C>A | CA486098377 | FOXG1 | c.1173C>A (p.Gly391=) | |
| 14 | g.28768452C= | CA2126000422 | FOXG1 | c.1173C= (p.Gly391=) | |
| 14 | g.28768452C>G | CA486098378 | FOXG1 | c.1173C>G (p.Gly391=) | |
| 14 | g.28768452C>T | CA486098379 | FOXG1 | c.1173C>T (p.Gly391=) | ClinVar dbSNP gnomAD v4 |
| 14 | g.28768453C>A | CA389476694 | FOXG1 | c.1174C>A (p.Leu392Met) | COSMIC |
| 14 | g.28768453C= | CA2126000423 | FOXG1 | c.1174C= (p.Leu392=) | |
| 14 | g.28768453C>G | CA389476695 | FOXG1 | c.1174C>G (p.Leu392Val) | |
| 14 | g.28768453C>T | CA486098380 | FOXG1 | c.1174C>T (p.Leu392=) | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.28768454T>A | CA389476698 | FOXG1 | c.1175T>A (p.Leu392Gln) | |
| 14 | g.28768454T>C | CA389476697 | FOXG1 | c.1175T>C (p.Leu392Pro) | |
| 14 | g.28768454T>G | CA389476696 | FOXG1 | c.1175T>G (p.Leu392Arg) | |
| 14 | g.28768455G>A | CA486098381 | FOXG1 | c.1176G>A (p.Leu392=) | gnomAD v4 |
| 14 | g.28768455G>C | CA486098385 | FOXG1 | c.1176G>C (p.Leu392=) | |
| 14 | g.28768455G>T | CA486098383 | FOXG1 | c.1176G>T (p.Leu392=) | |
| 14 | g.28768456T>A | CA389476699 | FOXG1 | c.1177T>A (p.Ser393Thr) | |
| 14 | g.28768456T>C | CA389476700 | FOXG1 | c.1177T>C (p.Ser393Pro) | |
| 14 | g.28768456T>G | CA389476701 | FOXG1 | c.1177T>G (p.Ser393Ala) | |
| 14 | g.28768457C>A | CA389476702 | FOXG1 | c.1178C>A (p.Ser393Ter) | |
| 14 | g.28768457C= | CA2126000424 | FOXG1 | c.1178C= (p.Ser393=) | |
| 14 | g.28768457C>G | CA389476703 | FOXG1 | c.1178C>G (p.Ser393Trp) | ClinVar dbSNP |
| 14 | g.28768457C>T | CA389476704 | FOXG1 | c.1178C>T (p.Ser393Leu) | |
| 14 | g.28768458G>A | CA486098387 | FOXG1 | c.1179G>A (p.Ser393=) | |
| 14 | g.28768458G>C | CA486098388 | FOXG1 | c.1179G>C (p.Ser393=) | ClinVar dbSNP |
| 14 | g.28768458G>T | CA486098390 | FOXG1 | c.1179G>T (p.Ser393=) | |
| 14 | g.28768459G>A | CA389476705 | FOXG1 | c.1180G>A (p.Val394Met) | |
| 14 | g.28768459G>C | CA389476706 | FOXG1 | c.1180G>C (p.Val394Leu) | |
| 14 | g.28768459G>T | CA389476707 | FOXG1 | c.1180G>T (p.Val394Leu) | |
| 14 | g.28768460T>A | CA389476708 | FOXG1 | c.1181T>A (p.Val394Glu) | |
| 14 | g.28768460T>C | CA389476709 | FOXG1 | c.1181T>C (p.Val394Ala) | |
| 14 | g.28768460T>G | CA389476710 | FOXG1 | c.1181T>G (p.Val394Gly) | ClinVar dbSNP gnomAD v4 |
| 14 | g.28768460T= | CA2126000425 | FOXG1 | c.1181T= (p.Val394=) | |
| 14 | g.28768461G>A | CA486098393 | FOXG1 | c.1182G>A (p.Val394=) | dbSNP gnomAD v4 |
| 14 | g.28768461G>C | CA486098394 | FOXG1 | c.1182G>C (p.Val394=) | |
| 14 | g.28768461G= | CA2126000426 | FOXG1 | c.1182G= (p.Val394=) | |
| 14 | g.28768461G>T | CA7140668 | FOXG1 | c.1182G>T (p.Val394=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.28768462C>A | CA389476713 | FOXG1 | c.1183C>A (p.Pro395Thr) | |
| 14 | g.28768462C>G | CA389476711 | FOXG1 | c.1183C>G (p.Pro395Ala) | |
| 14 | g.28768462C>T | CA389476712 | FOXG1 | c.1183C>T (p.Pro395Ser) | gnomAD v4 |
| 14 | g.28768463C>A | CA389476714 | FOXG1 | c.1184C>A (p.Pro395His) | |
| 14 | g.28768463C= | CA2126000427 | FOXG1 | c.1184C= (p.Pro395=) | |
| 14 | g.28768463C>G | CA389476715 | FOXG1 | c.1184C>G (p.Pro395Arg) | |
| 14 | g.28768463C>T | CA389476716 | FOXG1 | c.1184C>T (p.Pro395Leu) | dbSNP gnomAD v2 |
| 14 | g.28768464C>A | CA486098397 | FOXG1 | c.1185C>A (p.Pro395=) | |
| 14 | g.28768464C= | CA2126000428 | FOXG1 | c.1185C= (p.Pro395=) | |
| 14 | g.28768464C>G | CA486098398 | FOXG1 | c.1185C>G (p.Pro395=) | gnomAD v4 |
| 14 | g.28768464C>T | CA486098399 | FOXG1 | c.1185C>T (p.Pro395=) | dbSNP |
| 14 | g.28768465T>A | CA389476717 | FOXG1 | c.1186T>A (p.Cys396Ser) | ClinVar dbSNP |
| 14 | g.28768465T>C | CA389476718 | FOXG1 | c.1186T>C (p.Cys396Arg) | |
| 14 | g.28768465T>G | CA389476719 | FOXG1 | c.1186T>G (p.Cys396Gly) | |
| 14 | g.28768465T= | CA2126000429 | FOXG1 | c.1186T= (p.Cys396=) | |
| 14 | g.28768466G>A | CA389476720 | FOXG1 | c.1187G>A (p.Cys396Tyr) | gnomAD v4 |
| 14 | g.28768466G>C | CA389476721 | FOXG1 | c.1187G>C (p.Cys396Ser) | |
| 14 | g.28768466G>T | CA389476722 | FOXG1 | c.1187G>T (p.Cys396Phe) | |
| 14 | g.28768467C>A | CA389476723 | FOXG1 | c.1188C>A (p.Cys396Ter) | |
| 14 | g.28768467C= | CA2126000430 | FOXG1 | c.1188C= (p.Cys396=) | |
| 14 | g.28768467C>G | CA389476724 | FOXG1 | c.1188C>G (p.Cys396Trp) | |
| 14 | g.28768467C>T | CA7140669 | FOXG1 | c.1188C>T (p.Cys396=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.28768468T>A | CA389476727 | FOXG1 | c.1189T>A (p.Ser397Thr) | |
| 14 | g.28768468T>C | CA389476726 | FOXG1 | c.1189T>C (p.Ser397Pro) | |
| 14 | g.28768468T>G | CA389476725 | FOXG1 | c.1189T>G (p.Ser397Ala) | |
| 14 | g.28768469C>A | CA389476728 | FOXG1 | c.1190C>A (p.Ser397Tyr) | |
| 14 | g.28768469C= | CA2126000431 | FOXG1 | c.1190C= (p.Ser397=) | |
| 14 | g.28768469C>G | CA389476729 | FOXG1 | c.1190C>G (p.Ser397Cys) | |
| 14 | g.28768469C>T | CA16607642 | FOXG1 | c.1190C>T (p.Ser397Phe) | ClinVar dbSNP |
| 14 | g.28768470T>A | CA486098405 | FOXG1 | c.1191T>A (p.Ser397=) | |
| 14 | g.28768470T>C | CA486098406 | FOXG1 | c.1191T>C (p.Ser397=) | dbSNP gnomAD v2 COSMIC |
| 14 | g.28768470T>G | CA486098407 | FOXG1 | c.1191T>G (p.Ser397=) | |
| 14 | g.28768470T= | CA2126000432 | FOXG1 | c.1191T= (p.Ser397=) | |
| 14 | g.28768471G>A | CA389476730 | FOXG1 | c.1192G>A (p.Gly398Arg) | |
| 14 | g.28768471G>C | CA389476732 | FOXG1 | c.1192G>C (p.Gly398Arg) | |
| 14 | g.28768471G>T | CA389476731 | FOXG1 | c.1192G>T (p.Gly398Trp) | |
| 14 | g.28768472G>A | CA389476733 | FOXG1 | c.1193G>A (p.Gly398Glu) | |
| 14 | g.28768472G>C | CA389476734 | FOXG1 | c.1193G>C (p.Gly398Ala) | dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.28768472G= | CA2126000433 | FOXG1 | c.1193G= (p.Gly398=) | |
| 14 | g.28768472G>T | CA389476735 | FOXG1 | c.1193G>T (p.Gly398Val) | |
| 14 | g.28768473G>A | CA486098409 | FOXG1 | c.1194G>A (p.Gly398=) | gnomAD v4 |
| 14 | g.28768473G>C | CA486098410 | FOXG1 | c.1194G>C (p.Gly398=) | |
| 14 | g.28768473G>T | CA486098411 | FOXG1 | c.1194G>T (p.Gly398=) | |
| 14 | g.28768474A= | CA2126000434 | FOXG1 | c.1195A= (p.Thr399=) | |
| 14 | g.28768474A>C | CA389476736 | FOXG1 | c.1195A>C (p.Thr399Pro) | |
| 14 | g.28768474A>G | CA389476737 | FOXG1 | c.1195A>G (p.Thr399Ala) | |
| 14 | g.28768474A>T | CA7140670 | FOXG1 | c.1195A>T (p.Thr399Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.28768475C>A | CA389476738 | FOXG1 | c.1196C>A (p.Thr399Asn) | |
| 14 | g.28768475C>G | CA389476739 | FOXG1 | c.1196C>G (p.Thr399Ser) | |
| 14 | g.28768475C>T | CA389476740 | FOXG1 | c.1196C>T (p.Thr399Ile) | |
| 14 | g.28768476C>A | CA486098415 | FOXG1 | c.1197C>A (p.Thr399=) | |
