| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 14 | g.28767794_28767856del | CA2573053892 | FOXG1 | c.515_577del (p.Gly172_Met192del) | ClinVar dbSNP |
| 14 | g.28767833G>A | CA389475348 | FOXG1 | c.554G>A (p.Ser185Asn) | |
| 14 | g.28767833G>C | CA389475349 | FOXG1 | c.554G>C (p.Ser185Thr) | ClinVar dbSNP |
| 14 | g.28767833G= | CA2125999756 | FOXG1 | c.554G= (p.Ser185=) | |
| 14 | g.28767833G>T | CA10654909 | FOXG1 | c.554G>T (p.Ser185Ile) | ClinVar dbSNP |
| 14 | g.28767834C>A | CA389475351 | FOXG1 | c.555C>A (p.Ser185Arg) | |
| 14 | g.28767834C= | CA2125999760 | FOXG1 | c.555C= (p.Ser185=) | |
| 14 | g.28767834C>G | CA389475350 | FOXG1 | c.555C>G (p.Ser185Arg) | |
| 14 | g.28767834C>T | CA7140617 | FOXG1 | c.555C>T (p.Ser185=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28767835T>A | CA389475352 | FOXG1 | c.556T>A (p.Tyr186Asn) | |
| 14 | g.28767835T>C | CA389475353 | FOXG1 | c.556T>C (p.Tyr186His) | |
| 14 | g.28767835T>G | CA389475354 | FOXG1 | c.556T>G (p.Tyr186Asp) | |
| 14 | g.28767836A>C | CA389475355 | FOXG1 | c.557A>C (p.Tyr186Ser) | |
| 14 | g.28767836A>G | CA389475356 | FOXG1 | c.557A>G (p.Tyr186Cys) | |
| 14 | g.28767836A>T | CA389475357 | FOXG1 | c.557A>T (p.Tyr186Phe) | |
| 14 | g.28767838_28767840del | CA2580088007 | FOXG1 | c.559_561del (p.Asn187del) | ClinVar |
| 14 | g.28767837C>A | CA389475358 | FOXG1 | c.558C>A (p.Tyr186Ter) | |
| 14 | g.28767837C>G | CA389475359 | FOXG1 | c.558C>G (p.Tyr186Ter) | |
| 14 | g.28767837C>T | CA486098549 | FOXG1 | c.558C>T (p.Tyr186=) | |
| 14 | g.28767838A>C | CA389475360 | FOXG1 | c.559A>C (p.Asn187His) | |
| 14 | g.28767838A>G | CA389475361 | FOXG1 | c.559A>G (p.Asn187Asp) | ClinVar dbSNP |
| 14 | g.28767838A>T | CA389475362 | FOXG1 | c.559A>T (p.Asn187Tyr) | ClinVar dbSNP |
| 14 | g.28767839A>C | CA389475363 | FOXG1 | c.560A>C (p.Asn187Thr) | |
| 14 | g.28767839A>G | CA389475364 | FOXG1 | c.560A>G (p.Asn187Ser) | |
| 14 | g.28767839A>T | CA389475365 | FOXG1 | c.560A>T (p.Asn187Ile) | |
| 14 | g.28767840C>A | CA204685 | FOXG1 | c.561C>A (p.Asn187Lys) | ClinVar dbSNP |
| 14 | g.28767840C= | CA2125999767 | FOXG1 | c.561C= (p.Asn187=) | |
| 14 | g.28767840C>G | CA10588574 | FOXG1 | c.561C>G (p.Asn187Lys) | ClinVar dbSNP |
| 14 | g.28767840C>T | CA486098554 | FOXG1 | c.561C>T (p.Asn187=) | COSMIC |
| 14 | g.28767841G>A | CA389475366 | FOXG1 | c.562G>A (p.Ala188Thr) | COSMIC |
| 14 | g.28767841G>C | CA389475367 | FOXG1 | c.562G>C (p.Ala188Pro) | |
| 14 | g.28767841G>T | CA389475368 | FOXG1 | c.562G>T (p.Ala188Ser) | |
| 14 | g.28767842C>A | CA389475369 | FOXG1 | c.563C>A (p.Ala188Glu) | ClinVar dbSNP |
| 14 | g.28767842C= | CA2125999773 | FOXG1 | c.563C= (p.Ala188=) | |
| 14 | g.28767842C>G | CA172187 | FOXG1 | c.563C>G (p.Ala188Gly) | ClinVar dbSNP |
| 14 | g.28767842C>T | CA389475370 | FOXG1 | c.563C>T (p.Ala188Val) | COSMIC |
| 14 | g.28767843G>A | CA486098560 | FOXG1 | c.564G>A (p.Ala188=) | ClinVar dbSNP gnomAD v4 |
| 14 | g.28767843G>C | CA486098561 | FOXG1 | c.564G>C (p.Ala188=) | gnomAD v4 |
| 14 | g.28767843G>T | CA486098562 | FOXG1 | c.564G>T (p.Ala188=) | |
| 14 | g.28767844C>A | CA389475371 | FOXG1 | c.565C>A (p.Leu189Ile) | |
| 14 | g.28767844C= | CA2125999778 | FOXG1 | c.565C= (p.Leu189=) | |
| 14 | g.28767844C>G | CA389475372 | FOXG1 | c.565C>G (p.Leu189Val) | ClinVar dbSNP |
| 14 | g.28767844C>T | CA389475373 | FOXG1 | c.565C>T (p.Leu189Phe) | ClinVar dbSNP |
| 14 | g.28767845T>A | CA389475374 | FOXG1 | c.566T>A (p.Leu189His) | |
| 14 | g.28767845T>C | CA389475375 | FOXG1 | c.566T>C (p.Leu189Pro) | |
| 14 | g.28767845T>G | CA389475376 | FOXG1 | c.566T>G (p.Leu189Arg) | |
| 14 | g.28767846C>A | CA486098572 | FOXG1 | c.567C>A (p.Leu189=) | |
| 14 | g.28767846C= | CA2125999781 | FOXG1 | c.567C= (p.Leu189=) | |
| 14 | g.28767846C>G | CA486098573 | FOXG1 | c.567C>G (p.Leu189=) | |
| 14 | g.28767846C>T | CA7140618 | FOXG1 | c.567C>T (p.Leu189=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |