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New user registrations, changes to existing user profiles, and changes to user credentials will be suspended for several weeks.
This allows us to avoid multi-day, broad service outages as we continue to migrate off our current cloud hosting provider.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 14 | g.28768374_28768393del | CA2573053900 | FOXG1 | c.1095_1114del (p.Arg366ProfsTer?) | ClinVar dbSNP |
| 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?) | |
| 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.28768399_28768435del | CA2832528763 | FOXG1 | c.1120_1156del (p.Tyr374ProfsTer?) | |
| 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) | |
| 14 | g.28768449C>A | CA389476686 | FOXG1 | c.1170C>A (p.Cys390Ter) | ClinVar dbSNP |
| 14 | g.28768449C= | CA2126000420 | FOXG1 | c.1170C= (p.Cys390=) | |
| 14 | g.28768449C>G | CA389476687 | FOXG1 | c.1170C>G (p.Cys390Trp) | |
| 14 | g.28768449C>T | CA486098376 | FOXG1 | c.1170C>T (p.Cys390=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28768450G>A | CA389476690 | FOXG1 | c.1171G>A (p.Gly391Ser) | |
| 14 | g.28768450G>C | CA389476688 | FOXG1 | c.1171G>C (p.Gly391Arg) | |
| 14 | g.28768450G>T | CA389476689 | FOXG1 | c.1171G>T (p.Gly391Cys) | |
| 14 | g.28768451G>A | CA389476691 | FOXG1 | c.1172G>A (p.Gly391Asp) | dbSNP |
| 14 | g.28768451G>C | CA389476692 | FOXG1 | c.1172G>C (p.Gly391Ala) | |
| 14 | g.28768451G= | CA2126000421 | FOXG1 | c.1172G= (p.Gly391=) | |
| 14 | g.28768451G>T | CA389476693 | FOXG1 | c.1172G>T (p.Gly391Val) | dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.28768452C>A | CA486098377 | FOXG1 | c.1173C>A (p.Gly391=) | |
| 14 | g.28768452C= | CA2126000422 | FOXG1 | c.1173C= (p.Gly391=) | |
| 14 | g.28768452C>G | CA486098378 | FOXG1 | c.1173C>G (p.Gly391=) | |
| 14 | g.28768452C>T | CA486098379 | FOXG1 | c.1173C>T (p.Gly391=) | ClinVar dbSNP gnomAD v4 |
| 14 | g.28768453C>A | CA389476694 | FOXG1 | c.1174C>A (p.Leu392Met) | COSMIC |
| 14 | g.28768453C= | CA2126000423 | FOXG1 | c.1174C= (p.Leu392=) | |
| 14 | g.28768453C>G | CA389476695 | FOXG1 | c.1174C>G (p.Leu392Val) | |
| 14 | g.28768453C>T | CA486098380 | FOXG1 | c.1174C>T (p.Leu392=) | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.28768454T>A | CA389476698 | FOXG1 | c.1175T>A (p.Leu392Gln) | |
| 14 | g.28768454T>C | CA389476697 | FOXG1 | c.1175T>C (p.Leu392Pro) | |
| 14 | g.28768454T>G | CA389476696 | FOXG1 | c.1175T>G (p.Leu392Arg) | |
| 14 | g.28768455G>A | CA486098381 | FOXG1 | c.1176G>A (p.Leu392=) | gnomAD v4 |
| 14 | g.28768455G>C | CA486098385 | FOXG1 | c.1176G>C (p.Leu392=) | |
| 14 | g.28768455G>T | CA486098383 | FOXG1 | c.1176G>T (p.Leu392=) | |
| 14 | g.28768456T>A | CA389476699 | FOXG1 | c.1177T>A (p.Ser393Thr) | |
