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 |
14 | g.28768413_28768414insACACCCAA | CA2801003415 | FOXG1 | c.1134_1135insACACCCAA (p.Leu379ThrfsTer9)
| |
14 | g.28768414C>A | CA389476619 | FOXG1 | c.1135C>A (p.Leu379Ile)
| |
14 | g.28768414C= | CA2126000404 | FOXG1 | c.1135C= (p.Leu379=)
| |
14 | g.28768414C>G | CA389476620 | FOXG1 | c.1135C>G (p.Leu379Val)
| dbSNP |
14 | g.28768414C>T | CA258396594 | FOXG1 | c.1135C>T (p.Leu379Phe)
| dbSNP |
14 | g.28768415T>A | CA389476623 | FOXG1 | c.1136T>A (p.Leu379His)
| |
14 | g.28768415T>C | CA389476622 | FOXG1 | c.1136T>C (p.Leu379Pro)
| |
14 | g.28768415T>G | CA389476621 | FOXG1 | c.1136T>G (p.Leu379Arg)
| |
14 | g.28768416C>A | CA486098326 | FOXG1 | c.1137C>A (p.Leu379=)
| |
14 | g.28768416C>G | CA486098328 | FOXG1 | c.1137C>G (p.Leu379=)
| |
14 | g.28768416C>T | CA486098331 | FOXG1 | c.1137C>T (p.Leu379=)
| |
14 | g.28768417A>C | CA389476624 | FOXG1 | c.1138A>C (p.Thr380Pro)
| |
14 | g.28768417A>G | CA389476625 | FOXG1 | c.1138A>G (p.Thr380Ala)
| |
14 | g.28768417A>T | CA389476626 | FOXG1 | c.1138A>T (p.Thr380Ser)
| |
14 | g.28768418C>A | CA389476627 | FOXG1 | c.1139C>A (p.Thr380Lys)
| |
14 | g.28768418C>G | CA389476628 | FOXG1 | c.1139C>G (p.Thr380Arg)
| |
14 | g.28768418C>T | CA389476629 | FOXG1 | c.1139C>T (p.Thr380Met)
| COSMIC |
14 | g.28768419G>A | CA486098334 | FOXG1 | c.1140G>A (p.Thr380=)
| dbSNP |
14 | g.28768419G>C | CA486098335 | FOXG1 | c.1140G>C (p.Thr380=)
| dbSNP gnomAD v2 gnomAD v4 |
14 | g.28768419G= | CA2126000405 | FOXG1 | c.1140G= (p.Thr380=)
| |
14 | g.28768419G>T | CA486098336 | FOXG1 | c.1140G>T (p.Thr380=)
| |
14 | g.28768420del | CA2573053901 | FOXG1 | c.1141del (p.Ala381ProfsTer4)
| ClinVar dbSNP |
14 | g.28768420G>A | CA389476630 | FOXG1 | c.1141G>A (p.Ala381Thr)
| |
14 | g.28768420G>C | CA389476632 | FOXG1 | c.1141G>C (p.Ala381Pro)
| |
14 | g.28768420G>T | CA389476631 | FOXG1 | c.1141G>T (p.Ala381Ser)
| |
14 | g.28768421C>A | CA389476633 | FOXG1 | c.1142C>A (p.Ala381Asp)
| |
14 | g.28768421C>G | CA389476634 | FOXG1 | c.1142C>G (p.Ala381Gly)
| |
14 | g.28768421C>T | CA389476635 | FOXG1 | c.1142C>T (p.Ala381Val)
| |
14 | g.28768422C>A | CA486098338 | FOXG1 | c.1143C>A (p.Ala381=)
| |
14 | g.28768422C= | CA2126000406 | FOXG1 | c.1143C= (p.Ala381=)
| |
14 | g.28768422C>G | CA7140661 | FOXG1 | c.1143C>G (p.Ala381=)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
14 | g.28768422C>T | CA486098340 | FOXG1 | c.1143C>T (p.Ala381=)
| ClinVar dbSNP COSMIC |
14 | g.28768423G>A | CA389476636 | FOXG1 | c.1144G>A (p.Ala382Thr)
| COSMIC |
14 | g.28768423G>C | CA389476637 | FOXG1 | c.1144G>C (p.Ala382Pro)
| |
14 | g.28768423G>T | CA389476638 | FOXG1 | c.1144G>T (p.Ala382Ser)
| |
14 | g.28768424C>A | CA389476639 | FOXG1 | c.1145C>A (p.Ala382Asp)
| |
