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.28768261_28768268dup | CA915948879 | FOXG1 | c.982_989dup (p.Ser332AlafsTer17) | ClinVar dbSNP |
| 14 | g.28768262_28768270dup | CA2590338603 | FOXG1 | c.983_991dup (p.Thr330_Thr331insAsnGlyThr) | gnomAD v3 gnomAD v4 |
| 14 | g.28768261_28768264dup | CA2739291838 | FOXG1 | c.982_985dup (p.Gly329GlufsTer?) | |
| 14 | g.28768264G>A | CA389476288 | FOXG1 | c.985G>A (p.Gly329Ser) | gnomAD v4 |
| 14 | g.28768264G>C | CA389476289 | FOXG1 | c.985G>C (p.Gly329Arg) | dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.28768264G= | CA2126000346 | FOXG1 | c.985G= (p.Gly329=) | |
| 14 | g.28768264G>T | CA389476290 | FOXG1 | c.985G>T (p.Gly329Cys) | gnomAD v4 |
| 14 | g.28768265G>A | CA389476291 | FOXG1 | c.986G>A (p.Gly329Asp) | dbSNP |
| 14 | g.28768265G>C | CA389476292 | FOXG1 | c.986G>C (p.Gly329Ala) | |
| 14 | g.28768265G= | CA2126000347 | FOXG1 | c.986G= (p.Gly329=) | |
| 14 | g.28768265G>T | CA389476293 | FOXG1 | c.986G>T (p.Gly329Val) | gnomAD v4 COSMIC |
| 14 | g.28768266C>A | CA486098382 | FOXG1 | c.987C>A (p.Gly329=) | |
| 14 | g.28768266C= | CA2126000348 | FOXG1 | c.987C= (p.Gly329=) | |
| 14 | g.28768266C>G | CA486098384 | FOXG1 | c.987C>G (p.Gly329=) | COSMIC |
| 14 | g.28768266C>T | CA486098386 | FOXG1 | c.987C>T (p.Gly329=) | dbSNP |
| 14 | g.28768267A>C | CA389476294 | FOXG1 | c.988A>C (p.Thr330Pro) | gnomAD v4 |
| 14 | g.28768267A>G | CA389476295 | FOXG1 | c.988A>G (p.Thr330Ala) | |
| 14 | g.28768267A>T | CA389476296 | FOXG1 | c.988A>T (p.Thr330Ser) | |
| 14 | g.28768268C>A | CA389476297 | FOXG1 | c.989C>A (p.Thr330Asn) | dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 14 | g.28768268C= | CA2126000349 | FOXG1 | c.989C= (p.Thr330=) | |
| 14 | g.28768268C>G | CA258396588 | FOXG1 | c.989C>G (p.Thr330Ser) | dbSNP |
| 14 | g.28768268C>T | CA389476298 | FOXG1 | c.989C>T (p.Thr330Ile) | |
| 14 | g.28768269C>A | CA486098392 | FOXG1 | c.990C>A (p.Thr330=) | |
| 14 | g.28768269C>G | CA486098389 | FOXG1 | c.990C>G (p.Thr330=) | |
| 14 | g.28768269C>T | CA486098391 | FOXG1 | c.990C>T (p.Thr330=) | COSMIC |
| 14 | g.28768270A= | CA2126000350 | FOXG1 | c.991A= (p.Thr331=) | |
| 14 | g.28768270A>C | CA389476300 | FOXG1 | c.991A>C (p.Thr331Pro) | |
| 14 | g.28768270A>G | CA7140645 | FOXG1 | c.991A>G (p.Thr331Ala) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28768270A>T | CA389476299 | FOXG1 | c.991A>T (p.Thr331Ser) | |
| 14 | g.28768271C>A | CA389476301 | FOXG1 | c.992C>A (p.Thr331Lys) | |
| 14 | g.28768271C>G | CA389476302 | FOXG1 | c.992C>G (p.Thr331Arg) | |
| 14 | g.28768271C>T | CA389476303 | FOXG1 | c.992C>T (p.Thr331Met) | |
