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.28768004_28768010dup | CA2580088018 | FOXG1 | c.725_731dup (p.His245AlafsTer?) | ClinVar |
| 14 | g.28768010G>A | CA16619864 | FOXG1 | c.731G>A (p.Arg244His) | ClinVar dbSNP |
| 14 | g.28768010G>C | CA389475743 | FOXG1 | c.731G>C (p.Arg244Pro) | |
| 14 | g.28768010G= | CA2126000094 | FOXG1 | c.731G= (p.Arg244=) | |
| 14 | g.28768010G>T | CA314654 | FOXG1 | c.731G>T (p.Arg244Leu) | dbSNP |
| 14 | g.28768010_28768020delinsGCCACTACGAC | CA2126000099 | FOXG1 | c.731_741delinsGCCACTACGAC (p.Arg244=) | |
| 14 | g.28768011C>A | CA486098855 | FOXG1 | c.732C>A (p.Arg244=) | COSMIC |
| 14 | g.28768011C>G | CA486098856 | FOXG1 | c.732C>G (p.Arg244=) | gnomAD v3 gnomAD v4 |
| 14 | g.28768011C>T | CA486098857 | FOXG1 | c.732C>T (p.Arg244=) | |
| 14 | g.28768011_28768020del | CA658798196 | FOXG1 | c.732_741del (p.His245ThrfsTer?) | ClinVar dbSNP |
| 14 | g.28768012C>A | CA389475745 | FOXG1 | c.733C>A (p.His245Asn) | COSMIC |
| 14 | g.28768012C>G | CA389475746 | FOXG1 | c.733C>G (p.His245Asp) | |
| 14 | g.28768012C>T | CA389475744 | FOXG1 | c.733C>T (p.His245Tyr) | COSMIC |
| 14 | g.28768013A>C | CA389475747 | FOXG1 | c.734A>C (p.His245Pro) | |
| 14 | g.28768013A>G | CA389475748 | FOXG1 | c.734A>G (p.His245Arg) | COSMIC |
| 14 | g.28768013A>T | CA389475749 | FOXG1 | c.734A>T (p.His245Leu) | |
| 14 | g.28768014del | CA2573053897 | FOXG1 | c.735del (p.Tyr246ThrfsTer?) | ClinVar dbSNP |
| 14 | g.28768014C>A | CA389475750 | FOXG1 | c.735C>A (p.His245Gln) | |
| 14 | g.28768014C= | CA2126000113 | FOXG1 | c.735C= (p.His245=) | |
| 14 | g.28768014C>G | CA389475751 | FOXG1 | c.735C>G (p.His245Gln) | |
| 14 | g.28768014C>T | CA486098861 | FOXG1 | c.735C>T (p.His245=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 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 |
| 14 | g.28768030A>C | CA389475788 | FOXG1 | c.751A>C (p.Lys251Gln) | |
| 14 | g.28768030A>G | CA389475789 | FOXG1 | c.751A>G (p.Lys251Glu) | |
| 14 | g.28768030A>T | CA389475790 | FOXG1 | c.751A>T (p.Lys251Ter) | |
| 14 | g.28768031A>C | CA389475791 | FOXG1 | c.752A>C (p.Lys251Thr) | |
| 14 | g.28768031A>G | CA389475792 | FOXG1 | c.752A>G (p.Lys251Arg) | |
| 14 | g.28768031A>T | CA389475793 | FOXG1 | c.752A>T (p.Lys251Met) | |
| 14 | g.28768032G>A | CA486098880 | FOXG1 | c.753G>A (p.Lys251=) | ClinVar dbSNP gnomAD v4 |
| 14 | g.28768032G>C | CA389475794 | FOXG1 | c.753G>C (p.Lys251Asn) | |
| 14 | g.28768032G>T | CA389475795 | FOXG1 | c.753G>T (p.Lys251Asn) | |
| 14 | g.28768034dup | CA2695219195 | FOXG1 | c.755dup (p.Asn253GlnfsTer?) | |
| 14 | g.28768033G>A | CA389475796 | FOXG1 | c.754G>A (p.Gly252Ser) | |
| 14 | g.28768033G>C | CA389475798 | FOXG1 | c.754G>C (p.Gly252Arg) | |