| 14 | g.28768456T>C | CA389476700 | FOXG1 | c.1177T>C (p.Ser393Pro) | |
| 14 | g.28768456T>G | CA389476701 | FOXG1 | c.1177T>G (p.Ser393Ala) | |
| 14 | g.28768457C>A | CA389476702 | FOXG1 | c.1178C>A (p.Ser393Ter) | |
| 14 | g.28768457C= | CA2126000424 | FOXG1 | c.1178C= (p.Ser393=) | |
| 14 | g.28768457C>G | CA389476703 | FOXG1 | c.1178C>G (p.Ser393Trp) | ClinVar dbSNP |
| 14 | g.28768457C>T | CA389476704 | FOXG1 | c.1178C>T (p.Ser393Leu) | |
| 14 | g.28768458G>A | CA486098387 | FOXG1 | c.1179G>A (p.Ser393=) | |
| 14 | g.28768458G>C | CA486098388 | FOXG1 | c.1179G>C (p.Ser393=) | ClinVar dbSNP |
| 14 | g.28768458G>T | CA486098390 | FOXG1 | c.1179G>T (p.Ser393=) | |
| 14 | g.28768459G>A | CA389476705 | FOXG1 | c.1180G>A (p.Val394Met) | |
| 14 | g.28768459G>C | CA389476706 | FOXG1 | c.1180G>C (p.Val394Leu) | |
| 14 | g.28768459G>T | CA389476707 | FOXG1 | c.1180G>T (p.Val394Leu) | |
| 14 | g.28768460T>A | CA389476708 | FOXG1 | c.1181T>A (p.Val394Glu) | |
| 14 | g.28768460T>C | CA389476709 | FOXG1 | c.1181T>C (p.Val394Ala) | |
| 14 | g.28768460T>G | CA389476710 | FOXG1 | c.1181T>G (p.Val394Gly) | ClinVar dbSNP gnomAD v4 |
| 14 | g.28768460T= | CA2126000425 | FOXG1 | c.1181T= (p.Val394=) | |
| 14 | g.28768461G>A | CA486098393 | FOXG1 | c.1182G>A (p.Val394=) | dbSNP gnomAD v4 |
| 14 | g.28768461G>C | CA486098394 | FOXG1 | c.1182G>C (p.Val394=) | |
| 14 | g.28768461G= | CA2126000426 | FOXG1 | c.1182G= (p.Val394=) | |
| 14 | g.28768461G>T | CA7140668 | FOXG1 | c.1182G>T (p.Val394=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.28768462C>A | CA389476713 | FOXG1 | c.1183C>A (p.Pro395Thr) | |
| 14 | g.28768462C>G | CA389476711 | FOXG1 | c.1183C>G (p.Pro395Ala) | |
| 14 | g.28768462C>T | CA389476712 | FOXG1 | c.1183C>T (p.Pro395Ser) | gnomAD v4 |
| 14 | g.28768463C>A | CA389476714 | FOXG1 | c.1184C>A (p.Pro395His) | |
| 14 | g.28768463C= | CA2126000427 | FOXG1 | c.1184C= (p.Pro395=) | |
| 14 | g.28768463C>G | CA389476715 | FOXG1 | c.1184C>G (p.Pro395Arg) | |
| 14 | g.28768463C>T | CA389476716 | FOXG1 | c.1184C>T (p.Pro395Leu) | dbSNP gnomAD v2 |
| 14 | g.28768464C>A | CA486098397 | FOXG1 | c.1185C>A (p.Pro395=) | |
| 14 | g.28768464C= | CA2126000428 | FOXG1 | c.1185C= (p.Pro395=) | |
| 14 | g.28768464C>G | CA486098398 | FOXG1 | c.1185C>G (p.Pro395=) | gnomAD v4 |
| 14 | g.28768464C>T | CA486098399 | FOXG1 | c.1185C>T (p.Pro395=) | dbSNP |
| 14 | g.28768465T>A | CA389476717 | FOXG1 | c.1186T>A (p.Cys396Ser) | ClinVar dbSNP |
| 14 | g.28768465T>C | CA389476718 | FOXG1 | c.1186T>C (p.Cys396Arg) | |
| 14 | g.28768465T>G | CA389476719 | FOXG1 | c.1186T>G (p.Cys396Gly) | |
| 14 | g.28768465T= | CA2126000429 | FOXG1 | c.1186T= (p.Cys396=) | |
| 14 | g.28768466G>A | CA389476720 | FOXG1 | c.1187G>A (p.Cys396Tyr) | gnomAD v4 |
| 14 | g.28768466G>C | CA389476721 | FOXG1 | c.1187G>C (p.Cys396Ser) | |