| 14 | g.28768476C>G | CA486098413 | FOXG1 | c.1197C>G (p.Thr399=) | |
| 14 | g.28768476C>T | CA486098414 | FOXG1 | c.1197C>T (p.Thr399=) | gnomAD v4 |
| 14 | g.28768477T>A | CA389476741 | FOXG1 | c.1198T>A (p.Tyr400Asn) | |
| 14 | g.28768477T>C | CA389476742 | FOXG1 | c.1198T>C (p.Tyr400His) | |
| 14 | g.28768477T>G | CA389476743 | FOXG1 | c.1198T>G (p.Tyr400Asp) | |
| 14 | g.28768478A>C | CA389476746 | FOXG1 | c.1199A>C (p.Tyr400Ser) | |
| 14 | g.28768478A>G | CA389476745 | FOXG1 | c.1199A>G (p.Tyr400Cys) | |
| 14 | g.28768478A>T | CA389476744 | FOXG1 | c.1199A>T (p.Tyr400Phe) | |
| 14 | g.28768479C>A | CA235611 | FOXG1 | c.1200C>A (p.Tyr400Ter) | ClinVar dbSNP |
| 14 | g.28768479C= | CA2126000435 | FOXG1 | c.1200C= (p.Tyr400=) | |
| 14 | g.28768479C>G | CA123557 | FOXG1 | c.1200C>G (p.Tyr400Ter) | ClinVar dbSNP |
| 14 | g.28768479C>T | CA7140671 | FOXG1 | c.1200C>T (p.Tyr400=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28768480T>A | CA389476747 | FOXG1 | c.1201T>A (p.Ser401Thr) | |
| 14 | g.28768480T>C | CA389476748 | FOXG1 | c.1201T>C (p.Ser401Pro) | |
| 14 | g.28768480T>G | CA389476749 | FOXG1 | c.1201T>G (p.Ser401Ala) | |
| 14 | g.28768481C>A | CA389476750 | FOXG1 | c.1202C>A (p.Ser401Tyr) | |
| 14 | g.28768481C>G | CA389476751 | FOXG1 | c.1202C>G (p.Ser401Cys) | |
| 14 | g.28768481C>T | CA389476752 | FOXG1 | c.1202C>T (p.Ser401Phe) | COSMIC |
| 14 | g.28768482C>A | CA486098418 | FOXG1 | c.1203C>A (p.Ser401=) | |
| 14 | g.28768482C= | CA2126000436 | FOXG1 | c.1203C= (p.Ser401=) | |
| 14 | g.28768482C>G | CA486098422 | FOXG1 | c.1203C>G (p.Ser401=) | |
| 14 | g.28768482C>T | CA7140672 | FOXG1 | c.1203C>T (p.Ser401=) | ClinVar dbSNP ExAC gnomAD v3 gnomAD v4 |
| 14 | g.28768483C>A | CA389476753 | FOXG1 | c.1204C>A (p.Leu402Ile) | |
| 14 | g.28768483C>G | CA389476754 | FOXG1 | c.1204C>G (p.Leu402Val) | |
| 14 | g.28768483C>T | CA389476755 | FOXG1 | c.1204C>T (p.Leu402Phe) | COSMIC |
| 14 | g.28768484T>A | CA389476757 | FOXG1 | c.1205T>A (p.Leu402His) | |
| 14 | g.28768484T>C | CA389476758 | FOXG1 | c.1205T>C (p.Leu402Pro) | |
| 14 | g.28768484T>G | CA389476756 | FOXG1 | c.1205T>G (p.Leu402Arg) | |
| 14 | g.28768485C>A | CA486098424 | FOXG1 | c.1206C>A (p.Leu402=) | |
| 14 | g.28768485C= | CA2126000437 | FOXG1 | c.1206C= (p.Leu402=) | |
| 14 | g.28768485C>G | CA486098425 | FOXG1 | c.1206C>G (p.Leu402=) | |
| 14 | g.28768485C>T | CA486098426 | FOXG1 | c.1206C>T (p.Leu402=) | dbSNP |
| 14 | g.28768486A>C | CA389476759 | FOXG1 | c.1207A>C (p.Asn403His) | |
| 14 | g.28768486A>G | CA389476760 | FOXG1 | c.1207A>G (p.Asn403Asp) | |
| 14 | g.28768486A>T | CA389476761 | FOXG1 | c.1207A>T (p.Asn403Tyr) | |
| 14 | g.28768487A= | CA2126000438 | FOXG1 | c.1208A= (p.Asn403=) | |
| 14 | g.28768487A>C | CA389476762 | FOXG1 | c.1208A>C (p.Asn403Thr) | |
| 14 | g.28768487A>G | CA258396598 | FOXG1 | c.1208A>G (p.Asn403Ser) | ClinVar dbSNP gnomAD v4 |
| 14 | g.28768487A>T | CA389476763 | FOXG1 | c.1208A>T (p.Asn403Ile) | |
| 14 | g.28768488C>A | CA389476764 | FOXG1 | c.1209C>A (p.Asn403Lys) | |
| 14 | g.28768488C>G | CA389476765 | FOXG1 | c.1209C>G (p.Asn403Lys) | |
| 14 | g.28768488C>T | CA486098431 | FOXG1 | c.1209C>T (p.Asn403=) | |
| 14 | g.28768489C>A | CA389476766 | FOXG1 | c.1210C>A (p.Pro404Thr) | |
| 14 | g.28768489C>G | CA389476767 | FOXG1 | c.1210C>G (p.Pro404Ala) | |
