Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.28768010_28768020delinsGCCACTACGAC | CA2126000099 | FOXG1 | c.731_741delinsGCCACTACGAC (p.Arg244=) | |
14 | g.28768011_28768020del | CA658798196 | FOXG1 | c.732_741del (p.His245ThrfsTer?) | ClinVar dbSNP |
14 | g.28768015T>A | CA389475752 | FOXG1 | c.736T>A (p.Tyr246Asn) | dbSNP |
14 | g.28768015T>C | CA389475753 | FOXG1 | c.736T>C (p.Tyr246His) | |
14 | g.28768015T>G | CA389475754 | FOXG1 | c.736T>G (p.Tyr246Asp) | |
14 | g.28768016A>C | CA389475755 | FOXG1 | c.737A>C (p.Tyr246Ser) | |
14 | g.28768016A>G | CA389475756 | FOXG1 | c.737A>G (p.Tyr246Cys) | |
14 | g.28768016A>T | CA389475757 | FOXG1 | c.737A>T (p.Tyr246Phe) | COSMIC |
14 | g.28768017C>A | CA389475758 | FOXG1 | c.738C>A (p.Tyr246Ter) | |
14 | g.28768017C= | CA2126000122 | FOXG1 | c.738C= (p.Tyr246=) | |
14 | g.28768017C>G | CA389475759 | FOXG1 | c.738C>G (p.Tyr246Ter) | ClinVar dbSNP |
14 | g.28768017C>T | CA486098863 | FOXG1 | c.738C>T (p.Tyr246=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.28768018G>A | CA389475762 | FOXG1 | c.739G>A (p.Asp247Asn) | gnomAD v4 COSMIC |
14 | g.28768018G>C | CA389475761 | FOXG1 | c.739G>C (p.Asp247His) | |
14 | g.28768018G>T | CA389475760 | FOXG1 | c.739G>T (p.Asp247Tyr) | |
14 | g.28768019A>C | CA389475763 | FOXG1 | c.740A>C (p.Asp247Ala) | |
14 | g.28768019A>G | CA389475764 | FOXG1 | c.740A>G (p.Asp247Gly) | |
14 | g.28768019A>T | CA389475765 | FOXG1 | c.740A>T (p.Asp247Val) | |
14 | g.28768020C>A | CA389475766 | FOXG1 | c.741C>A (p.Asp247Glu) | |
14 | g.28768020C>G | CA389475767 | FOXG1 | c.741C>G (p.Asp247Glu) | |
14 | g.28768020C>T | CA486098867 | FOXG1 | c.741C>T (p.Asp247=) | |
14 | g.28768021G>A | CA389475768 | FOXG1 | c.742G>A (p.Asp248Asn) | COSMIC |
14 | g.28768021G>C | CA389475769 | FOXG1 | c.742G>C (p.Asp248His) | gnomAD v4 |
14 | g.28768021G>T | CA389475770 | FOXG1 | c.742G>T (p.Asp248Tyr) | |
14 | g.28768022A>C | CA389475771 | FOXG1 | c.743A>C (p.Asp248Ala) | |
14 | g.28768022A>G | CA389475772 | FOXG1 | c.743A>G (p.Asp248Gly) | |
14 | g.28768022A>T | CA389475773 | FOXG1 | c.743A>T (p.Asp248Val) | |
14 | g.28768023C>A | CA389475774 | FOXG1 | c.744C>A (p.Asp248Glu) | |
14 | g.28768023C>G | CA389475775 | FOXG1 | c.744C>G (p.Asp248Glu) | |
14 | g.28768023C>T | CA486098871 | FOXG1 | c.744C>T (p.Asp248=) | gnomAD v4 |
14 | g.28768024C>A | CA389475777 | FOXG1 | c.745C>A (p.Pro249Thr) | COSMIC |
14 | g.28768024C>G | CA389475778 | FOXG1 | c.745C>G (p.Pro249Ala) | |
14 | g.28768024C>T | CA389475776 | FOXG1 | c.745C>T (p.Pro249Ser) | |
14 | g.28768025C>A | CA389475780 | FOXG1 | c.746C>A (p.Pro249Gln) | |
14 | g.28768025C>G | CA389475779 | FOXG1 | c.746C>G (p.Pro249Arg) | |
14 | g.28768025C>T | CA389475781 | FOXG1 | c.746C>T (p.Pro249Leu) | |
14 | g.28768026G>A | CA486098872 | FOXG1 | c.747G>A (p.Pro249=) | gnomAD v4 |
14 | g.28768026G>C | CA486098874 | FOXG1 | c.747G>C (p.Pro249=) | gnomAD v3 gnomAD v4 |
14 | g.28768026G>T | CA486098875 | FOXG1 | c.747G>T (p.Pro249=) | COSMIC |
14 | g.28768027G>A | CA389475782 | FOXG1 | c.748G>A (p.Gly250Ser) | ClinVar |
14 | g.28768027G>C | CA389475784 | FOXG1 | c.748G>C (p.Gly250Arg) | ClinVar dbSNP |
14 | g.28768027G>T | CA389475783 | FOXG1 | c.748G>T (p.Gly250Cys) | |
14 | g.28768028G>A | CA389475785 | FOXG1 | c.749G>A (p.Gly250Asp) | ClinVar dbSNP |
14 | g.28768028G>C | CA389475786 | FOXG1 | c.749G>C (p.Gly250Ala) | |
14 | g.28768028G= | CA2126000128 | FOXG1 | c.749G= (p.Gly250=) | |
14 | g.28768028G>T | CA389475787 | FOXG1 | c.749G>T (p.Gly250Val) | |
14 | g.28768029C>A | CA486098876 | FOXG1 | c.750C>A (p.Gly250=) | |
14 | g.28768029C= | CA2126000134 | FOXG1 | c.750C= (p.Gly250=) | |
14 | g.28768029C>G | CA486098878 | FOXG1 | c.750C>G (p.Gly250=) | gnomAD v4 |
14 | g.28768029C>T | CA7140628 | FOXG1 | c.750C>T (p.Gly250=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |