UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 14 | g.28768346_28768348del | CA2126000380 | FOXG1 | c.1067_1069del (p.Phe356del) | dbSNP gnomAD v4 |
| 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=) | |
| 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) |