| 14 | g.28768489C>T | CA389476768 | FOXG1 | c.1210C>T (p.Pro404Ser) | |
| 14 | g.28768490C>A | CA389476771 | FOXG1 | c.1211C>A (p.Pro404His) | |
| 14 | g.28768490C>G | CA389476769 | FOXG1 | c.1211C>G (p.Pro404Arg) | |
| 14 | g.28768490C>T | CA389476770 | FOXG1 | c.1211C>T (p.Pro404Leu) | |
| 14 | g.28768491C>A | CA486098434 | FOXG1 | c.1212C>A (p.Pro404=) | COSMIC |
| 14 | g.28768491C= | CA2126000439 | FOXG1 | c.1212C= (p.Pro404=) | |
| 14 | g.28768491C>G | CA486098435 | FOXG1 | c.1212C>G (p.Pro404=) | |
| 14 | g.28768491C>T | CA486098436 | FOXG1 | c.1212C>T (p.Pro404=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28768492T>A | CA389476772 | FOXG1 | c.1213T>A (p.Cys405Ser) | dbSNP |
| 14 | g.28768492T>C | CA389476773 | FOXG1 | c.1213T>C (p.Cys405Arg) | |
| 14 | g.28768492T>G | CA389476774 | FOXG1 | c.1213T>G (p.Cys405Gly) | |
| 14 | g.28768493G>A | CA389476775 | FOXG1 | c.1214G>A (p.Cys405Tyr) | |
| 14 | g.28768493G>C | CA389476776 | FOXG1 | c.1214G>C (p.Cys405Ser) | |
| 14 | g.28768493G>T | CA389476777 | FOXG1 | c.1214G>T (p.Cys405Phe) | ClinVar dbSNP |
| 14 | g.28768494C>A | CA389476778 | FOXG1 | c.1215C>A (p.Cys405Ter) | |
| 14 | g.28768494C>G | CA389476779 | FOXG1 | c.1215C>G (p.Cys405Trp) | |
| 14 | g.28768494C>T | CA486098438 | FOXG1 | c.1215C>T (p.Cys405=) | |
| 14 | g.28768495T>A | CA389476780 | FOXG1 | c.1216T>A (p.Ser406Thr) | |
| 14 | g.28768495T>C | CA389476781 | FOXG1 | c.1216T>C (p.Ser406Pro) | |
| 14 | g.28768495T>G | CA389476782 | FOXG1 | c.1216T>G (p.Ser406Ala) | |
| 14 | g.28768496C>A | CA389476784 | FOXG1 | c.1217C>A (p.Ser406Tyr) | |
| 14 | g.28768496C>G | CA389476785 | FOXG1 | c.1217C>G (p.Ser406Cys) | |
| 14 | g.28768496C>T | CA389476783 | FOXG1 | c.1217C>T (p.Ser406Phe) | |
| 14 | g.28768497C>A | CA486098440 | FOXG1 | c.1218C>A (p.Ser406=) | |
| 14 | g.28768497C= | CA2126000440 | FOXG1 | c.1218C= (p.Ser406=) | |
| 14 | g.28768497C>G | CA294772 | FOXG1 | c.1218C>G (p.Ser406=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28768497C>T | CA486098442 | FOXG1 | c.1218C>T (p.Ser406=) | dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.28768498G>A | CA389476786 | FOXG1 | c.1219G>A (p.Val407Ile) | dbSNP gnomAD v4 COSMIC |
| 14 | g.28768498G>C | CA389476787 | FOXG1 | c.1219G>C (p.Val407Leu) | ClinVar dbSNP |
| 14 | g.28768498G= | CA2126000441 | FOXG1 | c.1219G= (p.Val407=) | |
| 14 | g.28768498G>T | CA389476788 | FOXG1 | c.1219G>T (p.Val407Phe) | |
| 14 | g.28768499T>A | CA389476789 | FOXG1 | c.1220T>A (p.Val407Asp) | |
| 14 | g.28768499T>C | CA389476790 | FOXG1 | c.1220T>C (p.Val407Ala) | |
| 14 | g.28768499T>G | CA389476791 | FOXG1 | c.1220T>G (p.Val407Gly) | |
| 14 | g.28768500C>A | CA486098448 | FOXG1 | c.1221C>A (p.Val407=) | |
| 14 | g.28768500C= | CA2126000442 | FOXG1 | c.1221C= (p.Val407=) | |
| 14 | g.28768500C>G | CA486098449 | FOXG1 | c.1221C>G (p.Val407=) | dbSNP gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.28768500C>T | CA486098450 | FOXG1 | c.1221C>T (p.Val407=) | ClinVar |
| 14 | g.28768501A= | CA2126000443 | FOXG1 | c.1222A= (p.Asn408=) | |
| 14 | g.28768501A>C | CA389476792 | FOXG1 | c.1222A>C (p.Asn408His) | |
| 14 | g.28768501A>G | CA389476793 | FOXG1 | c.1222A>G (p.Asn408Asp) | |
| 14 | g.28768501A>T | CA389476794 | FOXG1 | c.1222A>T (p.Asn408Tyr) | ClinVar dbSNP |
| 14 | g.28768502A>C | CA389476795 | FOXG1 | c.1223A>C (p.Asn408Thr) | |
| 14 | g.28768502A>G | CA389476796 | FOXG1 | c.1223A>G (p.Asn408Ser) | ClinVar gnomAD v4 COSMIC |
| 14 | g.28768502A>T | CA389476797 | FOXG1 | c.1223A>T (p.Asn408Ile) | |
| 14 | g.28768503C>A | CA389476799 | FOXG1 | c.1224C>A (p.Asn408Lys) | |
| 14 | g.28768503C= | CA2126000444 | FOXG1 | c.1224C= (p.Asn408=) | |
| 14 | g.28768503C>G | CA389476798 | FOXG1 | c.1224C>G (p.Asn408Lys) | |
| 14 | g.28768503C>T | CA486098455 | FOXG1 | c.1224C>T (p.Asn408=) | ClinVar dbSNP |
| 14 | g.28768504C>A | CA389476800 | FOXG1 | c.1225C>A (p.Leu409Met) | |
| 14 | g.28768504C>G | CA389476801 | FOXG1 | c.1225C>G (p.Leu409Val) | |
| 14 | g.28768504C>T | CA486098458 | FOXG1 | c.1225C>T (p.Leu409=) | |
| 14 | g.28768505T>A | CA389476802 | FOXG1 | c.1226T>A (p.Leu409Gln) | |
| 14 | g.28768505T>C | CA389476803 | FOXG1 | c.1226T>C (p.Leu409Pro) | |
| 14 | g.28768505T>G | CA389476804 | FOXG1 | c.1226T>G (p.Leu409Arg) | |
| 14 | g.28768506G>A | CA486098459 | FOXG1 | c.1227G>A (p.Leu409=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.28768506G>C | CA486098460 | FOXG1 | c.1227G>C (p.Leu409=) | |
| 14 | g.28768506G= | CA2126000445 | FOXG1 | c.1227G= (p.Leu409=) | |
| 14 | g.28768506G>T | CA486098461 | FOXG1 | c.1227G>T (p.Leu409=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.28768507C>A | CA389476807 | FOXG1 | c.1228C>A (p.Leu410Ile) | |
| 14 | g.28768507C>G | CA389476806 | FOXG1 | c.1228C>G (p.Leu410Val) | |
| 14 | g.28768507C>T | CA389476805 | FOXG1 | c.1228C>T (p.Leu410Phe) | |
| 14 | g.28768508T>A | CA389476808 | FOXG1 | c.1229T>A (p.Leu410His) | |
| 14 | g.28768508T>C | CA389476809 | FOXG1 | c.1229T>C (p.Leu410Pro) | |
| 14 | g.28768508T>G | CA389476810 | FOXG1 | c.1229T>G (p.Leu410Arg) | COSMIC |
| 14 | g.28768509C>A | CA486098468 | FOXG1 | c.1230C>A (p.Leu410=) | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.28768509C= | CA2126000446 | FOXG1 | c.1230C= (p.Leu410=) | |
| 14 | g.28768509C>G | CA486098471 | FOXG1 | c.1230C>G (p.Leu410=) | |
| 14 | g.28768509C>T | CA486098469 | FOXG1 | c.1230C>T (p.Leu410=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.28768510G>A | CA389476811 | FOXG1 | c.1231G>A (p.Ala411Thr) | |
| 14 | g.28768510G>C | CA389476812 | FOXG1 | c.1231G>C (p.Ala411Pro) | |
| 14 | g.28768510G>T | CA389476813 | FOXG1 | c.1231G>T (p.Ala411Ser) | |
| 14 | g.28768511C>A | CA389476814 | FOXG1 | c.1232C>A (p.Ala411Glu) | |
| 14 | g.28768511C>G | CA389476816 | FOXG1 | c.1232C>G (p.Ala411Gly) | |
| 14 | g.28768511C>T | CA389476815 | FOXG1 | c.1232C>T (p.Ala411Val) | COSMIC |
| 14 | g.28768512G>A | CA285651 | FOXG1 | c.1233G>A (p.Ala411=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28768512G>C | CA486098473 | FOXG1 | c.1233G>C (p.Ala411=) | |
| 14 | g.28768512G= | CA2126000447 | FOXG1 | c.1233G= (p.Ala411=) | |
| 14 | g.28768512G>T | CA486098474 | FOXG1 | c.1233G>T (p.Ala411=) | gnomAD v4 |
| 14 | g.28768513G>A | CA389476817 | FOXG1 | c.1234G>A (p.Gly412Ser) | |
| 14 | g.28768513G>C | CA389476818 | FOXG1 | c.1234G>C (p.Gly412Arg) | |
| 14 | g.28768513G>T | CA389476819 | FOXG1 | c.1234G>T (p.Gly412Cys) | COSMIC |
| 14 | g.28768514G>A | CA389476820 | FOXG1 | c.1235G>A (p.Gly412Asp) | ClinVar COSMIC |
| 14 | g.28768514G>C | CA389476821 | FOXG1 | c.1235G>C (p.Gly412Ala) | |