| 14 | g.28768466G>T | CA389476722 | FOXG1 | c.1187G>T (p.Cys396Phe) | |
| 14 | g.28768467C>A | CA389476723 | FOXG1 | c.1188C>A (p.Cys396Ter) | |
| 14 | g.28768467C= | CA2126000430 | FOXG1 | c.1188C= (p.Cys396=) | |
| 14 | g.28768467C>G | CA389476724 | FOXG1 | c.1188C>G (p.Cys396Trp) | |
| 14 | g.28768467C>T | CA7140669 | FOXG1 | c.1188C>T (p.Cys396=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 14 | g.28768468T>A | CA389476727 | FOXG1 | c.1189T>A (p.Ser397Thr) | |
| 14 | g.28768468T>C | CA389476726 | FOXG1 | c.1189T>C (p.Ser397Pro) | |
| 14 | g.28768468T>G | CA389476725 | FOXG1 | c.1189T>G (p.Ser397Ala) | |
| 14 | g.28768469C>A | CA389476728 | FOXG1 | c.1190C>A (p.Ser397Tyr) | |
| 14 | g.28768469C= | CA2126000431 | FOXG1 | c.1190C= (p.Ser397=) | |
| 14 | g.28768469C>G | CA389476729 | FOXG1 | c.1190C>G (p.Ser397Cys) | |
| 14 | g.28768469C>T | CA16607642 | FOXG1 | c.1190C>T (p.Ser397Phe) | ClinVar dbSNP |
| 14 | g.28768470T>A | CA486098405 | FOXG1 | c.1191T>A (p.Ser397=) | |
| 14 | g.28768470T>C | CA486098406 | FOXG1 | c.1191T>C (p.Ser397=) | dbSNP gnomAD v2 COSMIC |
| 14 | g.28768470T>G | CA486098407 | FOXG1 | c.1191T>G (p.Ser397=) | |
| 14 | g.28768470T= | CA2126000432 | FOXG1 | c.1191T= (p.Ser397=) | |
| 14 | g.28768471G>A | CA389476730 | FOXG1 | c.1192G>A (p.Gly398Arg) | |
| 14 | g.28768471G>C | CA389476732 | FOXG1 | c.1192G>C (p.Gly398Arg) | |
| 14 | g.28768471G>T | CA389476731 | FOXG1 | c.1192G>T (p.Gly398Trp) | |
| 14 | g.28768472G>A | CA389476733 | FOXG1 | c.1193G>A (p.Gly398Glu) | |
| 14 | g.28768472G>C | CA389476734 | FOXG1 | c.1193G>C (p.Gly398Ala) | dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.28768472G= | CA2126000433 | FOXG1 | c.1193G= (p.Gly398=) | |
| 14 | g.28768472G>T | CA389476735 | FOXG1 | c.1193G>T (p.Gly398Val) | |
| 14 | g.28768473G>A | CA486098409 | FOXG1 | c.1194G>A (p.Gly398=) | gnomAD v4 |
| 14 | g.28768473G>C | CA486098410 | FOXG1 | c.1194G>C (p.Gly398=) | |
| 14 | g.28768473G>T | CA486098411 | FOXG1 | c.1194G>T (p.Gly398=) | |
| 14 | g.28768474A= | CA2126000434 | FOXG1 | c.1195A= (p.Thr399=) | |
| 14 | g.28768474A>C | CA389476736 | FOXG1 | c.1195A>C (p.Thr399Pro) | |
| 14 | g.28768474A>G | CA389476737 | FOXG1 | c.1195A>G (p.Thr399Ala) | |
| 14 | g.28768474A>T | CA7140670 | FOXG1 | c.1195A>T (p.Thr399Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.28768475C>A | CA389476738 | FOXG1 | c.1196C>A (p.Thr399Asn) | |
| 14 | g.28768475C>G | CA389476739 | FOXG1 | c.1196C>G (p.Thr399Ser) | |
| 14 | g.28768475C>T | CA389476740 | FOXG1 | c.1196C>T (p.Thr399Ile) | |
| 14 | g.28768476C>A | CA486098415 | FOXG1 | c.1197C>A (p.Thr399=) | |
| 14 | g.28768476C>G | CA486098413 | FOXG1 | c.1197C>G (p.Thr399=) | |
| 14 | g.28768476C>T | CA486098414 | FOXG1 | c.1197C>T (p.Thr399=) | gnomAD v4 |