| 14 | g.28768033G>T | CA389475797 | FOXG1 | c.754G>T (p.Gly252Cys) | |
| 14 | g.28768034G>A | CA389475799 | FOXG1 | c.755G>A (p.Gly252Asp) | ClinVar dbSNP |
| 14 | g.28768034G>C | CA389475800 | FOXG1 | c.755G>C (p.Gly252Ala) | |
| 14 | g.28768034G= | CA2126000140 | FOXG1 | c.755G= (p.Gly252=) | |
| 14 | g.28768034G>T | CA172191 | FOXG1 | c.755G>T (p.Gly252Val) | ClinVar dbSNP |
| 14 | g.28768035C>A | CA486098887 | FOXG1 | c.756C>A (p.Gly252=) | |
| 14 | g.28768035C= | CA2126000143 | FOXG1 | c.756C= (p.Gly252=) | |
| 14 | g.28768035C>G | CA486098883 | FOXG1 | c.756C>G (p.Gly252=) | gnomAD v4 |
| 14 | g.28768035C>T | CA486098885 | FOXG1 | c.756C>T (p.Gly252=) | dbSNP gnomAD v4 |
| 14 | g.28768036A= | CA2126000152 | FOXG1 | c.757A= (p.Asn253=) | |
| 14 | g.28768036A>C | CA389475801 | FOXG1 | c.757A>C (p.Asn253His) | |
| 14 | g.28768036A>G | CA172193 | FOXG1 | c.757A>G (p.Asn253Asp) | ClinVar dbSNP |
| 14 | g.28768036A>T | CA389475802 | FOXG1 | c.757A>T (p.Asn253Tyr) | |
| 14 | g.28768037_28768040dup | CA915948877 | FOXG1 | c.758_761dup (p.Tyr254Ter) | ClinVar dbSNP |
| 14 | g.28768037A>C | CA389475803 | FOXG1 | c.758A>C (p.Asn253Thr) | |
| 14 | g.28768037A>G | CA389475804 | FOXG1 | c.758A>G (p.Asn253Ser) | gnomAD v4 |
| 14 | g.28768037A>T | CA389475805 | FOXG1 | c.758A>T (p.Asn253Ile) | |
| 14 | g.28768038C>A | CA389475806 | FOXG1 | c.759C>A (p.Asn253Lys) | ClinVar dbSNP |
| 14 | g.28768038C= | CA2126000165 | FOXG1 | c.759C= (p.Asn253=) | |
| 14 | g.28768038C>G | CA389475807 | FOXG1 | c.759C>G (p.Asn253Lys) | |
| 14 | g.28768038C>T | CA7140629 | FOXG1 | c.759C>T (p.Asn253=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.28768039T>A | CA389475808 | FOXG1 | c.760T>A (p.Tyr254Asn) | |
| 14 | g.28768039T>C | CA389475809 | FOXG1 | c.760T>C (p.Tyr254His) | |
| 14 | g.28768039T>G | CA389475810 | FOXG1 | c.760T>G (p.Tyr254Asp) | |
| 14 | g.28768040A= | CA2126000169 | FOXG1 | c.761A= (p.Tyr254=) | |
| 14 | g.28768040A>C | CA389475811 | FOXG1 | c.761A>C (p.Tyr254Ser) | |
| 14 | g.28768040A>G | CA389475812 | FOXG1 | c.761A>G (p.Tyr254Cys) | ClinVar dbSNP |
| 14 | g.28768040A>T | CA389475813 | FOXG1 | c.761A>T (p.Tyr254Phe) | |
| 14 | g.28768041C>A | CA389475814 | FOXG1 | c.762C>A (p.Tyr254Ter) | ClinVar dbSNP |
| 14 | g.28768041C= | CA2126000174 | FOXG1 | c.762C= (p.Tyr254=) | |
| 14 | g.28768041C>G | CA172195 | FOXG1 | c.762C>G (p.Tyr254Ter) | ClinVar dbSNP |
| 14 | g.28768041C>T | CA486098892 | FOXG1 | c.762C>T (p.Tyr254=) | |
| 14 | g.28768042T>A | CA389475815 | FOXG1 | c.763T>A (p.Trp255Arg) | ClinVar |
| 14 | g.28768042T>C | CA389475816 | FOXG1 | c.763T>C (p.Trp255Arg) | ClinVar |
| 14 | g.28768042T>G | CA389475817 | FOXG1 | c.763T>G (p.Trp255Gly) | |
| 14 | g.28768043G>A | CA389475819 | FOXG1 | c.764G>A (p.Trp255Ter) | ClinVar dbSNP COSMIC |