| 14 | g.28768272G>A | CA7140646 | FOXG1 | c.993G>A (p.Thr331=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.28768272G>C | CA486098395 | FOXG1 | c.993G>C (p.Thr331=) | |
| 14 | g.28768272G= | CA2126000351 | FOXG1 | c.993G= (p.Thr331=) | |
| 14 | g.28768272G>T | CA486098396 | FOXG1 | c.993G>T (p.Thr331=) | gnomAD v4 |
| 14 | g.28768273T>A | CA389476305 | FOXG1 | c.994T>A (p.Ser332Thr) | |
| 14 | g.28768273T>C | CA389476304 | FOXG1 | c.994T>C (p.Ser332Pro) | |
| 14 | g.28768273T>G | CA7140647 | FOXG1 | c.994T>G (p.Ser332Ala) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 14 | g.28768273T= | CA2126000352 | FOXG1 | c.994T= (p.Ser332=) | |
| 14 | g.28768274del | CA2739277846 | FOXG1 | c.995del (p.Ser332TrpfsTer14) | ClinVar |
| 14 | g.28768274C>A | CA389476306 | FOXG1 | c.995C>A (p.Ser332Ter) | gnomAD v3 gnomAD v4 |
| 14 | g.28768274C>G | CA389476307 | FOXG1 | c.995C>G (p.Ser332Trp) | |
| 14 | g.28768274C>T | CA389476308 | FOXG1 | c.995C>T (p.Ser332Leu) | COSMIC |
| 14 | g.28768275G>A | CA486098400 | FOXG1 | c.996G>A (p.Ser332=) | COSMIC |
| 14 | g.28768275G>C | CA486098401 | FOXG1 | c.996G>C (p.Ser332=) | |
| 14 | g.28768275G>T | CA486098402 | FOXG1 | c.996G>T (p.Ser332=) | |
| 14 | g.28768276G>A | CA389476309 | FOXG1 | c.997G>A (p.Ala333Thr) | |
| 14 | g.28768276G>C | CA389476310 | FOXG1 | c.997G>C (p.Ala333Pro) | |
| 14 | g.28768276G>T | CA389476311 | FOXG1 | c.997G>T (p.Ala333Ser) | |
| 14 | g.28768277C>A | CA389476312 | FOXG1 | c.998C>A (p.Ala333Asp) | |
| 14 | g.28768277C= | CA2126000353 | FOXG1 | c.998C= (p.Ala333=) | |
| 14 | g.28768277C>G | CA389476314 | FOXG1 | c.998C>G (p.Ala333Gly) | |
| 14 | g.28768277C>T | CA389476313 | FOXG1 | c.998C>T (p.Ala333Val) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.28768278C>A | CA486098403 | FOXG1 | c.999C>A (p.Ala333=) | |
| 14 | g.28768278C= | CA2126000354 | FOXG1 | c.999C= (p.Ala333=) | |
| 14 | g.28768278C>G | CA486098404 | FOXG1 | c.999C>G (p.Ala333=) | |
| 14 | g.28768278C>T | CA7140648 | FOXG1 | c.999C>T (p.Ala333=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.28768279T>A | CA389476317 | FOXG1 | c.1000T>A (p.Tyr334Asn) | |
| 14 | g.28768279T>C | CA389476315 | FOXG1 | c.1000T>C (p.Tyr334His) | |
| 14 | g.28768279T>G | CA389476316 | FOXG1 | c.1000T>G (p.Tyr334Asp) | |
| 14 | g.28768280A>C | CA389476318 | FOXG1 | c.1001A>C (p.Tyr334Ser) | |
| 14 | g.28768280A>G | CA389476319 | FOXG1 | c.1001A>G (p.Tyr334Cys) | ClinVar dbSNP |
| 14 | g.28768280A>T | CA389476320 | FOXG1 | c.1001A>T (p.Tyr334Phe) | |
| 14 | g.28768281C>A | CA389476321 | FOXG1 | c.1002C>A (p.Tyr334Ter) | COSMIC |
| 14 | g.28768281C>G | CA389476322 | FOXG1 | c.1002C>G (p.Tyr334Ter) | |
| 14 | g.28768281C>T | CA486098408 | FOXG1 | c.1002C>T (p.Tyr334=) | |
