| 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.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.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.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.28768388G>A | CA389476559 | FOXG1 | c.1109G>A (p.Gly370Glu)
| ClinVar dbSNP |
| 14 | g.28768388G>C | CA389476560 | FOXG1 | c.1109G>C (p.Gly370Ala)
| |
| 14 | g.28768388G>T | CA389476561 | FOXG1 | c.1109G>T (p.Gly370Val)
| |
| 14 | g.28768389G>A | CA486098615 | FOXG1 | c.1110G>A (p.Gly370=)
| |
| 14 | g.28768389G>C | CA486098621 | FOXG1 | c.1110G>C (p.Gly370=)
| |
| 14 | g.28768389G= | CA2126000397 | FOXG1 | c.1110G= (p.Gly370=)
| |
| 14 | g.28768389G>T | CA486098624 | FOXG1 | c.1110G>T (p.Gly370=)
| dbSNP |
| 14 | g.28768390G>A | CA389476562 | FOXG1 | c.1111G>A (p.Glu371Lys)
| |
| 14 | g.28768390G>C | CA389476563 | FOXG1 | c.1111G>C (p.Glu371Gln)
| |
| 14 | g.28768390G>T | CA389476564 | FOXG1 | c.1111G>T (p.Glu371Ter)
| ClinVar dbSNP |
| 14 | g.28768391A>C | CA389476565 | FOXG1 | c.1112A>C (p.Glu371Ala)
| |
| 14 | g.28768391A>G | CA389476566 | FOXG1 | c.1112A>G (p.Glu371Gly)
| |
| 14 | g.28768391A>T | CA389476567 | FOXG1 | c.1112A>T (p.Glu371Val)
| |
| 14 | g.28768392G>A | CA486098631 | FOXG1 | c.1113G>A (p.Glu371=)
| |
| 14 | g.28768392G>C | CA389476568 | FOXG1 | c.1113G>C (p.Glu371Asp)
| |
| 14 | g.28768392G>T | CA389476569 | FOXG1 | c.1113G>T (p.Glu371Asp)
| COSMIC |
| 14 | g.28768393A>C | CA389476572 | FOXG1 | c.1114A>C (p.Ile372Leu)
| |
| 14 | g.28768393A>G | CA389476570 | FOXG1 | c.1114A>G (p.Ile372Val)
| |
| 14 | g.28768393A>T | CA389476571 | FOXG1 | c.1114A>T (p.Ile372Phe)
| |
| 14 | g.28768394T>A | CA389476573 | FOXG1 | c.1115T>A (p.Ile372Asn)
| |
| 14 | g.28768394T>C | CA389476574 | FOXG1 | c.1115T>C (p.Ile372Thr)
| |
| 14 | g.28768394T>G | CA389476575 | FOXG1 | c.1115T>G (p.Ile372Ser)
| |
| 14 | g.28768395C>A | CA486098645 | FOXG1 | c.1116C>A (p.Ile372=)
| gnomAD v4 |
| 14 | g.28768395C>G | CA389476576 | FOXG1 | c.1116C>G (p.Ile372Met)
| |
| 14 | g.28768395C>T | CA486098647 | FOXG1 | c.1116C>T (p.Ile372=)
| |
| 14 | g.28768396C>A | CA389476577 | FOXG1 | c.1117C>A (p.Pro373Thr)
| gnomAD v4 |
| 14 | g.28768396C>G | CA389476578 | FOXG1 | c.1117C>G (p.Pro373Ala)
| |
| 14 | g.28768396C>T | CA389476579 | FOXG1 | c.1117C>T (p.Pro373Ser)
| ClinVar dbSNP gnomAD v4 |
| 14 | g.28768397C>A | CA389476580 | FOXG1 | c.1118C>A (p.Pro373Gln)
| |
| 14 | g.28768397C>G | CA389476581 | FOXG1 | c.1118C>G (p.Pro373Arg)
| |
| 14 | g.28768397C>T | CA389476582 | FOXG1 | c.1118C>T (p.Pro373Leu)
| |
| 14 | g.28768398G>A | CA7140659 | FOXG1 | c.1119G>A (p.Pro373=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.28768398G>C | CA486098662 | FOXG1 | c.1119G>C (p.Pro373=)
| |
| 14 | g.28768398G= | CA2126000398 | FOXG1 | c.1119G= (p.Pro373=)
| |
| 14 | g.28768398G>T | CA486098664 | FOXG1 | c.1119G>T (p.Pro373=)
| gnomAD v4 |
| 14 | g.28768399T>A | CA389476584 | FOXG1 | c.1120T>A (p.Tyr374Asn)
| |
| 14 | g.28768399T>C | CA389476585 | FOXG1 | c.1120T>C (p.Tyr374His)
| |
| 14 | g.28768399T>G | CA389476583 | FOXG1 | c.1120T>G (p.Tyr374Asp)
| |
| 14 | g.28768400A>C | CA389476586 | FOXG1 | c.1121A>C (p.Tyr374Ser)
| |
| 14 | g.28768400A>G | CA389476587 | FOXG1 | c.1121A>G (p.Tyr374Cys)
| gnomAD v4 |
| 14 | g.28768400A>T | CA389476588 | FOXG1 | c.1121A>T (p.Tyr374Phe)
| |
| 14 | g.28768401C>A | CA389476589 | FOXG1 | c.1122C>A (p.Tyr374Ter)
| |
| 14 | g.28768401C= | CA2126000399 | FOXG1 | c.1122C= (p.Tyr374=)
| |