| 14 | g.28768043G>C | CA389475820 | FOXG1 | c.764G>C (p.Trp255Ser) | |
| 14 | g.28768043G= | CA2126000181 | FOXG1 | c.764G= (p.Trp255=) | |
| 14 | g.28768043G>T | CA389475818 | FOXG1 | c.764G>T (p.Trp255Leu) | |
| 14 | g.28768044G>A | CA123550 | FOXG1 | c.765G>A (p.Trp255Ter) | ClinVar dbSNP |
| 14 | g.28768044G>C | CA389475821 | FOXG1 | c.765G>C (p.Trp255Cys) | ClinVar |
| 14 | g.28768044G= | CA2126000188 | FOXG1 | c.765G= (p.Trp255=) | |
| 14 | g.28768044G>T | CA172197 | FOXG1 | c.765G>T (p.Trp255Cys) | ClinVar dbSNP |
| 14 | g.28768045A>C | CA389475822 | FOXG1 | c.766A>C (p.Met256Leu) | |
| 14 | g.28768045A>G | CA389475823 | FOXG1 | c.766A>G (p.Met256Val) | |
| 14 | g.28768045A>T | CA389475824 | FOXG1 | c.766A>T (p.Met256Leu) | |
| 14 | g.28768046T>A | CA389475825 | FOXG1 | c.767T>A (p.Met256Lys) | COSMIC |
| 14 | g.28768046T>C | CA389475827 | FOXG1 | c.767T>C (p.Met256Thr) | |
| 14 | g.28768046T>G | CA389475826 | FOXG1 | c.767T>G (p.Met256Arg) | |
| 14 | g.28768047G>A | CA389475828 | FOXG1 | c.768G>A (p.Met256Ile) | |
| 14 | g.28768047G>C | CA389475829 | FOXG1 | c.768G>C (p.Met256Ile) | gnomAD v4 |
| 14 | g.28768047G>T | CA389475830 | FOXG1 | c.768G>T (p.Met256Ile) | dbSNP |
| 14 | g.28768048C>A | CA389475831 | FOXG1 | c.769C>A (p.Leu257Met) | |
| 14 | g.28768048C>G | CA389475832 | FOXG1 | c.769C>G (p.Leu257Val) | |
| 14 | g.28768048C>T | CA486098901 | FOXG1 | c.769C>T (p.Leu257=) | gnomAD v4 |
| 14 | g.28768049T>A | CA389475834 | FOXG1 | c.770T>A (p.Leu257Gln) | |
| 14 | g.28768049T>C | CA389475835 | FOXG1 | c.770T>C (p.Leu257Pro) | ClinVar dbSNP |
| 14 | g.28768049T>G | CA389475833 | FOXG1 | c.770T>G (p.Leu257Arg) | |
| 14 | g.28768049T= | CA2126000194 | FOXG1 | c.770T= (p.Leu257=) | |
| 14 | g.28768050G>A | CA486098902 | FOXG1 | c.771G>A (p.Leu257=) | |
| 14 | g.28768050G>C | CA486098903 | FOXG1 | c.771G>C (p.Leu257=) | gnomAD v4 COSMIC |
| 14 | g.28768050G>T | CA486098904 | FOXG1 | c.771G>T (p.Leu257=) | |
| 14 | g.28768051G>A | CA389475838 | FOXG1 | c.772G>A (p.Asp258Asn) | |
| 14 | g.28768051G>C | CA389475836 | FOXG1 | c.772G>C (p.Asp258His) | |
| 14 | g.28768051G>T | CA389475837 | FOXG1 | c.772G>T (p.Asp258Tyr) | ClinVar dbSNP |
| 14 | g.28768052A>C | CA389475839 | FOXG1 | c.773A>C (p.Asp258Ala) | |
| 14 | g.28768052A>G | CA389475840 | FOXG1 | c.773A>G (p.Asp258Gly) | |
| 14 | g.28768052A>T | CA389475841 | FOXG1 | c.773A>T (p.Asp258Val) | |
| 14 | g.28768053C>A | CA389475842 | FOXG1 | c.774C>A (p.Asp258Glu) | |
| 14 | g.28768053C>G | CA389475843 | FOXG1 | c.774C>G (p.Asp258Glu) | |
| 14 | g.28768053C>T | CA486098906 | FOXG1 | c.774C>T (p.Asp258=) | |
| 14 | g.28768054C>A | CA389475844 | FOXG1 | c.775C>A (p.Pro259Thr) | |
| 14 | g.28768054C>G | CA389475845 | FOXG1 | c.775C>G (p.Pro259Ala) | |