| 14 | g.28768514G>T | CA389476822 | FOXG1 | c.1235G>T (p.Gly412Val) | |
| 14 | g.28768515C>A | CA486098478 | FOXG1 | c.1236C>A (p.Gly412=) | |
| 14 | g.28768515C>G | CA486098479 | FOXG1 | c.1236C>G (p.Gly412=) | |
| 14 | g.28768515C>T | CA486098481 | FOXG1 | c.1236C>T (p.Gly412=) | |
| 14 | g.28768516C>A | CA389476823 | FOXG1 | c.1237C>A (p.Gln413Lys) | COSMIC |
| 14 | g.28768516C>G | CA389476824 | FOXG1 | c.1237C>G (p.Gln413Glu) | |
| 14 | g.28768516C>T | CA389476825 | FOXG1 | c.1237C>T (p.Gln413Ter) | |
| 14 | g.28768517A>C | CA389476826 | FOXG1 | c.1238A>C (p.Gln413Pro) | |
| 14 | g.28768517A>G | CA389476827 | FOXG1 | c.1238A>G (p.Gln413Arg) | |
| 14 | g.28768517A>T | CA389476828 | FOXG1 | c.1238A>T (p.Gln413Leu) | |
| 14 | g.28768518G>A | CA486098487 | FOXG1 | c.1239G>A (p.Gln413=) | |
| 14 | g.28768518G>C | CA389476830 | FOXG1 | c.1239G>C (p.Gln413His) | |
| 14 | g.28768518G>T | CA389476829 | FOXG1 | c.1239G>T (p.Gln413His) | |
| 14 | g.28768519A>C | CA389476831 | FOXG1 | c.1240A>C (p.Thr414Pro) | |
| 14 | g.28768519A>G | CA389476832 | FOXG1 | c.1240A>G (p.Thr414Ala) | COSMIC |
| 14 | g.28768519A>T | CA389476833 | FOXG1 | c.1240A>T (p.Thr414Ser) | |
| 14 | g.28768520C>A | CA389476834 | FOXG1 | c.1241C>A (p.Thr414Asn) | dbSNP |
| 14 | g.28768520C= | CA2126000448 | FOXG1 | c.1241C= (p.Thr414=) | |
| 14 | g.28768520C>G | CA389476835 | FOXG1 | c.1241C>G (p.Thr414Ser) | |
| 14 | g.28768520C>T | CA389476836 | FOXG1 | c.1241C>T (p.Thr414Ile) | |
| 14 | g.28768521C>A | CA486098491 | FOXG1 | c.1242C>A (p.Thr414=) | |
| 14 | g.28768521C= | CA2126000449 | FOXG1 | c.1242C= (p.Thr414=) | |
| 14 | g.28768521C>G | CA486098493 | FOXG1 | c.1242C>G (p.Thr414=) | |
| 14 | g.28768521C>T | CA7140673 | FOXG1 | c.1242C>T (p.Thr414=) | dbSNP ExAC gnomAD v2 |
| 14 | g.28768522A= | CA2126000450 | FOXG1 | c.1243A= (p.Ser415=) | |
| 14 | g.28768522A>C | CA389476837 | FOXG1 | c.1243A>C (p.Ser415Arg) | |
| 14 | g.28768522A>G | CA389476838 | FOXG1 | c.1243A>G (p.Ser415Gly) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28768522A>T | CA389476839 | FOXG1 | c.1243A>T (p.Ser415Cys) | |
| 14 | g.28768523G>A | CA389476840 | FOXG1 | c.1244G>A (p.Ser415Asn) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.28768523G>C | CA389476841 | FOXG1 | c.1244G>C (p.Ser415Thr) | |
| 14 | g.28768523G= | CA2126000451 | FOXG1 | c.1244G= (p.Ser415=) | |
| 14 | g.28768523G>T | CA389476842 | FOXG1 | c.1244G>T (p.Ser415Ile) | |
| 14 | g.28768523_28768524del | CA2739277848 | FOXG1 | c.1244_1245del (p.Ser415IlefsTer?) | ClinVar |
| 14 | g.28768524T>A | CA389476844 | FOXG1 | c.1245T>A (p.Ser415Arg) | |
| 14 | g.28768524T>C | CA486098500 | FOXG1 | c.1245T>C (p.Ser415=) | |
| 14 | g.28768524T>G | CA389476843 | FOXG1 | c.1245T>G (p.Ser415Arg) | |
| 14 | g.28768525T>A | CA389476845 | FOXG1 | c.1246T>A (p.Tyr416Asn) | |
| 14 | g.28768525T>C | CA389476847 | FOXG1 | c.1246T>C (p.Tyr416His) | |
| 14 | g.28768525T>G | CA389476846 | FOXG1 | c.1246T>G (p.Tyr416Asp) | |
| 14 | g.28768526A>C | CA389476848 | FOXG1 | c.1247A>C (p.Tyr416Ser) | ClinVar |
| 14 | g.28768526A>G | CA389476849 | FOXG1 | c.1247A>G (p.Tyr416Cys) | |
| 14 | g.28768526A>T | CA389476850 | FOXG1 | c.1247A>T (p.Tyr416Phe) | |
| 14 | g.28768527C>A | CA389476851 | FOXG1 | c.1248C>A (p.Tyr416Ter) | |
