14 | g.28768399_28768435del | CA2832528763 | FOXG1 | c.1120_1156del (p.Tyr374ProfsTer?)
| |
14 | g.28768434C>A | CA486098356 | FOXG1 | c.1155C>A (p.Ala385=)
| |
14 | g.28768434C= | CA2126000413 | FOXG1 | c.1155C= (p.Ala385=)
| |
14 | g.28768434C>G | CA486098357 | FOXG1 | c.1155C>G (p.Ala385=)
| |
14 | g.28768434C>T | CA486098355 | FOXG1 | c.1155C>T (p.Ala385=)
| ClinVar dbSNP COSMIC |
14 | g.28768435G>A | CA389476658 | FOXG1 | c.1156G>A (p.Ala386Thr)
| |
14 | g.28768435G>C | CA389476659 | FOXG1 | c.1156G>C (p.Ala386Pro)
| |
14 | g.28768435G>T | CA389476660 | FOXG1 | c.1156G>T (p.Ala386Ser)
| gnomAD v4 |
14 | g.28768436C>A | CA389476661 | FOXG1 | c.1157C>A (p.Ala386Asp)
| |
14 | g.28768436C>G | CA389476662 | FOXG1 | c.1157C>G (p.Ala386Gly)
| |
14 | g.28768436C>T | CA389476663 | FOXG1 | c.1157C>T (p.Ala386Val)
| COSMIC |
14 | g.28768437C>A | CA486098359 | FOXG1 | c.1158C>A (p.Ala386=)
| |
14 | g.28768437C= | CA2126000414 | FOXG1 | c.1158C= (p.Ala386=)
| |
14 | g.28768437C>G | CA7140667 | FOXG1 | c.1158C>G (p.Ala386=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.28768437C>T | CA7140666 | FOXG1 | c.1158C>T (p.Ala386=)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.28768438T>A | CA389476664 | FOXG1 | c.1159T>A (p.Ser387Thr)
| |
14 | g.28768438T>C | CA258396596 | FOXG1 | c.1159T>C (p.Ser387Pro)
| dbSNP |
14 | g.28768438T>G | CA389476665 | FOXG1 | c.1159T>G (p.Ser387Ala)
| |
14 | g.28768438T= | CA2126000415 | FOXG1 | c.1159T= (p.Ser387=)
| |
14 | g.28768438_28768440delinsTCG | CA2126000416 | FOXG1 | c.1159_1161delinsTCG (p.Ser387=)
| |
14 | g.28768450_28768467del | CA2624400295 | FOXG1 | c.1171_1188del (p.Gly391_Cys396del)
| gnomAD v4 |
14 | g.28768439del | CA2739291839 | FOXG1 | c.1160del (p.Ser387TrpfsTer?)
| |
14 | g.28768439C>A | CA389476667 | FOXG1 | c.1160C>A (p.Ser387Ter)
| |
14 | g.28768439C>G | CA389476668 | FOXG1 | c.1160C>G (p.Ser387Trp)
| |
14 | g.28768439C>T | CA389476666 | FOXG1 | c.1160C>T (p.Ser387Leu)
| |
14 | g.28768439_28768440delinsGTC | CA16042887 | FOXG1 | c.1160_1161delinsGTC (p.Ser387CysfsTer?)
| ClinVar dbSNP |
14 | g.28768440G>A | CA290949 | FOXG1 | c.1161G>A (p.Ser387=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.28768440G>C | CA486098362 | FOXG1 | c.1161G>C (p.Ser387=)
| ClinVar |
14 | g.28768440G= | CA2126000417 | FOXG1 | c.1161G= (p.Ser387=)
| |
14 | g.28768440G>T | CA486098365 | FOXG1 | c.1161G>T (p.Ser387=)
| ClinVar dbSNP |
14 | g.28768441G>A | CA389476669 | FOXG1 | c.1162G>A (p.Val388Met)
| gnomAD v4 |
14 | g.28768441G>C | CA389476670 | FOXG1 | c.1162G>C (p.Val388Leu)
| |
14 | g.28768441G>T | CA389476671 | FOXG1 | c.1162G>T (p.Val388Leu)
| |
14 | g.28768442T>A | CA389476672 | FOXG1 | c.1163T>A (p.Val388Glu)
| |
14 | g.28768442T>C | CA389476673 | FOXG1 | c.1163T>C (p.Val388Ala)
| |
14 | g.28768442T>G | CA389476674 | FOXG1 | c.1163T>G (p.Val388Gly)
| |
14 | g.28768443G>A | CA486098368 | FOXG1 | c.1164G>A (p.Val388=)
| gnomAD v4 |
14 | g.28768443G>C | CA486098369 | FOXG1 | c.1164G>C (p.Val388=)
| |
14 | g.28768443G>T | CA486098370 | FOXG1 | c.1164G>T (p.Val388=)
| |
14 | g.28768444C>A | CA389476675 | FOXG1 | c.1165C>A (p.Pro389Thr)
| |
14 | g.28768444C= | CA2126000418 | FOXG1 | c.1165C= (p.Pro389=)
| |
14 | g.28768444C>G | CA389476676 | FOXG1 | c.1165C>G (p.Pro389Ala)
| |
14 | g.28768444C>T | CA258396597 | FOXG1 | c.1165C>T (p.Pro389Ser)
| dbSNP gnomAD v3 gnomAD v4 |
14 | g.28768445C>A | CA389476677 | FOXG1 | c.1166C>A (p.Pro389His)
| |
14 | g.28768445C>G | CA389476678 | FOXG1 | c.1166C>G (p.Pro389Arg)
| |
14 | g.28768445C>T | CA389476679 | FOXG1 | c.1166C>T (p.Pro389Leu)
| |
14 | g.28768446C>A | CA486098372 | FOXG1 | c.1167C>A (p.Pro389=)
| |
14 | g.28768446C= | CA2126000419 | FOXG1 | c.1167C= (p.Pro389=)
| |
14 | g.28768446C>G | CA486098373 | FOXG1 | c.1167C>G (p.Pro389=)
| |
14 | g.28768446C>T | CA486098374 | FOXG1 | c.1167C>T (p.Pro389=)
| dbSNP gnomAD v3 gnomAD v4 |
14 | g.28768447T>A | CA389476681 | FOXG1 | c.1168T>A (p.Cys390Ser)
| |
14 | g.28768447T>C | CA389476682 | FOXG1 | c.1168T>C (p.Cys390Arg)
| |
14 | g.28768447T>G | CA389476680 | FOXG1 | c.1168T>G (p.Cys390Gly)
| |
14 | g.28768447dup | CA1139663432 | FOXG1 | c.1168dup (p.Cys390LeufsTer?)
| ClinVar dbSNP |
14 | g.28768448G>A | CA389476683 | FOXG1 | c.1169G>A (p.Cys390Tyr)
| |
14 | g.28768448G>C | CA389476684 | FOXG1 | c.1169G>C (p.Cys390Ser)
| |
14 | g.28768448G>T | CA389476685 | FOXG1 | c.1169G>T (p.Cys390Phe)
| |
14 | g.28768449C>A | CA389476686 | FOXG1 | c.1170C>A (p.Cys390Ter)
| ClinVar dbSNP |
14 | g.28768449C= | CA2126000420 | FOXG1 | c.1170C= (p.Cys390=)
| |
14 | g.28768449C>G | CA389476687 | FOXG1 | c.1170C>G (p.Cys390Trp)
| |
14 | g.28768449C>T | CA486098376 | FOXG1 | c.1170C>T (p.Cys390=)
| dbSNP gnomAD v2 gnomAD v3 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 |