14 | g.28768287C>A | CA389476334 | FOXG1 | c.1008C>A (p.Ser336Arg)
| COSMIC |
14 | g.28768287C= | CA2126000359 | FOXG1 | c.1008C= (p.Ser336=)
| |
14 | g.28768287C>G | CA389476335 | FOXG1 | c.1008C>G (p.Ser336Arg)
| gnomAD v4 |
14 | g.28768287C>T | CA486098416 | FOXG1 | c.1008C>T (p.Ser336=)
| dbSNP |
14 | g.28768290_28768294dup | CA1139663429 | FOXG1 | c.1011_1015dup (p.Met339ThrfsTer9)
| ClinVar dbSNP |
14 | g.28768288C>A | CA389476336 | FOXG1 | c.1009C>A (p.His337Asn)
| COSMIC |
14 | g.28768288C>G | CA389476337 | FOXG1 | c.1009C>G (p.His337Asp)
| |
14 | g.28768288C>T | CA389476338 | FOXG1 | c.1009C>T (p.His337Tyr)
| |
14 | g.28768289A= | CA2126000360 | FOXG1 | c.1010A= (p.His337=)
| |
14 | g.28768289A>C | CA389476339 | FOXG1 | c.1010A>C (p.His337Pro)
| |
14 | g.28768289A>G | CA389476340 | FOXG1 | c.1010A>G (p.His337Arg)
| |
14 | g.28768289A>T | CA389476341 | FOXG1 | c.1010A>T (p.His337Leu)
| |
14 | g.28768290C>A | CA389476342 | FOXG1 | c.1011C>A (p.His337Gln)
| |
14 | g.28768290C= | CA2126000361 | FOXG1 | c.1011C= (p.His337=)
| |
14 | g.28768290C>G | CA389476343 | FOXG1 | c.1011C>G (p.His337Gln)
| |
14 | g.28768290C>T | CA486098417 | FOXG1 | c.1011C>T (p.His337=)
| ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.28768293dup | CA916083365 | FOXG1 | c.1014dup (p.Met339HisfsTer?)
| ClinVar dbSNP |
14 | g.28768291C>A | CA389476344 | FOXG1 | c.1012C>A (p.Pro338Thr)
| gnomAD v4 |
14 | g.28768291C>G | CA389476345 | FOXG1 | c.1012C>G (p.Pro338Ala)
| |
14 | g.28768291C>T | CA389476346 | FOXG1 | c.1012C>T (p.Pro338Ser)
| COSMIC |
14 | g.28768292C>A | CA389476347 | FOXG1 | c.1013C>A (p.Pro338His)
| gnomAD v4 |
14 | g.28768292C>G | CA389476348 | FOXG1 | c.1013C>G (p.Pro338Arg)
| |
14 | g.28768292C>T | CA389476349 | FOXG1 | c.1013C>T (p.Pro338Leu)
| |
14 | g.28768293C>A | CA486098419 | FOXG1 | c.1014C>A (p.Pro338=)
| |
14 | g.28768293C>G | CA486098420 | FOXG1 | c.1014C>G (p.Pro338=)
| |
14 | g.28768293C>T | CA486098421 | FOXG1 | c.1014C>T (p.Pro338=)
| gnomAD v4 |
14 | g.28768294A>C | CA389476350 | FOXG1 | c.1015A>C (p.Met339Leu)
| |
14 | g.28768294A>G | CA389476351 | FOXG1 | c.1015A>G (p.Met339Val)
| |
14 | g.28768294A>T | CA389476352 | FOXG1 | c.1015A>T (p.Met339Leu)
| |
14 | g.28768295T>A | CA389476353 | FOXG1 | c.1016T>A (p.Met339Lys)
| |
14 | g.28768295T>C | CA389476354 | FOXG1 | c.1016T>C (p.Met339Thr)
| |
14 | g.28768295T>G | CA389476355 | FOXG1 | c.1016T>G (p.Met339Arg)
| |
14 | g.28768296G>A | CA389476358 | FOXG1 | c.1017G>A (p.Met339Ile)
| dbSNP gnomAD v2 gnomAD v4 |
14 | g.28768296G>C | CA389476357 | FOXG1 | c.1017G>C (p.Met339Ile)
| |
14 | g.28768296G= | CA2126000362 | FOXG1 | c.1017G= (p.Met339=)
| |
14 | g.28768296G>T | CA389476356 | FOXG1 | c.1017G>T (p.Met339Ile)
| gnomAD v4 |
14 | g.28768297C>A | CA389476359 | FOXG1 | c.1018C>A (p.Pro340Thr)
| |
14 | g.28768297C= | CA2126000363 | FOXG1 | c.1018C= (p.Pro340=)
| |
14 | g.28768297C>G | CA389476360 | FOXG1 | c.1018C>G (p.Pro340Ala)
| |
14 | g.28768297C>T | CA389476361 | FOXG1 | c.1018C>T (p.Pro340Ser)
| dbSNP gnomAD v2 gnomAD v4 |
14 | g.28768299del | CA2573149904 | FOXG1 | c.1020del (p.Tyr341ThrfsTer5)
| ClinVar dbSNP |
14 | g.28768298C>A | CA389476362 | FOXG1 | c.1019C>A (p.Pro340His)
| COSMIC |
14 | g.28768298C>G | CA389476363 | FOXG1 | c.1019C>G (p.Pro340Arg)
| gnomAD v4 |
14 | g.28768298C>T | CA389476364 | FOXG1 | c.1019C>T (p.Pro340Leu)
| |
14 | g.28768300_28768308del | CA2741363690 | FOXG1 | c.1021_1029del (p.Tyr341_Ser343del)
| |
14 | g.28768299C>A | CA486098428 | FOXG1 | c.1020C>A (p.Pro340=)
| |
14 | g.28768299C>G | CA486098429 | FOXG1 | c.1020C>G (p.Pro340=)
| |
14 | g.28768299C>T | CA486098430 | FOXG1 | c.1020C>T (p.Pro340=)
| ClinVar dbSNP |
14 | g.28768300T>A | CA389476365 | FOXG1 | c.1021T>A (p.Tyr341Asn)
| |
14 | g.28768300T>C | CA389476366 | FOXG1 | c.1021T>C (p.Tyr341His)
| |
14 | g.28768300T>G | CA389476367 | FOXG1 | c.1021T>G (p.Tyr341Asp)
| |
14 | g.28768300dup | CA658770580 | FOXG1 | c.1021dup (p.Tyr341LeufsTer?)