| 14 | g.28768281_28768282delinsAG | CA645570796 | FOXG1 | c.1002_1003delinsAG (p.Tyr334Ter) | COSMIC |
| 14 | g.28768282C>A | CA389476323 | FOXG1 | c.1003C>A (p.Pro335Thr) | |
| 14 | g.28768282C= | CA2126000355 | FOXG1 | c.1003C= (p.Pro335=) | |
| 14 | g.28768282C>G | CA258396589 | FOXG1 | c.1003C>G (p.Pro335Ala) | dbSNP COSMIC |
| 14 | g.28768282C>T | CA389476324 | FOXG1 | c.1003C>T (p.Pro335Ser) | ClinVar gnomAD v4 |
| 14 | g.28768283C>A | CA389476325 | FOXG1 | c.1004C>A (p.Pro335His) | |
| 14 | g.28768283C>G | CA389476326 | FOXG1 | c.1004C>G (p.Pro335Arg) | |
| 14 | g.28768283C>T | CA389476327 | FOXG1 | c.1004C>T (p.Pro335Leu) | |
| 14 | g.28768284C>A | CA486098412 | FOXG1 | c.1005C>A (p.Pro335=) | |
| 14 | g.28768284C= | CA2126000356 | FOXG1 | c.1005C= (p.Pro335=) | |
| 14 | g.28768284C>G | CA258396590 | FOXG1 | c.1005C>G (p.Pro335=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.28768284C>T | CA258396591 | FOXG1 | c.1005C>T (p.Pro335=) | dbSNP gnomAD v4 |
| 14 | g.28768285A= | CA2126000357 | FOXG1 | c.1006A= (p.Ser336=) | |
| 14 | g.28768285A>C | CA389476328 | FOXG1 | c.1006A>C (p.Ser336Arg) | |
| 14 | g.28768285A>G | CA389476330 | FOXG1 | c.1006A>G (p.Ser336Gly) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.28768285A>T | CA389476329 | FOXG1 | c.1006A>T (p.Ser336Cys) | |
| 14 | g.28768286G>A | CA389476331 | FOXG1 | c.1007G>A (p.Ser336Asn) | |
| 14 | g.28768286G>C | CA389476332 | FOXG1 | c.1007G>C (p.Ser336Thr) | |
| 14 | g.28768286G= | CA2126000358 | FOXG1 | c.1007G= (p.Ser336=) | |
| 14 | g.28768286G>T | CA389476333 | FOXG1 | c.1007G>T (p.Ser336Ile) | gnomAD v4 |
| 14 | g.28768286dup | CA913203528 | FOXG1 | c.1007dup (p.Ser336ArgfsTer?) | ClinVar |
| 14 | g.28768287C>A | CA389476334 | FOXG1 | c.1008C>A (p.Ser336Arg) | COSMIC |
| 14 | g.28768287C= | CA2126000359 | FOXG1 | c.1008C= (p.Ser336=) | |
| 14 | g.28768287C>G | CA389476335 | FOXG1 | c.1008C>G (p.Ser336Arg) | gnomAD v4 |
| 14 | g.28768287C>T | CA486098416 | FOXG1 | c.1008C>T (p.Ser336=) | dbSNP |
| 14 | g.28768290_28768294dup | CA1139663429 | FOXG1 | c.1011_1015dup (p.Met339ThrfsTer9) | ClinVar dbSNP |
| 14 | g.28768288C>A | CA389476336 | FOXG1 | c.1009C>A (p.His337Asn) | COSMIC |
| 14 | g.28768288C>G | CA389476337 | FOXG1 | c.1009C>G (p.His337Asp) | |
| 14 | g.28768288C>T | CA389476338 | FOXG1 | c.1009C>T (p.His337Tyr) | |
| 14 | g.28768289A= | CA2126000360 | FOXG1 | c.1010A= (p.His337=) | |
| 14 | g.28768289A>C | CA389476339 | FOXG1 | c.1010A>C (p.His337Pro) | |
| 14 | g.28768289A>G | CA389476340 | FOXG1 | c.1010A>G (p.His337Arg) | |
| 14 | g.28768289A>T | CA389476341 | FOXG1 | c.1010A>T (p.His337Leu) | |
| 14 | g.28768290C>A | CA389476342 | FOXG1 | c.1011C>A (p.His337Gln) | |
| 14 | g.28768290C= | CA2126000361 | FOXG1 | c.1011C= (p.His337=) | |
| 14 | g.28768290C>G | CA389476343 | FOXG1 | c.1011C>G (p.His337Gln) | |
| 14 | g.28768290C>T | CA486098417 | FOXG1 | c.1011C>T (p.His337=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28768293dup | CA916083365 | FOXG1 | c.1014dup (p.Met339HisfsTer?) | ClinVar dbSNP |
| 14 | g.28768291C>A | CA389476344 | FOXG1 | c.1012C>A (p.Pro338Thr) | gnomAD v4 |
| 14 | g.28768291C>G | CA389476345 | FOXG1 | c.1012C>G (p.Pro338Ala) | |
| 14 | g.28768291C>T | CA389476346 | FOXG1 | c.1012C>T (p.Pro338Ser) | COSMIC |
| 14 | g.28768292C>A | CA389476347 | FOXG1 | c.1013C>A (p.Pro338His) | gnomAD v4 |
| 14 | g.28768292C>G | CA389476348 | FOXG1 | c.1013C>G (p.Pro338Arg) | |
| 14 | g.28768292C>T | CA389476349 | FOXG1 | c.1013C>T (p.Pro338Leu) | |
| 14 | g.28768293C>A | CA486098419 | FOXG1 | c.1014C>A (p.Pro338=) | |
| 14 | g.28768293C>G | CA486098420 | FOXG1 | c.1014C>G (p.Pro338=) | |
| 14 | g.28768293C>T | CA486098421 | FOXG1 | c.1014C>T (p.Pro338=) | gnomAD v4 |
| 14 | g.28768294A>C | CA389476350 | FOXG1 | c.1015A>C (p.Met339Leu) | |
| 14 | g.28768294A>G | CA389476351 | FOXG1 | c.1015A>G (p.Met339Val) | |
| 14 | g.28768294A>T | CA389476352 | FOXG1 | c.1015A>T (p.Met339Leu) | |
| 14 | g.28768295T>A | CA389476353 | FOXG1 | c.1016T>A (p.Met339Lys) | |
| 14 | g.28768295T>C | CA389476354 | FOXG1 | c.1016T>C (p.Met339Thr) | |
| 14 | g.28768295T>G | CA389476355 | FOXG1 | c.1016T>G (p.Met339Arg) | |
| 14 | g.28768296G>A | CA389476358 | FOXG1 | c.1017G>A (p.Met339Ile) | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.28768296G>C | CA389476357 | FOXG1 | c.1017G>C (p.Met339Ile) | |
| 14 | g.28768296G= | CA2126000362 | FOXG1 | c.1017G= (p.Met339=) | |
| 14 | g.28768296G>T | CA389476356 | FOXG1 | c.1017G>T (p.Met339Ile) | gnomAD v4 |
| 14 | g.28768297C>A | CA389476359 | FOXG1 | c.1018C>A (p.Pro340Thr) | |
| 14 | g.28768297C= | CA2126000363 | FOXG1 | c.1018C= (p.Pro340=) | |
| 14 | g.28768297C>G | CA389476360 | FOXG1 | c.1018C>G (p.Pro340Ala) | |
| 14 | g.28768297C>T | CA389476361 | FOXG1 | c.1018C>T (p.Pro340Ser) | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.28768299del | CA2573149904 | FOXG1 | c.1020del (p.Tyr341ThrfsTer5) | ClinVar dbSNP |
| 14 | g.28768298C>A | CA389476362 | FOXG1 | c.1019C>A (p.Pro340His) | COSMIC |
| 14 | g.28768298C>G | CA389476363 | FOXG1 | c.1019C>G (p.Pro340Arg) | gnomAD v4 |
| 14 | g.28768298C>T | CA389476364 | FOXG1 | c.1019C>T (p.Pro340Leu) | |
| 14 | g.28768300_28768308del | CA2741363690 | FOXG1 | c.1021_1029del (p.Tyr341_Ser343del) | |
| 14 | g.28768299C>A | CA486098428 | FOXG1 | c.1020C>A (p.Pro340=) | |
| 14 | g.28768299C>G | CA486098429 | FOXG1 | c.1020C>G (p.Pro340=) | |
