| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 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=) |