| |
14 | g.28768301A>C | CA389476368 | FOXG1 | c.1022A>C (p.Tyr341Ser)
| |
14 | g.28768301A>G | CA389476369 | FOXG1 | c.1022A>G (p.Tyr341Cys)
| |
14 | g.28768301A>T | CA389476370 | FOXG1 | c.1022A>T (p.Tyr341Phe)
| |
14 | g.28768302C>A | CA389476371 | FOXG1 | c.1023C>A (p.Tyr341Ter)
| |
14 | g.28768302C= | CA2126000364 | FOXG1 | c.1023C= (p.Tyr341=)
| |
14 | g.28768302C>G | CA389476372 | FOXG1 | c.1023C>G (p.Tyr341Ter)
| ClinVar dbSNP |
14 | g.28768302C>T | CA7140649 | FOXG1 | c.1023C>T (p.Tyr341=)
| dbSNP ExAC gnomAD v2 |
14 | g.28768303A= | CA2126000365 | FOXG1 | c.1024A= (p.Ser342=)
| |
14 | g.28768303A>C | CA389476373 | FOXG1 | c.1024A>C (p.Ser342Arg)
| |
14 | g.28768303A>G | CA389476375 | FOXG1 | c.1024A>G (p.Ser342Gly)
| dbSNP gnomAD v4 |
14 | g.28768303A>T | CA389476374 | FOXG1 | c.1024A>T (p.Ser342Cys)
| |
14 | g.28768304G>A | CA389476376 | FOXG1 | c.1025G>A (p.Ser342Asn)
| |
14 | g.28768304G>C | CA389476378 | FOXG1 | c.1025G>C (p.Ser342Thr)
| |
14 | g.28768304G>T | CA389476377 | FOXG1 | c.1025G>T (p.Ser342Ile)
| |
14 | g.28768305C>A | CA389476379 | FOXG1 | c.1026C>A (p.Ser342Arg)
| |
14 | g.28768305C= | CA2126000366 | FOXG1 | c.1026C= (p.Ser342=)
| |
14 | g.28768305C>G | CA389476380 | FOXG1 | c.1026C>G (p.Ser342Arg)
| |
14 | g.28768305C>T | CA7140650 | FOXG1 | c.1026C>T (p.Ser342=)
| dbSNP ExAC gnomAD v2 |
14 | g.28768306T>A | CA389476381 | FOXG1 | c.1027T>A (p.Ser343Thr)
| |
14 | g.28768306T>C | CA389476382 | FOXG1 | c.1027T>C (p.Ser343Pro)
| |
14 | g.28768306T>G | CA389476383 | FOXG1 | c.1027T>G (p.Ser343Ala)
| |
14 | g.28768307C>A | CA389476384 | FOXG1 | c.1028C>A (p.Ser343Tyr)
| |
14 | g.28768307C= | CA2126000367 | FOXG1 | c.1028C= (p.Ser343=)
| |
14 | g.28768307C>G | CA389476385 | FOXG1 | c.1028C>G (p.Ser343Cys)
| |
14 | g.28768307C>T | CA389476386 | FOXG1 | c.1028C>T (p.Ser343Phe)
| dbSNP gnomAD v2 |
14 | g.28768308C>A | CA486098441 | FOXG1 | c.1029C>A (p.Ser343=)
| |
14 | g.28768308C>G | CA486098445 | FOXG1 | c.1029C>G (p.Ser343=)
| |
14 | g.28768308C>T | CA486098443 | FOXG1 | c.1029C>T (p.Ser343=)
| ClinVar |
14 | g.28768309G>A | CA7140651 | FOXG1 | c.1030G>A (p.Val344Met)
| dbSNP ExAC gnomAD v2 |
14 | g.28768309G>C | CA389476388 | FOXG1 | c.1030G>C (p.Val344Leu)
| |
14 | g.28768309G= | CA2126000368 | FOXG1 | c.1030G= (p.Val344=)
| |
14 | g.28768309G>T | CA389476387 | FOXG1 | c.1030G>T (p.Val344Leu)
| |
14 | g.28768311_28768312del | CA2695199810 | FOXG1 | c.1032_1033del (p.Leu345AspfsTer?)
| ClinVar |
14 | g.28768310T>A | CA389476389 | FOXG1 | c.1031T>A (p.Val344Glu)
| |
14 | g.28768310T>C | CA389476390 | FOXG1 | c.1031T>C (p.Val344Ala)
| |
14 | g.28768310T>G | CA389476391 | FOXG1 | c.1031T>G (p.Val344Gly)
| |
14 | g.28768311G>A | CA486098451 | FOXG1 | c.1032G>A (p.Val344=)
| |
14 | g.28768311G>C | CA486098453 | FOXG1 | c.1032G>C (p.Val344=)
| ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.28768311G= | CA2126000369 | FOXG1 | c.1032G= (p.Val344=)
| |
14 | g.28768311G>T | CA7140652 | FOXG1 | c.1032G>T (p.Val344=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
14 | g.28768312T>A | CA389476392 | FOXG1 | c.1033T>A (p.Leu345Met)
| |
14 | g.28768312T>C | CA486098454 | FOXG1 | c.1033T>C (p.Leu345=)
| |
14 | g.28768312T>G | CA389476393 | FOXG1 | c.1033T>G (p.Leu345Val)
| |
14 | g.28768313T>A | CA389476394 | FOXG1 | c.1034T>A (p.Leu345Ter)
| |
14 | g.28768313T>C | CA389476395 | FOXG1 | c.1034T>C (p.Leu345Ser)
| |
14 | g.28768313T>G | CA389476396 | FOXG1 | c.1034T>G (p.Leu345Trp)
| |
14 | g.28768314G>A | CA486098456 | FOXG1 | c.1035G>A (p.Leu345=)
| |
14 | g.28768314G>C | CA389476397 | FOXG1 | c.1035G>C (p.Leu345Phe)
| |
14 | g.28768314G>T | CA389476398 | FOXG1 | c.1035G>T (p.Leu345Phe)
| |
14 | g.28768315A>C | CA389476400 | FOXG1 | c.1036A>C (p.Thr346Pro)
| gnomAD v4 |
14 | g.28768315A>G | CA389476401 | FOXG1 | c.1036A>G (p.Thr346Ala)
| |
14 | g.28768315A>T | CA389476399 | FOXG1 | c.1036A>T (p.Thr346Ser)
| |
14 | g.28768316del | CA2739277847 | FOXG1 | c.1037del (p.Thr346IlefsTer17)
| ClinVar |
14 | g.28768316C>A | CA389476402 | FOXG1 | c.1037C>A (p.Thr346Asn)
| |
14 | g.28768316C>G | CA389476403 | FOXG1 | c.1037C>G (p.Thr346Ser)
| |
14 | g.28768316C>T | CA389476404 | FOXG1 | c.1037C>T (p.Thr346Ile)
| COSMIC |
14 | g.28768317T>A | CA486098462 | FOXG1 | c.1038T>A (p.Thr346=)
| |
14 | g.28768317T>C | CA486098465 | FOXG1 | c.1038T>C (p.Thr346=)
| |
14 | g.28768317T>G | CA486098467 | FOXG1 | c.1038T>G (p.Thr346=)
| |
14 | g.28768318C>A | CA389476405 | FOXG1 | c.1039C>A (p.Gln347Lys)
| |
14 | g.28768318C>G | CA389476406 | FOXG1 | c.1039C>G (p.Gln347Glu)
| |
14 | g.28768318C>T | CA389476407 | FOXG1 | c.1039C>T (p.Gln347Ter)
| |
14 | g.28768319A>C | CA389476408 | FOXG1 | c.1040A>C (p.Gln347Pro)
| ClinVar gnomAD v4 |
14 | g.28768319A>G | CA389476409 | FOXG1 | c.1040A>G (p.Gln347Arg)
| |
14 | g.28768319A>T | CA389476410 | FOXG1 | c.1040A>T (p.Gln347Leu)
| |
14 | g.28768320G>A | CA486098470 | FOXG1 | c.1041G>A (p.Gln347=)
| gnomAD v4 COSMIC |
14 | g.28768320G>C | CA389476411 | FOXG1 | c.1041G>C (p.Gln347His)
| |
14 | g.28768320G>T | CA389476412 | FOXG1 | c.1041G>T (p.Gln347His)
| |
14 | g.28768321A>C | CA389476415 | FOXG1 | c.1042A>C (p.Asn348His)
| |
14 | g.28768321A>G | CA389476414 | FOXG1 | c.1042A>G (p.Asn348Asp)
| |
14 | g.28768321A>T | CA389476413 | FOXG1 | c.1042A>T (p.Asn348Tyr)
| |
14 | g.28768322A>C | CA389476416 | FOXG1 | c.1043A>C (p.Asn348Thr)
| |
14 | g.28768322A>G | CA389476417 | FOXG1 | c.1043A>G (p.Asn348Ser)
| ClinVar |
14 | g.28768322A>T | CA389476418 | FOXG1 | c.1043A>T (p.Asn348Ile)
| |
14 | g.28768323C>A | CA389476419 | FOXG1 | c.1044C>A (p.Asn348Lys)
| |
14 | g.28768323C= | CA2126000370 | FOXG1 | c.1044C= (p.Asn348=)
| |
14 | g.28768323C>G | CA389476420 | FOXG1 | c.1044C>G (p.Asn348Lys)
| |
14 | g.28768323C>T | CA486098477 | FOXG1 | c.1044C>T (p.Asn348=)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.28768324T>A | CA389476421 | FOXG1 | c.1045T>A (p.Ser349Thr)