| 14 | g.28768401C>G | CA389476590 | FOXG1 | c.1122C>G (p.Tyr374Ter)
| |
| 14 | g.28768401C>T | CA7140660 | FOXG1 | c.1122C>T (p.Tyr374=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.28768402G>A | CA389476591 | FOXG1 | c.1123G>A (p.Ala375Thr)
| ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.28768402G>C | CA389476592 | FOXG1 | c.1123G>C (p.Ala375Pro)
| dbSNP |
| 14 | g.28768402G= | CA2126000400 | FOXG1 | c.1123G= (p.Ala375=)
| |
| 14 | g.28768402G>T | CA389476593 | FOXG1 | c.1123G>T (p.Ala375Ser)
| |
| 14 | g.28768403C>A | CA389476594 | FOXG1 | c.1124C>A (p.Ala375Asp)
| |
| 14 | g.28768403C>G | CA389476595 | FOXG1 | c.1124C>G (p.Ala375Gly)
| |
| 14 | g.28768403C>T | CA389476596 | FOXG1 | c.1124C>T (p.Ala375Val)
| gnomAD v4 |
| 14 | g.28768404C>A | CA486098687 | FOXG1 | c.1125C>A (p.Ala375=)
| |
| 14 | g.28768404C>G | CA486098688 | FOXG1 | c.1125C>G (p.Ala375=)
| |
| 14 | g.28768404C>T | CA486098690 | FOXG1 | c.1125C>T (p.Ala375=)
| |
| 14 | g.28768405A>C | CA389476598 | FOXG1 | c.1126A>C (p.Thr376Pro)
| gnomAD v4 |
| 14 | g.28768405A>G | CA389476599 | FOXG1 | c.1126A>G (p.Thr376Ala)
| |
| 14 | g.28768405A>T | CA389476597 | FOXG1 | c.1126A>T (p.Thr376Ser)
| |
| 14 | g.28768406C>A | CA389476600 | FOXG1 | c.1127C>A (p.Thr376Lys)
| |
| 14 | g.28768406C>G | CA389476601 | FOXG1 | c.1127C>G (p.Thr376Arg)
| |
| 14 | g.28768406C>T | CA389476602 | FOXG1 | c.1127C>T (p.Thr376Met)
| COSMIC |
| 14 | g.28768407G>A | CA486098703 | FOXG1 | c.1128G>A (p.Thr376=)
| dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.28768407G>C | CA486098705 | FOXG1 | c.1128G>C (p.Thr376=)
| |
| 14 | g.28768407G= | CA2126000401 | FOXG1 | c.1128G= (p.Thr376=)
| |
| 14 | g.28768407G>T | CA486098708 | FOXG1 | c.1128G>T (p.Thr376=)
| |
| 14 | g.28768408C>A | CA389476603 | FOXG1 | c.1129C>A (p.His377Asn)
| |
| 14 | g.28768408C>G | CA389476604 | FOXG1 | c.1129C>G (p.His377Asp)
| |
| 14 | g.28768408C>T | CA389476605 | FOXG1 | c.1129C>T (p.His377Tyr)
| |
| 14 | g.28768409A>C | CA389476608 | FOXG1 | c.1130A>C (p.His377Pro)
| |
| 14 | g.28768409A>G | CA389476606 | FOXG1 | c.1130A>G (p.His377Arg)
| |
| 14 | g.28768409A>T | CA389476607 | FOXG1 | c.1130A>T (p.His377Leu)
| |
| 14 | g.28768410C>A | CA389476609 | FOXG1 | c.1131C>A (p.His377Gln)
| gnomAD v4 |
| 14 | g.28768410C>G | CA389476610 | FOXG1 | c.1131C>G (p.His377Gln)
| gnomAD v4 |
| 14 | g.28768410C>T | CA486098714 | FOXG1 | c.1131C>T (p.His377=)
| |
| 14 | g.28768411C>A | CA389476611 | FOXG1 | c.1132C>A (p.His378Asn)
| |
| 14 | g.28768411C>G | CA389476612 | FOXG1 | c.1132C>G (p.His378Asp)
| |
| 14 | g.28768411C>T | CA389476613 | FOXG1 | c.1132C>T (p.His378Tyr)
| |
| 14 | g.28768411_28768412insCCCCAA | CA2801003413 | FOXG1 | c.1132_1133insCCCCAA (p.His378delinsProProAsn)
| |
| 14 | g.28768412A= | CA2126000402 | FOXG1 | c.1133A= (p.His378=)
| |
| 14 | g.28768412A>C | CA389476614 | FOXG1 | c.1133A>C (p.His378Pro)
| dbSNP gnomAD v2 |
| 14 | g.28768412A>G | CA389476616 | FOXG1 | c.1133A>G (p.His378Arg)
| |
| 14 | g.28768412A>T | CA389476615 | FOXG1 | c.1133A>T (p.His378Leu)
| |
| 14 | g.28768412_28768413delinsAC | CA2126000403 | FOXG1 | c.1133_1134delinsAC (p.His378=)
| |
| 14 | g.28768413C>A | CA389476617 | FOXG1 | c.1134C>A (p.His378Gln)
| |
| 14 | g.28768413C>G | CA389476618 | FOXG1 | c.1134C>G (p.His378Gln)
| |
| 14 | g.28768413C>T | CA486098320 | FOXG1 | c.1134C>T (p.His378=)
| |
| 14 | g.28768414del | CA1139663431 | FOXG1 | c.1135del (p.Leu379SerfsTer6)
| ClinVar dbSNP |