| 14 | g.28768527C= | CA2126000452 | FOXG1 | c.1248C= (p.Tyr416=) | |
| 14 | g.28768527C>G | CA199429 | FOXG1 | c.1248C>G (p.Tyr416Ter) | ClinVar dbSNP |
| 14 | g.28768527C>T | CA486098503 | FOXG1 | c.1248C>T (p.Tyr416=) | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.28768528T>A | CA389476852 | FOXG1 | c.1249T>A (p.Phe417Ile) | |
| 14 | g.28768528T>C | CA7140674 | FOXG1 | c.1249T>C (p.Phe417Leu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.28768528T>G | CA389476853 | FOXG1 | c.1249T>G (p.Phe417Val) | |
| 14 | g.28768528T= | CA2126000453 | FOXG1 | c.1249T= (p.Phe417=) | |
| 14 | g.28768529T>A | CA389476854 | FOXG1 | c.1250T>A (p.Phe417Tyr) | |
| 14 | g.28768529T>C | CA389476855 | FOXG1 | c.1250T>C (p.Phe417Ser) | |
| 14 | g.28768529T>G | CA389476856 | FOXG1 | c.1250T>G (p.Phe417Cys) | |
| 14 | g.28768530T>A | CA389476857 | FOXG1 | c.1251T>A (p.Phe417Leu) | |
| 14 | g.28768530T>C | CA486098506 | FOXG1 | c.1251T>C (p.Phe417=) | |
| 14 | g.28768530T>G | CA389476858 | FOXG1 | c.1251T>G (p.Phe417Leu) | |
| 14 | g.28768531T>A | CA389476861 | FOXG1 | c.1252T>A (p.Phe418Ile) | |
| 14 | g.28768531T>C | CA389476859 | FOXG1 | c.1252T>C (p.Phe418Leu) | |
| 14 | g.28768531T>G | CA389476860 | FOXG1 | c.1252T>G (p.Phe418Val) | |
| 14 | g.28768532T>A | CA389476862 | FOXG1 | c.1253T>A (p.Phe418Tyr) | |
| 14 | g.28768532T>C | CA389476863 | FOXG1 | c.1253T>C (p.Phe418Ser) | dbSNP |
| 14 | g.28768532T>G | CA389476864 | FOXG1 | c.1253T>G (p.Phe418Cys) | |
| 14 | g.28768532T= | CA2126000454 | FOXG1 | c.1253T= (p.Phe418=) | |
| 14 | g.28768534_28768553dup | CA2697553887 | FOXG1 | c.1255_1274dup (p.Met426ProfsTer8) | ClinVar |
| 14 | g.28768533C>A | CA389476865 | FOXG1 | c.1254C>A (p.Phe418Leu) | ClinVar dbSNP |
| 14 | g.28768533C= | CA2126000455 | FOXG1 | c.1254C= (p.Phe418=) | |
| 14 | g.28768533C>G | CA389476866 | FOXG1 | c.1254C>G (p.Phe418Leu) | |
| 14 | g.28768533C>T | CA7140675 | FOXG1 | c.1254C>T (p.Phe418=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.28768537del | CA645570799 | FOXG1 | c.1258del (p.His420ThrfsTer7) | COSMIC |
| 14 | g.28768534C>A | CA389476867 | FOXG1 | c.1255C>A (p.Pro419Thr) | |
| 14 | g.28768534C>G | CA389476868 | FOXG1 | c.1255C>G (p.Pro419Ala) | |
| 14 | g.28768534C>T | CA389476869 | FOXG1 | c.1255C>T (p.Pro419Ser) | ClinVar dbSNP |
| 14 | g.28768535C>A | CA389476870 | FOXG1 | c.1256C>A (p.Pro419His) | |
| 14 | g.28768535C= | CA2126000456 | FOXG1 | c.1256C= (p.Pro419=) | |
| 14 | g.28768535C>G | CA389476871 | FOXG1 | c.1256C>G (p.Pro419Arg) | |
| 14 | g.28768535C>T | CA389476872 | FOXG1 | c.1256C>T (p.Pro419Leu) | ClinVar dbSNP |
| 14 | g.28768536C>A | CA486098513 | FOXG1 | c.1257C>A (p.Pro419=) | |
| 14 | g.28768536C>G | CA486098516 | FOXG1 | c.1257C>G (p.Pro419=) | |
| 14 | g.28768536C>T | CA486098514 | FOXG1 | c.1257C>T (p.Pro419=) | ClinVar gnomAD v4 |
| 14 | g.28768537C>A | CA389476873 | FOXG1 | c.1258C>A (p.His420Asn) | |
| 14 | g.28768537C>G | CA389476875 | FOXG1 | c.1258C>G (p.His420Asp) | |
| 14 | g.28768537C>T | CA389476874 | FOXG1 | c.1258C>T (p.His420Tyr) | |
| 14 | g.28768538A>C | CA389476876 | FOXG1 | c.1259A>C (p.His420Pro) | |
| 14 | g.28768538A>G | CA389476877 | FOXG1 | c.1259A>G (p.His420Arg) | |
| 14 | g.28768538A>T | CA389476878 | FOXG1 | c.1259A>T (p.His420Leu) | |