| |
14 | g.28768324T>C | CA389476422 | FOXG1 | c.1045T>C (p.Ser349Pro)
| |
14 | g.28768324T>G | CA314631 | FOXG1 | c.1045T>G (p.Ser349Ala)
| ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.28768324T= | CA2126000371 | FOXG1 | c.1045T= (p.Ser349=)
| |
14 | g.28768325C>A | CA389476423 | FOXG1 | c.1046C>A (p.Ser349Ter)
| |
14 | g.28768325C>G | CA389476424 | FOXG1 | c.1046C>G (p.Ser349Trp)
| |
14 | g.28768325C>T | CA389476425 | FOXG1 | c.1046C>T (p.Ser349Leu)
| COSMIC |
14 | g.28768326G>A | CA486098480 | FOXG1 | c.1047G>A (p.Ser349=)
| |
14 | g.28768326G>C | CA486098482 | FOXG1 | c.1047G>C (p.Ser349=)
| |
14 | g.28768326G= | CA2126000372 | FOXG1 | c.1047G= (p.Ser349=)
| |
14 | g.28768326G>T | CA486098484 | FOXG1 | c.1047G>T (p.Ser349=)
| dbSNP gnomAD v4 |
14 | g.28768327C>A | CA389476426 | FOXG1 | c.1048C>A (p.Leu350Met)
| |
14 | g.28768327C= | CA2126000373 | FOXG1 | c.1048C= (p.Leu350=)
| |
14 | g.28768327C>G | CA389476427 | FOXG1 | c.1048C>G (p.Leu350Val)
| gnomAD v4 |
14 | g.28768327C>T | CA486098485 | FOXG1 | c.1048C>T (p.Leu350=)
| dbSNP gnomAD v2 gnomAD v4 COSMIC |
14 | g.28768328T>A | CA389476429 | FOXG1 | c.1049T>A (p.Leu350Gln)
| |
14 | g.28768328T>C | CA389476430 | FOXG1 | c.1049T>C (p.Leu350Pro)
| |
14 | g.28768328T>G | CA389476428 | FOXG1 | c.1049T>G (p.Leu350Arg)
| |
14 | g.28768329G>A | CA486098486 | FOXG1 | c.1050G>A (p.Leu350=)
| COSMIC |
14 | g.28768329G>C | CA486098488 | FOXG1 | c.1050G>C (p.Leu350=)
| |
14 | g.28768329G>T | CA486098489 | FOXG1 | c.1050G>T (p.Leu350=)
| |
14 | g.28768331del | CA2840770148 | FOXG1 | c.1052del (p.Gly351AlafsTer12)
| |
14 | g.28768330G>A | CA389476433 | FOXG1 | c.1051G>A (p.Gly351Ser)
| gnomAD v4 |
14 | g.28768330G>C | CA389476431 | FOXG1 | c.1051G>C (p.Gly351Arg)
| |
14 | g.28768330G>T | CA389476432 | FOXG1 | c.1051G>T (p.Gly351Cys)
| |
14 | g.28768331G>A | CA389476434 | FOXG1 | c.1052G>A (p.Gly351Asp)
| |
14 | g.28768331G>C | CA389476435 | FOXG1 | c.1052G>C (p.Gly351Ala)
| |
14 | g.28768331G>T | CA389476436 | FOXG1 | c.1052G>T (p.Gly351Val)
| |
14 | g.28768332C>A | CA486098492 | FOXG1 | c.1053C>A (p.Gly351=)
| |
14 | g.28768332C>G | CA486098494 | FOXG1 | c.1053C>G (p.Gly351=)
| gnomAD v4 |
14 | g.28768332C>T | CA486098495 | FOXG1 | c.1053C>T (p.Gly351=)
| gnomAD v4 |
14 | g.28768333A>C | CA389476437 | FOXG1 | c.1054A>C (p.Asn352His)
| |
14 | g.28768333A>G | CA389476438 | FOXG1 | c.1054A>G (p.Asn352Asp)
| |
14 | g.28768333A>T | CA389476439 | FOXG1 | c.1054A>T (p.Asn352Tyr)
| |
14 | g.28768334A= | CA2126000374 | FOXG1 | c.1055A= (p.Asn352=)
| |
14 | g.28768334A>C | CA389476440 | FOXG1 | c.1055A>C (p.Asn352Thr)
| dbSNP gnomAD v2 gnomAD v4 |
14 | g.28768334A>G | CA389476441 | FOXG1 | c.1055A>G (p.Asn352Ser)
| |
14 | g.28768334A>T | CA389476442 | FOXG1 | c.1055A>T (p.Asn352Ile)
| |
14 | g.28768335C>A | CA389476443 | FOXG1 | c.1056C>A (p.Asn352Lys)
| |
14 | g.28768335C= | CA2126000375 | FOXG1 | c.1056C= (p.Asn352=)
| |
14 | g.28768335C>G | CA389476444 | FOXG1 | c.1056C>G (p.Asn352Lys)
| |
14 | g.28768335C>T | CA486098498 | FOXG1 | c.1056C>T (p.Asn352=)
| |
14 | g.28768336A>C | CA389476445 | FOXG1 | c.1057A>C (p.Asn353His)
| |
14 | g.28768336A>G | CA389476447 | FOXG1 | c.1057A>G (p.Asn353Asp)
| |
14 | g.28768336A>T | CA389476446 | FOXG1 | c.1057A>T (p.Asn353Tyr)
| |
14 | g.28768337dup | CA16619865 | FOXG1 | c.1058dup (p.Asn353LysfsTer?)
| ClinVar dbSNP |
14 | g.28768337A= | CA2126000376 | FOXG1 | c.1058A= (p.Asn353=)
| |
14 | g.28768337A>C | CA389476448 | FOXG1 | c.1058A>C (p.Asn353Thr)
| |
14 | g.28768337A>G | CA7140653 | FOXG1 | c.1058A>G (p.Asn353Ser)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
14 | g.28768337A>T | CA389476449 | FOXG1 | c.1058A>T (p.Asn353Ile)
| |
14 | g.28768338C>A | CA389476450 | FOXG1 | c.1059C>A (p.Asn353Lys)
| |
14 | g.28768338C>G | CA389476451 | FOXG1 | c.1059C>G (p.Asn353Lys)
| |
14 | g.28768338C>T | CA486098504 | FOXG1 | c.1059C>T (p.Asn353=)
| |
14 | g.28768339del | CA2830782522 | FOXG1 | c.1060del (p.His354ThrfsTer9)
| |
14 | g.28768339C>A | CA389476452 | FOXG1 | c.1060C>A (p.His354Asn)
| |
14 | g.28768339C>G | CA389476453 | FOXG1 | c.1060C>G (p.His354Asp)
| |
14 | g.28768339C>T | CA389476454 | FOXG1 | c.1060C>T (p.His354Tyr)
| |
14 | g.28768340A>C | CA389476455 | FOXG1 | c.1061A>C (p.His354Pro)
| gnomAD v4 |
14 | g.28768340A>G | CA389476456 | FOXG1 | c.1061A>G (p.His354Arg)
| |
14 | g.28768340A>T | CA389476457 | FOXG1 | c.1061A>T (p.His354Leu)
| |
14 | g.28768340_28768341delinsAC | CA2126000377 | FOXG1 | c.1061_1062delinsAC (p.His354=)
| |
14 | g.28768341del | CA1139663430 | FOXG1 | c.1062del (p.Ser355ProfsTer8)
| ClinVar dbSNP |
14 | g.28768341C>A | CA389476459 | FOXG1 | c.1062C>A (p.His354Gln)
| |
14 | g.28768341C= | CA2126000378 | FOXG1 | c.1062C= (p.His354=)
| |
14 | g.28768341C>G | CA389476458 | FOXG1 | c.1062C>G (p.His354Gln)
| |
14 | g.28768341C>T | CA258396592 | FOXG1 | c.1062C>T (p.His354=)
| ClinVar dbSNP gnomAD v3 gnomAD v4 |
14 | g.28768342T>A | CA389476460 | FOXG1 | c.1063T>A (p.Ser355Thr)
| |
14 | g.28768342T>C | CA389476462 | FOXG1 | c.1063T>C (p.Ser355Pro)
| |
14 | g.28768342T>G | CA389476461 | FOXG1 | c.1063T>G (p.Ser355Ala)
| |
14 | g.28768343C>A | CA389476463 | FOXG1 | c.1064C>A (p.Ser355Tyr)
| |
14 | g.28768343C>G | CA389476464 | FOXG1 | c.1064C>G (p.Ser355Cys)
| |
14 | g.28768343C>T | CA389476465 | FOXG1 | c.1064C>T (p.Ser355Phe)
| |
14 | g.28768343_28768346delinsCCTT | CA2126000379 | FOXG1 | c.1064_1067delinsCCTT (p.Ser355=)
| |
14 | g.28768344C>A | CA486098510 | FOXG1 | c.1065C>A (p.Ser355=)
| |
14 | g.28768344C= | CA2126000382 | FOXG1 | c.1065C= (p.Ser355=)
| |
14 | g.28768344C>G | CA486098511 | FOXG1 | c.1065C>G (p.Ser355=)
| ClinVar dbSNP gnomAD v4 |
14 | g.28768344C>T | CA486098512 | FOXG1 | c.1065C>T (p.Ser355=)
| ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC |
14 | g.28768344_28768345delinsCT | CA2126000381 | FOXG1 | c.1065_1066delinsCT (p.Ser355=)
| |
14 | g.28768346_28768348del | CA2126000380 | FOXG1 | c.1067_1069del (p.Phe356del)
| dbSNP gnomAD v4 |
14 | g.28768345T>A | CA389476466 | FOXG1 | c.1066T>A (p.Phe356Ile)
| |
14 | g.28768345T>C | CA389476467 | FOXG1 | c.1066T>C (p.Phe356Leu)
| |
14 | g.28768345T>G | CA389476468 | FOXG1 | c.1066T>G (p.Phe356Val)
| |
14 | g.28768346del | CA658798200 | FOXG1 | c.1067del (p.Phe356SerfsTer7)
| ClinVar dbSNP |
14 | g.28768346T>A | CA389476469 | FOXG1 | c.1067T>A (p.Phe356Tyr)
| |
14 | g.28768346T>C | CA389476470 | FOXG1 | c.1067T>C (p.Phe356Ser)
| |
14 | g.28768346T>G | CA389476471 | FOXG1 | c.1067T>G (p.Phe356Cys)
| |
14 | g.28768347C>A | CA389476472 | FOXG1 | c.1068C>A (p.Phe356Leu)
| |
14 | g.28768347C>G | CA389476473 | FOXG1 | c.1068C>G (p.Phe356Leu)
| |
14 | g.28768347C>T | CA486098518 | FOXG1 | c.1068C>T (p.Phe356=)
| |
14 | g.28768348_28768350del | CA2624400221 | FOXG1 | c.1069_1071del (p.Ser357del)
| gnomAD v4 |
14 | g.28768348T>A | CA389476476 | FOXG1 | c.1069T>A (p.Ser357Thr)
| |
14 | g.28768348T>C | CA389476475 | FOXG1 | c.1069T>C (p.Ser357Pro)
| |
14 | g.28768348T>G | CA389476474 | FOXG1 | c.1069T>G (p.Ser357Ala)
| |
14 | g.28768349C>A | CA389476477 | FOXG1 | c.1070C>A (p.Ser357Tyr)
| |
14 | g.28768349C>G | CA389476478 | FOXG1 | c.1070C>G (p.Ser357Cys)
| |
14 | g.28768349C>T | CA389476479 | FOXG1 | c.1070C>T (p.Ser357Phe)
| |
14 | g.28768350del | CA2840770149 | FOXG1 | c.1071del (p.Thr358ProfsTer5)
| |
14 | g.28768351_28768353del | CA2624400222 | FOXG1 | c.1072_1074del (p.Thr358del)
| gnomAD v4 |
14 | g.28768350C>A | CA486098524 | FOXG1 | c.1071C>A (p.Ser357=)
| COSMIC |
14 | g.28768350C= | CA2126000383 | FOXG1 | c.1071C= (p.Ser357=)
| |
14 | g.28768350C>G | CA486098525 | FOXG1 | c.1071C>G (p.Ser357=)
| |
14 | g.28768350C>T | CA7140654 | FOXG1 | c.1071C>T (p.Ser357=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.28768351A>C | CA389476480 | FOXG1 | c.1072A>C (p.Thr358Pro)
| |
14 | g.28768351A>G | CA389476481 | FOXG1 | c.1072A>G (p.Thr358Ala)
| |
14 | g.28768351A>T | CA389476482 | FOXG1 | c.1072A>T (p.Thr358Ser)
| |
14 | g.28768352C>A | CA389476483 | FOXG1 | c.1073C>A (p.Thr358Asn)
| |
14 | g.28768352C>G | CA389476484 | FOXG1 | c.1073C>G (p.Thr358Ser)
| |
14 | g.28768352C>T | CA389476485 | FOXG1 | c.1073C>T (p.Thr358Ile)
| |
14 | g.28768353dup | CA2840770150 | FOXG1 | c.1074dup (p.Ala359ArgfsTer?)
| |
14 | g.28768353del | CA2697553886 | FOXG1 | c.1074del (p.Ala359ProfsTer4)
| ClinVar |
14 | g.28768353C>A | CA486098531 | FOXG1 | c.1074C>A (p.Thr358=)
| gnomAD v4 |
14 | g.28768353C>G | CA486098532 | FOXG1 | c.1074C>G (p.Thr358=)
| gnomAD v4 |
14 | g.28768353C>T | CA486098533 | FOXG1 | c.1074C>T (p.Thr358=)
| COSMIC |
14 | g.28768354G>A | CA389476486 | FOXG1 | c.1075G>A (p.Ala359Thr)
| |
14 | g.28768354G>C | CA389476487 | FOXG1 | c.1075G>C (p.Ala359Pro)
| COSMIC |
14 | g.28768354G>T | CA389476488 | FOXG1 | c.1075G>T (p.Ala359Ser)
| |
14 | g.28768355C>A | CA389476491 | FOXG1 | c.1076C>A (p.Ala359Asp)
| |
14 | g.28768355C>G | CA389476490 | FOXG1 | c.1076C>G (p.Ala359Gly)
| |
14 | g.28768355C>T | CA389476489 | FOXG1 | c.1076C>T (p.Ala359Val)
| |
14 | g.28768356C>A | CA486098542 | FOXG1 | c.1077C>A (p.Ala359=)
| dbSNP gnomAD v3 gnomAD v4 |
14 | g.28768356C= | CA2126000384 | FOXG1 | c.1077C= (p.Ala359=)
| |
14 | g.28768356C>G | CA486098544 | FOXG1 | c.1077C>G (p.Ala359=)
| |
14 | g.28768356C>T | CA486098545 | FOXG1 | c.1077C>T (p.Ala359=)
| dbSNP gnomAD v2 gnomAD v4 |
14 | g.28768357A>C | CA389476493 | FOXG1 | c.1078A>C (p.Asn360His)
| |
14 | g.28768357A>G | CA389476492 | FOXG1 | c.1078A>G (p.Asn360Asp)
| |
14 | g.28768357A>T | CA389476494 | FOXG1 | c.1078A>T (p.Asn360Tyr)
| |
14 | g.28768358A>C | CA389476495 | FOXG1 | c.1079A>C (p.Asn360Thr)
| |
14 | g.28768358A>G | CA389476497 | FOXG1 | c.1079A>G (p.Asn360Ser)
| |
14 | g.28768358A>T | CA389476496 | FOXG1 | c.1079A>T (p.Asn360Ile)
| |
14 | g.28768359C>A | CA389476498 | FOXG1 | c.1080C>A (p.Asn360Lys)
| gnomAD v4 COSMIC |
14 | g.28768359C= | CA2126000385 | FOXG1 | c.1080C= (p.Asn360=)
| |
14 | g.28768359C>G | CA389476499 | FOXG1 | c.1080C>G (p.Asn360Lys)
| |
14 | g.28768359C>T | CA486098547 | FOXG1 | c.1080C>T (p.Asn360=)
| gnomAD v4 COSMIC |
14 | g.28768360G>A | CA389476500 | FOXG1 | c.1081G>A (p.Gly361Ser)
| ClinVar dbSNP COSMIC |
14 | g.28768360G>C | CA389476501 | FOXG1 | c.1081G>C (p.Gly361Arg)
| |
14 | g.28768360G= | CA2126000386 | FOXG1 | c.1081G= (p.Gly361=)
| |
14 | g.28768360G>T | CA389476502 | FOXG1 | c.1081G>T (p.Gly361Cys)
| |
14 | g.28768361dup | CA658770581 | FOXG1 | c.1082dup (p.Leu362ProfsTer?)