| 14 | g.28768477T>A | CA389476741 | FOXG1 | c.1198T>A (p.Tyr400Asn) | |
| 14 | g.28768477T>C | CA389476742 | FOXG1 | c.1198T>C (p.Tyr400His) | |
| 14 | g.28768477T>G | CA389476743 | FOXG1 | c.1198T>G (p.Tyr400Asp) | |
| 14 | g.28768478A>C | CA389476746 | FOXG1 | c.1199A>C (p.Tyr400Ser) | |
| 14 | g.28768478A>G | CA389476745 | FOXG1 | c.1199A>G (p.Tyr400Cys) | |
| 14 | g.28768478A>T | CA389476744 | FOXG1 | c.1199A>T (p.Tyr400Phe) | |
| 14 | g.28768479C>A | CA235611 | FOXG1 | c.1200C>A (p.Tyr400Ter) | ClinVar dbSNP |
| 14 | g.28768479C= | CA2126000435 | FOXG1 | c.1200C= (p.Tyr400=) | |
| 14 | g.28768479C>G | CA123557 | FOXG1 | c.1200C>G (p.Tyr400Ter) | ClinVar dbSNP |
| 14 | g.28768479C>T | CA7140671 | FOXG1 | c.1200C>T (p.Tyr400=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28768480T>A | CA389476747 | FOXG1 | c.1201T>A (p.Ser401Thr) | |
| 14 | g.28768480T>C | CA389476748 | FOXG1 | c.1201T>C (p.Ser401Pro) | |
| 14 | g.28768480T>G | CA389476749 | FOXG1 | c.1201T>G (p.Ser401Ala) | |
| 14 | g.28768481C>A | CA389476750 | FOXG1 | c.1202C>A (p.Ser401Tyr) | |
| 14 | g.28768481C>G | CA389476751 | FOXG1 | c.1202C>G (p.Ser401Cys) | |
| 14 | g.28768481C>T | CA389476752 | FOXG1 | c.1202C>T (p.Ser401Phe) | COSMIC |
| 14 | g.28768482C>A | CA486098418 | FOXG1 | c.1203C>A (p.Ser401=) | |
| 14 | g.28768482C= | CA2126000436 | FOXG1 | c.1203C= (p.Ser401=) | |
| 14 | g.28768482C>G | CA486098422 | FOXG1 | c.1203C>G (p.Ser401=) | |
| 14 | g.28768482C>T | CA7140672 | FOXG1 | c.1203C>T (p.Ser401=) | ClinVar dbSNP ExAC gnomAD v3 gnomAD v4 |
| 14 | g.28768483C>A | CA389476753 | FOXG1 | c.1204C>A (p.Leu402Ile) | |
| 14 | g.28768483C>G | CA389476754 | FOXG1 | c.1204C>G (p.Leu402Val) | |
| 14 | g.28768483C>T | CA389476755 | FOXG1 | c.1204C>T (p.Leu402Phe) | COSMIC |
| 14 | g.28768484T>A | CA389476757 | FOXG1 | c.1205T>A (p.Leu402His) | |
| 14 | g.28768484T>C | CA389476758 | FOXG1 | c.1205T>C (p.Leu402Pro) | |
| 14 | g.28768484T>G | CA389476756 | FOXG1 | c.1205T>G (p.Leu402Arg) | |
| 14 | g.28768485C>A | CA486098424 | FOXG1 | c.1206C>A (p.Leu402=) | |
| 14 | g.28768485C= | CA2126000437 | FOXG1 | c.1206C= (p.Leu402=) | |
| 14 | g.28768485C>G | CA486098425 | FOXG1 | c.1206C>G (p.Leu402=) | |
| 14 | g.28768485C>T | CA486098426 | FOXG1 | c.1206C>T (p.Leu402=) | dbSNP |
| 14 | g.28768486A>C | CA389476759 | FOXG1 | c.1207A>C (p.Asn403His) | |
| 14 | g.28768486A>G | CA389476760 | FOXG1 | c.1207A>G (p.Asn403Asp) | |
| 14 | g.28768486A>T | CA389476761 | FOXG1 | c.1207A>T (p.Asn403Tyr) | |
| 14 | g.28768487A= | CA2126000438 | FOXG1 | c.1208A= (p.Asn403=) | |
| 14 | g.28768487A>C | CA389476762 | FOXG1 | c.1208A>C (p.Asn403Thr) | |
| 14 | g.28768487A>G | CA258396598 | FOXG1 | c.1208A>G (p.Asn403Ser) | ClinVar dbSNP gnomAD v4 |
| 14 | g.28768487A>T | CA389476763 | FOXG1 | c.1208A>T (p.Asn403Ile) |