| 14 | g.28768539C>A | CA389476879 | FOXG1 | c.1260C>A (p.His420Gln) | |
| 14 | g.28768539C= | CA2126000457 | FOXG1 | c.1260C= (p.His420=) | |
| 14 | g.28768539C>G | CA389476880 | FOXG1 | c.1260C>G (p.His420Gln) | gnomAD v4 |
| 14 | g.28768539C>T | CA486098523 | FOXG1 | c.1260C>T (p.His420=) | dbSNP gnomAD v4 |
| 14 | g.28768540G>A | CA389476881 | FOXG1 | c.1261G>A (p.Val421Ile) | gnomAD v4 |
| 14 | g.28768540G>C | CA389476882 | FOXG1 | c.1261G>C (p.Val421Leu) | dbSNP |
| 14 | g.28768540G= | CA2126000458 | FOXG1 | c.1261G= (p.Val421=) | |
| 14 | g.28768540G>T | CA389476883 | FOXG1 | c.1261G>T (p.Val421Phe) | |
| 14 | g.28768541T>A | CA389476884 | FOXG1 | c.1262T>A (p.Val421Asp) | |
| 14 | g.28768541T>C | CA389476885 | FOXG1 | c.1262T>C (p.Val421Ala) | |
| 14 | g.28768541T>G | CA389476886 | FOXG1 | c.1262T>G (p.Val421Gly) | |
| 14 | g.28768542C>A | CA486098526 | FOXG1 | c.1263C>A (p.Val421=) | |
| 14 | g.28768542C= | CA2126000459 | FOXG1 | c.1263C= (p.Val421=) | |
| 14 | g.28768542C>G | CA7140676 | FOXG1 | c.1263C>G (p.Val421=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28768542C>T | CA486098529 | FOXG1 | c.1263C>T (p.Val421=) | COSMIC |
| 14 | g.28768544del | CA2801003439 | FOXG1 | c.1265del (p.Pro422ArgfsTer5) | |
| 14 | g.28768543C>A | CA389476889 | FOXG1 | c.1264C>A (p.Pro422Thr) | |
| 14 | g.28768543C>G | CA389476887 | FOXG1 | c.1264C>G (p.Pro422Ala) | |
| 14 | g.28768543C>T | CA389476888 | FOXG1 | c.1264C>T (p.Pro422Ser) | COSMIC |
| 14 | g.28768544C>A | CA389476890 | FOXG1 | c.1265C>A (p.Pro422Gln) | |
| 14 | g.28768544C>G | CA389476891 | FOXG1 | c.1265C>G (p.Pro422Arg) | |
| 14 | g.28768544C>T | CA389476892 | FOXG1 | c.1265C>T (p.Pro422Leu) | gnomAD v4 COSMIC |
| 14 | g.28768545G>A | CA486098534 | FOXG1 | c.1266G>A (p.Pro422=) | dbSNP COSMIC |
| 14 | g.28768545G>C | CA486098536 | FOXG1 | c.1266G>C (p.Pro422=) | |
| 14 | g.28768545G= | CA2126000460 | FOXG1 | c.1266G= (p.Pro422=) | |
| 14 | g.28768545G>T | CA486098537 | FOXG1 | c.1266G>T (p.Pro422=) | gnomAD v4 |
| 14 | g.28768546C>A | CA389476893 | FOXG1 | c.1267C>A (p.His423Asn) | |
| 14 | g.28768546C>G | CA389476894 | FOXG1 | c.1267C>G (p.His423Asp) | |
| 14 | g.28768546C>T | CA389476895 | FOXG1 | c.1267C>T (p.His423Tyr) | |
| 14 | g.28768547A= | CA2126000461 | FOXG1 | c.1268A= (p.His423=) | |
| 14 | g.28768547A>C | CA389476896 | FOXG1 | c.1268A>C (p.His423Pro) | |
| 14 | g.28768547A>G | CA389476897 | FOXG1 | c.1268A>G (p.His423Arg) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28768547A>T | CA389476898 | FOXG1 | c.1268A>T (p.His423Leu) | |
| 14 | g.28768548C>A | CA389476899 | FOXG1 | c.1269C>A (p.His423Gln) | |
| 14 | g.28768548C>G | CA389476900 | FOXG1 | c.1269C>G (p.His423Gln) | |
| 14 | g.28768548C>T | CA486098548 | FOXG1 | c.1269C>T (p.His423=) | |
| 14 | g.28768549C>A | CA389476902 | FOXG1 | c.1270C>A (p.Pro424Thr) | |
| 14 | g.28768549C= | CA2126000462 | FOXG1 | c.1270C= (p.Pro424=) | |
| 14 | g.28768549C>G | CA389476903 | FOXG1 | c.1270C>G (p.Pro424Ala) | dbSNP gnomAD v4 |
| 14 | g.28768549C>T | CA389476901 | FOXG1 | c.1270C>T (p.Pro424Ser) | gnomAD v4 |
| 14 | g.28768550C>A | CA389476906 | FOXG1 | c.1271C>A (p.Pro424Gln) | dbSNP |
| 14 | g.28768550C>G | CA389476904 | FOXG1 | c.1271C>G (p.Pro424Arg) | |
| 14 | g.28768550C>T | CA389476905 | FOXG1 | c.1271C>T (p.Pro424Leu) |