| ClinVar dbSNP |
14 | g.28768361G>A | CA389476503 | FOXG1 | c.1082G>A (p.Gly361Asp)
| |
14 | g.28768361G>C | CA389476504 | FOXG1 | c.1082G>C (p.Gly361Ala)
| |
14 | g.28768361G>T | CA389476505 | FOXG1 | c.1082G>T (p.Gly361Val)
| |
14 | g.28768362C>A | CA486098557 | FOXG1 | c.1083C>A (p.Gly361=)
| |
14 | g.28768362C>G | CA486098556 | FOXG1 | c.1083C>G (p.Gly361=)
| COSMIC |
14 | g.28768362C>T | CA486098555 | FOXG1 | c.1083C>T (p.Gly361=)
| gnomAD v4 |
14 | g.28768363C>A | CA389476506 | FOXG1 | c.1084C>A (p.Leu362Met)
| |
14 | g.28768363C= | CA2126000387 | FOXG1 | c.1084C= (p.Leu362=)
| |
14 | g.28768363C>G | CA389476507 | FOXG1 | c.1084C>G (p.Leu362Val)
| |
14 | g.28768363C>T | CA486098558 | FOXG1 | c.1084C>T (p.Leu362=)
| ClinVar dbSNP |
14 | g.28768364T>A | CA389476508 | FOXG1 | c.1085T>A (p.Leu362Gln)
| |
14 | g.28768364T>C | CA389476509 | FOXG1 | c.1085T>C (p.Leu362Pro)
| |
14 | g.28768364T>G | CA389476510 | FOXG1 | c.1085T>G (p.Leu362Arg)
| |
14 | g.28768365G>A | CA172173 | FOXG1 | c.1086G>A (p.Leu362=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.28768365G>C | CA486098570 | FOXG1 | c.1086G>C (p.Leu362=)
| gnomAD v4 |
14 | g.28768365G= | CA2126000388 | FOXG1 | c.1086G= (p.Leu362=)
| |
14 | g.28768365G>T | CA486098566 | FOXG1 | c.1086G>T (p.Leu362=)
| |
14 | g.28768366A>C | CA389476511 | FOXG1 | c.1087A>C (p.Ser363Arg)
| |
14 | g.28768366A>G | CA389476512 | FOXG1 | c.1087A>G (p.Ser363Gly)
| |
14 | g.28768366A>T | CA389476513 | FOXG1 | c.1087A>T (p.Ser363Cys)
| |
14 | g.28768367G>A | CA389476514 | FOXG1 | c.1088G>A (p.Ser363Asn)
| |
14 | g.28768367G>C | CA389476515 | FOXG1 | c.1088G>C (p.Ser363Thr)
| gnomAD v4 |
14 | g.28768367G>T | CA389476516 | FOXG1 | c.1088G>T (p.Ser363Ile)
| |
14 | g.28768368C>A | CA389476517 | FOXG1 | c.1089C>A (p.Ser363Arg)
| |
14 | g.28768368C= | CA2126000389 | FOXG1 | c.1089C= (p.Ser363=)
| |
14 | g.28768368C>G | CA389476518 | FOXG1 | c.1089C>G (p.Ser363Arg)
| |
14 | g.28768368C>T | CA486098574 | FOXG1 | c.1089C>T (p.Ser363=)
| dbSNP gnomAD v2 COSMIC |
14 | g.28768369G>A | CA389476519 | FOXG1 | c.1090G>A (p.Val364Met)
| |
14 | g.28768369G>C | CA389476520 | FOXG1 | c.1090G>C (p.Val364Leu)
| |
14 | g.28768369G>T | CA389476521 | FOXG1 | c.1090G>T (p.Val364Leu)
| |
14 | g.28768370T>A | CA389476522 | FOXG1 | c.1091T>A (p.Val364Glu)
| |
14 | g.28768370T>C | CA389476523 | FOXG1 | c.1091T>C (p.Val364Ala)
| |
14 | g.28768370T>G | CA389476524 | FOXG1 | c.1091T>G (p.Val364Gly)
| |
14 | g.28768371G>A | CA486098577 | FOXG1 | c.1092G>A (p.Val364=)
| |
14 | g.28768371G>C | CA258396593 | FOXG1 | c.1092G>C (p.Val364=)
| ClinVar dbSNP gnomAD v4 |
14 | g.28768371G= | CA2126000390 | FOXG1 | c.1092G= (p.Val364=)
| |
14 | g.28768371G>T | CA486098580 | FOXG1 | c.1092G>T (p.Val364=)
| dbSNP gnomAD v3 gnomAD v4 |
14 | g.28768372G>A | CA389476527 | FOXG1 | c.1093G>A (p.Asp365Asn)
| |
14 | g.28768372G>C | CA389476525 | FOXG1 | c.1093G>C (p.Asp365His)
| |
14 | g.28768372G>T | CA389476526 | FOXG1 | c.1093G>T (p.Asp365Tyr)
| |
14 | g.28768374_28768393del | CA2573053900 | FOXG1 | c.1095_1114del (p.Arg366ProfsTer?)
| ClinVar dbSNP |
14 | g.28768373A>C | CA389476528 | FOXG1 | c.1094A>C (p.Asp365Ala)
| |
14 | g.28768373A>G | CA389476529 | FOXG1 | c.1094A>G (p.Asp365Gly)
| |
14 | g.28768373A>T | CA389476530 | FOXG1 | c.1094A>T (p.Asp365Val)
| |
14 | g.28768374C>A | CA389476531 | FOXG1 | c.1095C>A (p.Asp365Glu)
| |
14 | g.28768374C>G | CA389476532 | FOXG1 | c.1095C>G (p.Asp365Glu)
| |
14 | g.28768374C>T | CA486098583 | FOXG1 | c.1095C>T (p.Asp365=)
| gnomAD v4 |
14 | g.28768375C>A | CA486098586 | FOXG1 | c.1096C>A (p.Arg366=)
| |
14 | g.28768375C>G | CA389476533 | FOXG1 | c.1096C>G (p.Arg366Gly)
| |
14 | g.28768375C>T | CA389476534 | FOXG1 | c.1096C>T (p.Arg366Trp)
| |
14 | g.28768376G>A | CA389476535 | FOXG1 | c.1097G>A (p.Arg366Gln)
| dbSNP |
14 | g.28768376G>C | CA389476536 | FOXG1 | c.1097G>C (p.Arg366Pro)
| |
14 | g.28768376G= | CA2126000391 | FOXG1 | c.1097G= (p.Arg366=)
| |
14 | g.28768376G>T | CA389476537 | FOXG1 | c.1097G>T (p.Arg366Leu)
| |
14 | g.28768377G>A | CA486098587 | FOXG1 | c.1098G>A (p.Arg366=)
| |
14 | g.28768377G>C | CA486098588 | FOXG1 | c.1098G>C (p.Arg366=)
| |
14 | g.28768377G= | CA2126000392 | FOXG1 | c.1098G= (p.Arg366=)
| |
14 | g.28768377G>T | CA7140655 | FOXG1 | c.1098G>T (p.Arg366=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.28768378C>A | CA389476538 | FOXG1 | c.1099C>A (p.Leu367Met)
| |
14 | g.28768378C= | CA2126000393 | FOXG1 | c.1099C= (p.Leu367=)
| |
14 | g.28768378C>G | CA389476539 | FOXG1 | c.1099C>G (p.Leu367Val)
| |
14 | g.28768378C>T | CA486098589 | FOXG1 | c.1099C>T (p.Leu367=)
| dbSNP gnomAD v2 |
14 | g.28768379T>A | CA389476542 | FOXG1 | c.1100T>A (p.Leu367Gln)
| |
14 | g.28768379T>C | CA389476541 | FOXG1 | c.1100T>C (p.Leu367Pro)
| |
14 | g.28768379T>G | CA389476540 | FOXG1 | c.1100T>G (p.Leu367Arg)
| |
14 | g.28768380G>A | CA486098591 | FOXG1 | c.1101G>A (p.Leu367=)
| COSMIC |
14 | g.28768380G>C | CA486098594 | FOXG1 | c.1101G>C (p.Leu367=)
| |
14 | g.28768380G>T | CA486098590 | FOXG1 | c.1101G>T (p.Leu367=)
| |
14 | g.28768381G>A | CA389476543 | FOXG1 | c.1102G>A (p.Val368Ile)
| |
14 | g.28768381G>C | CA389476544 | FOXG1 | c.1102G>C (p.Val368Leu)
| |
14 | g.28768381G>T | CA389476545 | FOXG1 | c.1102G>T (p.Val368Phe)
| |
14 | g.28768382T>A | CA389476546 | FOXG1 | c.1103T>A (p.Val368Asp)
| |
14 | g.28768382T>C | CA389476547 | FOXG1 | c.1103T>C (p.Val368Ala)
| |
14 | g.28768382T>G | CA7140656 | FOXG1 | c.1103T>G (p.Val368Gly)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.28768382T= | CA2126000394 | FOXG1 | c.1103T= (p.Val368=)
| |
14 | g.28768383C>A | CA7140657 | FOXG1 | c.1104C>A (p.Val368=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
14 | g.28768383C= | CA2126000395 | FOXG1 | c.1104C= (p.Val368=)
| |
14 | g.28768383C>G | CA486098598 | FOXG1 | c.1104C>G (p.Val368=)
| |
14 | g.28768383C>T | CA486098599 | FOXG1 | c.1104C>T (p.Val368=)
| |
14 | g.28768384A>C | CA389476548 | FOXG1 | c.1105A>C (p.Asn369His)
| |
14 | g.28768384A>G | CA389476549 | FOXG1 | c.1105A>G (p.Asn369Asp)
| |
14 | g.28768384A>T | CA389476550 | FOXG1 | c.1105A>T (p.Asn369Tyr)
| |
14 | g.28768385A>C | CA389476551 | FOXG1 | c.1106A>C (p.Asn369Thr)
| |
14 | g.28768385A>G | CA389476552 | FOXG1 | c.1106A>G (p.Asn369Ser)
| |
14 | g.28768385A>T | CA389476553 | FOXG1 | c.1106A>T (p.Asn369Ile)
| |
14 | g.28768386C>A | CA389476554 | FOXG1 | c.1107C>A (p.Asn369Lys)
| |
14 | g.28768386C= | CA2126000396 | FOXG1 | c.1107C= (p.Asn369=)
| |
14 | g.28768386C>G | CA389476555 | FOXG1 | c.1107C>G (p.Asn369Lys)
| |
14 | g.28768386C>T | CA7140658 | FOXG1 | c.1107C>T (p.Asn369=)
| dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
14 | g.28768387G>A | CA389476556 | FOXG1 | c.1108G>A (p.Gly370Arg)
| COSMIC |
14 | g.28768387G>C | CA389476558 | FOXG1 | c.1108G>C (p.Gly370Arg)
| |
14 | g.28768387G>T | CA389476557 | FOXG1 | c.1108G>T (p.Gly370Trp)
| |
14 | g.28768390dup | CA2832528762 | FOXG1 | c.1111dup (p.Glu371GlyfsTer?)
| |