14 | g.28768424C>G | CA389476640 | FOXG1 | c.1145C>G (p.Ala382Gly)
| |
14 | g.28768424C>T | CA389476641 | FOXG1 | c.1145C>T (p.Ala382Val)
| COSMIC |
14 | g.28768425C>A | CA486098341 | FOXG1 | c.1146C>A (p.Ala382=)
| |
14 | g.28768425C= | CA2126000407 | FOXG1 | c.1146C= (p.Ala382=)
| |
14 | g.28768425C>G | CA7140662 | FOXG1 | c.1146C>G (p.Ala382=)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
14 | g.28768425C>T | CA258396595 | FOXG1 | c.1146C>T (p.Ala382=)
| ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
14 | g.28768426G>A | CA7140663 | FOXG1 | c.1147G>A (p.Ala383Thr)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.28768426G>C | CA389476642 | FOXG1 | c.1147G>C (p.Ala383Pro)
| |
14 | g.28768426G= | CA2126000408 | FOXG1 | c.1147G= (p.Ala383=)
| |
14 | g.28768426G>T | CA389476643 | FOXG1 | c.1147G>T (p.Ala383Ser)
| |
14 | g.28768427C>A | CA389476644 | FOXG1 | c.1148C>A (p.Ala383Glu)
| |
14 | g.28768427C>G | CA389476645 | FOXG1 | c.1148C>G (p.Ala383Gly)
| |
14 | g.28768427C>T | CA389476646 | FOXG1 | c.1148C>T (p.Ala383Val)
| |
14 | g.28768428G>A | CA486098345 | FOXG1 | c.1149G>A (p.Ala383=)
| dbSNP gnomAD v2 gnomAD v4 |
14 | g.28768428G>C | CA7140664 | FOXG1 | c.1149G>C (p.Ala383=)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
14 | g.28768428G= | CA2126000409 | FOXG1 | c.1149G= (p.Ala383=)
| |
14 | g.28768428G>T | CA486098347 | FOXG1 | c.1149G>T (p.Ala383=)
| |
14 | g.28768429C>A | CA389476647 | FOXG1 | c.1150C>A (p.Leu384Ile)
| |
14 | g.28768429C= | CA2126000410 | FOXG1 | c.1150C= (p.Leu384=)
| |
14 | g.28768429C>G | CA389476648 | FOXG1 | c.1150C>G (p.Leu384Val)
| |
14 | g.28768429C>T | CA7140665 | FOXG1 | c.1150C>T (p.Leu384=)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
14 | g.28768430T>A | CA389476649 | FOXG1 | c.1151T>A (p.Leu384Gln)
| |
14 | g.28768430T>C | CA389476650 | FOXG1 | c.1151T>C (p.Leu384Pro)
| |
14 | g.28768430T>G | CA389476651 | FOXG1 | c.1151T>G (p.Leu384Arg)
| |
14 | g.28768431A= | CA2126000411 | FOXG1 | c.1152A= (p.Leu384=)
| |
14 | g.28768431A>C | CA486098350 | FOXG1 | c.1152A>C (p.Leu384=)
| COSMIC |
14 | g.28768431A>G | CA486098352 | FOXG1 | c.1152A>G (p.Leu384=)
| ClinVar dbSNP gnomAD v2 gnomAD v4 |
14 | g.28768431A>T | CA486098354 | FOXG1 | c.1152A>T (p.Leu384=)
| |
14 | g.28768432G>A | CA389476652 | FOXG1 | c.1153G>A (p.Ala385Thr)
| |
14 | g.28768432G>C | CA389476653 | FOXG1 | c.1153G>C (p.Ala385Pro)
| COSMIC |
14 | g.28768432G>T | CA389476654 | FOXG1 | c.1153G>T (p.Ala385Ser)
| |
14 | g.28768433C>A | CA389476657 | FOXG1 | c.1154C>A (p.Ala385Asp)
| |
14 | g.28768433C= | CA2126000412 | FOXG1 | c.1154C= (p.Ala385=)
| |
14 | g.28768433C>G | CA389476655 | FOXG1 | c.1154C>G (p.Ala385Gly)
| dbSNP |
14 | g.28768433C>T | CA389476656 | FOXG1 | c.1154C>T (p.Ala385Val)
| |
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=)
| |