| 14 | g.28768299C>T | CA486098430 | FOXG1 | c.1020C>T (p.Pro340=) | ClinVar dbSNP |
| 14 | g.28768300T>A | CA389476365 | FOXG1 | c.1021T>A (p.Tyr341Asn) | |
| 14 | g.28768300T>C | CA389476366 | FOXG1 | c.1021T>C (p.Tyr341His) | |
| 14 | g.28768300T>G | CA389476367 | FOXG1 | c.1021T>G (p.Tyr341Asp) | |
| 14 | g.28768300dup | CA658770580 | FOXG1 | c.1021dup (p.Tyr341LeufsTer?) | |
| 14 | g.28768301A>C | CA389476368 | FOXG1 | c.1022A>C (p.Tyr341Ser) | |
| 14 | g.28768301A>G | CA389476369 | FOXG1 | c.1022A>G (p.Tyr341Cys) | |
| 14 | g.28768301A>T | CA389476370 | FOXG1 | c.1022A>T (p.Tyr341Phe) | |
| 14 | g.28768302C>A | CA389476371 | FOXG1 | c.1023C>A (p.Tyr341Ter) | |
| 14 | g.28768302C= | CA2126000364 | FOXG1 | c.1023C= (p.Tyr341=) | |
| 14 | g.28768302C>G | CA389476372 | FOXG1 | c.1023C>G (p.Tyr341Ter) | ClinVar dbSNP |
| 14 | g.28768302C>T | CA7140649 | FOXG1 | c.1023C>T (p.Tyr341=) | dbSNP ExAC gnomAD v2 |
| 14 | g.28768303A= | CA2126000365 | FOXG1 | c.1024A= (p.Ser342=) | |
| 14 | g.28768303A>C | CA389476373 | FOXG1 | c.1024A>C (p.Ser342Arg) | |
| 14 | g.28768303A>G | CA389476375 | FOXG1 | c.1024A>G (p.Ser342Gly) | dbSNP gnomAD v4 |
| 14 | g.28768303A>T | CA389476374 | FOXG1 | c.1024A>T (p.Ser342Cys) | |
| 14 | g.28768304G>A | CA389476376 | FOXG1 | c.1025G>A (p.Ser342Asn) | |
| 14 | g.28768304G>C | CA389476378 | FOXG1 | c.1025G>C (p.Ser342Thr) | |
| 14 | g.28768304G>T | CA389476377 | FOXG1 | c.1025G>T (p.Ser342Ile) | |
| 14 | g.28768305C>A | CA389476379 | FOXG1 | c.1026C>A (p.Ser342Arg) | |
| 14 | g.28768305C= | CA2126000366 | FOXG1 | c.1026C= (p.Ser342=) | |
| 14 | g.28768305C>G | CA389476380 | FOXG1 | c.1026C>G (p.Ser342Arg) | |
| 14 | g.28768305C>T | CA7140650 | FOXG1 | c.1026C>T (p.Ser342=) | dbSNP ExAC gnomAD v2 |
| 14 | g.28768306T>A | CA389476381 | FOXG1 | c.1027T>A (p.Ser343Thr) | |
| 14 | g.28768306T>C | CA389476382 | FOXG1 | c.1027T>C (p.Ser343Pro) | |
| 14 | g.28768306T>G | CA389476383 | FOXG1 | c.1027T>G (p.Ser343Ala) | |
| 14 | g.28768307C>A | CA389476384 | FOXG1 | c.1028C>A (p.Ser343Tyr) | |
| 14 | g.28768307C= | CA2126000367 | FOXG1 | c.1028C= (p.Ser343=) | |
| 14 | g.28768307C>G | CA389476385 | FOXG1 | c.1028C>G (p.Ser343Cys) | |
| 14 | g.28768307C>T | CA389476386 | FOXG1 | c.1028C>T (p.Ser343Phe) | dbSNP gnomAD v2 |
| 14 | g.28768308C>A | CA486098441 | FOXG1 | c.1029C>A (p.Ser343=) | |
| 14 | g.28768308C>G | CA486098445 | FOXG1 | c.1029C>G (p.Ser343=) | |
| 14 | g.28768308C>T | CA486098443 | FOXG1 | c.1029C>T (p.Ser343=) | ClinVar |
| 14 | g.28768309G>A | CA7140651 | FOXG1 | c.1030G>A (p.Val344Met) | dbSNP ExAC gnomAD v2 |
| 14 | g.28768309G>C | CA389476388 | FOXG1 | c.1030G>C (p.Val344Leu) | |
| 14 | g.28768309G= | CA2126000368 | FOXG1 | c.1030G= (p.Val344=) | |
| 14 | g.28768309G>T | CA389476387 | FOXG1 | c.1030G>T (p.Val344Leu) | |
| 14 | g.28768311_28768312del | CA2695199810 | FOXG1 | c.1032_1033del (p.Leu345AspfsTer?) | ClinVar |
| 14 | g.28768310T>A | CA389476389 | FOXG1 | c.1031T>A (p.Val344Glu) | |
| 14 | g.28768310T>C | CA389476390 | FOXG1 | c.1031T>C (p.Val344Ala) | |
| 14 | g.28768310T>G | CA389476391 | FOXG1 | c.1031T>G (p.Val344Gly) | |
| 14 | g.28768311G>A | CA486098451 | FOXG1 | c.1032G>A (p.Val344=) | |
| 14 | g.28768311G>C | CA486098453 | FOXG1 | c.1032G>C (p.Val344=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28768311G= | CA2126000369 | FOXG1 | c.1032G= (p.Val344=) | |
| 14 | g.28768311G>T | CA7140652 | FOXG1 | c.1032G>T (p.Val344=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.28768312T>A | CA389476392 | FOXG1 | c.1033T>A (p.Leu345Met) | |
| 14 | g.28768312T>C | CA486098454 | FOXG1 | c.1033T>C (p.Leu345=) | |
| 14 | g.28768312T>G | CA389476393 | FOXG1 | c.1033T>G (p.Leu345Val) | |
| 14 | g.28768313T>A | CA389476394 | FOXG1 | c.1034T>A (p.Leu345Ter) | |
| 14 | g.28768313T>C | CA389476395 | FOXG1 | c.1034T>C (p.Leu345Ser) | |
| 14 | g.28768313T>G | CA389476396 | FOXG1 | c.1034T>G (p.Leu345Trp) | |
| 14 | g.28768314G>A | CA486098456 | FOXG1 | c.1035G>A (p.Leu345=) | |
| 14 | g.28768314G>C | CA389476397 | FOXG1 | c.1035G>C (p.Leu345Phe) | |
| 14 | g.28768314G>T | CA389476398 | FOXG1 | c.1035G>T (p.Leu345Phe) | |
| 14 | g.28768315A>C | CA389476400 | FOXG1 | c.1036A>C (p.Thr346Pro) | gnomAD v4 |
| 14 | g.28768315A>G | CA389476401 | FOXG1 | c.1036A>G (p.Thr346Ala) | |
| 14 | g.28768315A>T | CA389476399 | FOXG1 | c.1036A>T (p.Thr346Ser) | |
| 14 | g.28768316del | CA2739277847 | FOXG1 | c.1037del (p.Thr346IlefsTer17) | ClinVar |
| 14 | g.28768316C>A | CA389476402 | FOXG1 | c.1037C>A (p.Thr346Asn) | |
| 14 | g.28768316C>G | CA389476403 | FOXG1 | c.1037C>G (p.Thr346Ser) | |
| 14 | g.28768316C>T | CA389476404 | FOXG1 | c.1037C>T (p.Thr346Ile) | COSMIC |
| 14 | g.28768317T>A | CA486098462 | FOXG1 | c.1038T>A (p.Thr346=) | |
| 14 | g.28768317T>C | CA486098465 | FOXG1 | c.1038T>C (p.Thr346=) | |
| 14 | g.28768317T>G | CA486098467 | FOXG1 | c.1038T>G (p.Thr346=) | |
| 14 | g.28768318C>A | CA389476405 | FOXG1 | c.1039C>A (p.Gln347Lys) | |
| 14 | g.28768318C>G | CA389476406 | FOXG1 | c.1039C>G (p.Gln347Glu) | |
| 14 | g.28768318C>T | CA389476407 | FOXG1 | c.1039C>T (p.Gln347Ter) | |
| 14 | g.28768319A>C | CA389476408 | FOXG1 | c.1040A>C (p.Gln347Pro) | ClinVar gnomAD v4 |
| 14 | g.28768319A>G | CA389476409 | FOXG1 | c.1040A>G (p.Gln347Arg) | |
| 14 | g.28768319A>T | CA389476410 | FOXG1 | c.1040A>T (p.Gln347Leu) | |
| 14 | g.28768320G>A | CA486098470 | FOXG1 | c.1041G>A (p.Gln347=) | gnomAD v4 COSMIC |
