Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.28767794_28767856del | CA2573053892 | FOXG1 | c.515_577del (p.Gly172_Met192del) | ClinVar dbSNP |
14 | g.28767824C>A | CA389475330 | FOXG1 | c.545C>A (p.Pro182Gln) | ClinVar dbSNP |
14 | g.28767824C= | CA2125999727 | FOXG1 | c.545C= (p.Pro182=) | |
14 | g.28767824C>G | CA389475331 | FOXG1 | c.545C>G (p.Pro182Arg) | |
14 | g.28767824C>T | CA314608 | FOXG1 | c.545C>T (p.Pro182Leu) | ClinVar dbSNP |
14 | g.28767825G>A | CA7140615 | FOXG1 | c.546G>A (p.Pro182=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
14 | g.28767825G>C | CA486098520 | FOXG1 | c.546G>C (p.Pro182=) | ClinVar gnomAD v4 |
14 | g.28767825G= | CA2125999730 | FOXG1 | c.546G= (p.Pro182=) | |
14 | g.28767825G>T | CA486098522 | FOXG1 | c.546G>T (p.Pro182=) | |
14 | g.28767826C>A | CA389475332 | FOXG1 | c.547C>A (p.Pro183Thr) | |
14 | g.28767826C>G | CA389475333 | FOXG1 | c.547C>G (p.Pro183Ala) | |
14 | g.28767826C>T | CA389475334 | FOXG1 | c.547C>T (p.Pro183Ser) | |
14 | g.28767827C>A | CA389475335 | FOXG1 | c.548C>A (p.Pro183Gln) | |
14 | g.28767827C= | CA2125999732 | FOXG1 | c.548C= (p.Pro183=) | |
14 | g.28767827C>G | CA389475336 | FOXG1 | c.548C>G (p.Pro183Arg) | dbSNP |
14 | g.28767827C>T | CA389475337 | FOXG1 | c.548C>T (p.Pro183Leu) | COSMIC |
14 | g.28767828G>A | CA7140616 | FOXG1 | c.549G>A (p.Pro183=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
14 | g.28767828G>C | CA486098530 | FOXG1 | c.549G>C (p.Pro183=) | |
14 | g.28767828G= | CA2125999734 | FOXG1 | c.549G= (p.Pro183=) | |
14 | g.28767828G>T | CA486098528 | FOXG1 | c.549G>T (p.Pro183=) | gnomAD v4 |
14 | g.28767829T>A | CA389475340 | FOXG1 | c.550T>A (p.Phe184Ile) | |
14 | g.28767829T>C | CA389475339 | FOXG1 | c.550T>C (p.Phe184Leu) | dbSNP |
14 | g.28767829T>G | CA389475338 | FOXG1 | c.550T>G (p.Phe184Val) | |
14 | g.28767829T= | CA2125999736 | FOXG1 | c.550T= (p.Phe184=) | |
14 | g.28767830T>A | CA389475341 | FOXG1 | c.551T>A (p.Phe184Tyr) | |
14 | g.28767830T>C | CA389475342 | FOXG1 | c.551T>C (p.Phe184Ser) | |
14 | g.28767830T>G | CA389475343 | FOXG1 | c.551T>G (p.Phe184Cys) | |
14 | g.28767830T= | CA2125999738 | FOXG1 | c.551T= (p.Phe184=) | |
14 | g.28767830_28767831delinsTC | CA2125999740 | FOXG1 | c.551_552delinsTC (p.Phe184=) | |
14 | g.28767831del | CA915948875 | FOXG1 | c.552del (p.Phe184LeufsTer8) | ClinVar dbSNP |
14 | g.28767831C>A | CA389475344 | FOXG1 | c.552C>A (p.Phe184Leu) | |
14 | g.28767831C>G | CA389475345 | FOXG1 | c.552C>G (p.Phe184Leu) | COSMIC |
14 | g.28767831C>T | CA486098541 | FOXG1 | c.552C>T (p.Phe184=) | gnomAD v4 |
14 | g.28767831dup | CA199437 | FOXG1 | c.552dup (p.Ser185GlnfsTer?) | ClinVar dbSNP |
14 | g.28767832A= | CA2125999753 | FOXG1 | c.553A= (p.Ser185=) | |
14 | g.28767832A>C | CA389475346 | FOXG1 | c.553A>C (p.Ser185Arg) | |
14 | g.28767832A>G | CA389475347 | FOXG1 | c.553A>G (p.Ser185Gly) | ClinVar dbSNP |
14 | g.28767832A>T | CA10586143 | FOXG1 | c.553A>T (p.Ser185Cys) | 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) |