| 14 | g.28768320G>C | CA389476411 | FOXG1 | c.1041G>C (p.Gln347His) | |
| 14 | g.28768320G>T | CA389476412 | FOXG1 | c.1041G>T (p.Gln347His) | |
| 14 | g.28768321A>C | CA389476415 | FOXG1 | c.1042A>C (p.Asn348His) | |
| 14 | g.28768321A>G | CA389476414 | FOXG1 | c.1042A>G (p.Asn348Asp) | |
| 14 | g.28768321A>T | CA389476413 | FOXG1 | c.1042A>T (p.Asn348Tyr) | |
| 14 | g.28768322A>C | CA389476416 | FOXG1 | c.1043A>C (p.Asn348Thr) | |
| 14 | g.28768322A>G | CA389476417 | FOXG1 | c.1043A>G (p.Asn348Ser) | ClinVar |
| 14 | g.28768322A>T | CA389476418 | FOXG1 | c.1043A>T (p.Asn348Ile) | |
| 14 | g.28768323C>A | CA389476419 | FOXG1 | c.1044C>A (p.Asn348Lys) | |
| 14 | g.28768323C= | CA2126000370 | FOXG1 | c.1044C= (p.Asn348=) | |
| 14 | g.28768323C>G | CA389476420 | FOXG1 | c.1044C>G (p.Asn348Lys) | |
| 14 | g.28768323C>T | CA486098477 | FOXG1 | c.1044C>T (p.Asn348=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28768324T>A | CA389476421 | FOXG1 | c.1045T>A (p.Ser349Thr) | |
| 14 | g.28768324T>C | CA389476422 | FOXG1 | c.1045T>C (p.Ser349Pro) | |
| 14 | g.28768324T>G | CA314631 | FOXG1 | c.1045T>G (p.Ser349Ala) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28768324T= | CA2126000371 | FOXG1 | c.1045T= (p.Ser349=) | |
| 14 | g.28768325C>A | CA389476423 | FOXG1 | c.1046C>A (p.Ser349Ter) | |
| 14 | g.28768325C>G | CA389476424 | FOXG1 | c.1046C>G (p.Ser349Trp) | |
| 14 | g.28768325C>T | CA389476425 | FOXG1 | c.1046C>T (p.Ser349Leu) | COSMIC |
| 14 | g.28768326G>A | CA486098480 | FOXG1 | c.1047G>A (p.Ser349=) | |
| 14 | g.28768326G>C | CA486098482 | FOXG1 | c.1047G>C (p.Ser349=) | |
| 14 | g.28768326G= | CA2126000372 | FOXG1 | c.1047G= (p.Ser349=) | |
| 14 | g.28768326G>T | CA486098484 | FOXG1 | c.1047G>T (p.Ser349=) | dbSNP gnomAD v4 |
| 14 | g.28768327C>A | CA389476426 | FOXG1 | c.1048C>A (p.Leu350Met) | |
| 14 | g.28768327C= | CA2126000373 | FOXG1 | c.1048C= (p.Leu350=) | |
| 14 | g.28768327C>G | CA389476427 | FOXG1 | c.1048C>G (p.Leu350Val) | gnomAD v4 |
| 14 | g.28768327C>T | CA486098485 | FOXG1 | c.1048C>T (p.Leu350=) | dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 14 | g.28768328T>A | CA389476429 | FOXG1 | c.1049T>A (p.Leu350Gln) | |
| 14 | g.28768328T>C | CA389476430 | FOXG1 | c.1049T>C (p.Leu350Pro) | |
| 14 | g.28768328T>G | CA389476428 | FOXG1 | c.1049T>G (p.Leu350Arg) | |
| 14 | g.28768329G>A | CA486098486 | FOXG1 | c.1050G>A (p.Leu350=) | COSMIC |
| 14 | g.28768329G>C | CA486098488 | FOXG1 | c.1050G>C (p.Leu350=) | |
| 14 | g.28768329G>T | CA486098489 | FOXG1 | c.1050G>T (p.Leu350=) | |
| 14 | g.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.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) |