| 14 | g.28768054C>T | CA389475846 | FOXG1 | c.775C>T (p.Pro259Ser) | gnomAD v4 |
| 14 | g.28768055C>A | CA389475847 | FOXG1 | c.776C>A (p.Pro259Gln) | |
| 14 | g.28768055C= | CA2126000201 | FOXG1 | c.776C= (p.Pro259=) | |
| 14 | g.28768055C>G | CA358177 | FOXG1 | c.776C>G (p.Pro259Arg) | ClinVar dbSNP |
| 14 | g.28768055C>T | CA389475848 | FOXG1 | c.776C>T (p.Pro259Leu) | |
| 14 | g.28768055_28768056delinsCG | CA2126000205 | FOXG1 | c.776_777delinsCG (p.Pro259=) | |
| 14 | g.28768056del | CA915948878 | FOXG1 | c.777del (p.Ser260ArgfsTer?) | ClinVar dbSNP |
| 14 | g.28768056G>A | CA486098910 | FOXG1 | c.777G>A (p.Pro259=) | gnomAD v4 |
| 14 | g.28768056G>C | CA486098911 | FOXG1 | c.777G>C (p.Pro259=) | dbSNP |
| 14 | g.28768056G= | CA2126000211 | FOXG1 | c.777G= (p.Pro259=) | |
| 14 | g.28768056G>T | CA486098912 | FOXG1 | c.777G>T (p.Pro259=) | ClinVar dbSNP gnomAD v4 |
| 14 | g.28768057T>A | CA389475851 | FOXG1 | c.778T>A (p.Ser260Thr) | |
| 14 | g.28768057T>C | CA389475849 | FOXG1 | c.778T>C (p.Ser260Pro) | dbSNP |
| 14 | g.28768057T>G | CA389475850 | FOXG1 | c.778T>G (p.Ser260Ala) | |
| 14 | g.28768058C>A | CA389475852 | FOXG1 | c.779C>A (p.Ser260Ter) | |
| 14 | g.28768058C>G | CA389475853 | FOXG1 | c.779C>G (p.Ser260Trp) | |
| 14 | g.28768058C>T | CA389475854 | FOXG1 | c.779C>T (p.Ser260Leu) | |
| 14 | g.28768059G>A | CA486098915 | FOXG1 | c.780G>A (p.Ser260=) | COSMIC |
| 14 | g.28768059G>C | CA486098917 | FOXG1 | c.780G>C (p.Ser260=) | dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.28768059G= | CA2126000213 | FOXG1 | c.780G= (p.Ser260=) | |
| 14 | g.28768059G>T | CA486098918 | FOXG1 | c.780G>T (p.Ser260=) | dbSNP |
| 14 | g.28768060A>C | CA389475855 | FOXG1 | c.781A>C (p.Ser261Arg) | dbSNP |
| 14 | g.28768060A>G | CA389475856 | FOXG1 | c.781A>G (p.Ser261Gly) | |
| 14 | g.28768060A>T | CA389475857 | FOXG1 | c.781A>T (p.Ser261Cys) | |
| 14 | g.28768061G>A | CA389475858 | FOXG1 | c.782G>A (p.Ser261Asn) | dbSNP |
| 14 | g.28768061G>C | CA389475859 | FOXG1 | c.782G>C (p.Ser261Thr) | |
| 14 | g.28768061G>T | CA389475860 | FOXG1 | c.782G>T (p.Ser261Ile) | |
| 14 | g.28768062C>A | CA389475861 | FOXG1 | c.783C>A (p.Ser261Arg) | gnomAD v4 |
| 14 | g.28768062C= | CA2126000219 | FOXG1 | c.783C= (p.Ser261=) | |
| 14 | g.28768062C>G | CA389475862 | FOXG1 | c.783C>G (p.Ser261Arg) | |
| 14 | g.28768062C>T | CA258396579 | FOXG1 | c.783C>T (p.Ser261=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28768063G>A | CA389475865 | FOXG1 | c.784G>A (p.Asp262Asn) | COSMIC |
| 14 | g.28768063G>C | CA389475864 | FOXG1 | c.784G>C (p.Asp262His) | |
| 14 | g.28768063G>T | CA389475863 | FOXG1 | c.784G>T (p.Asp262Tyr) | |
| 14 | g.28768064A>C | CA389475866 | FOXG1 | c.785A>C (p.Asp262Ala) | |
| 14 | g.28768064A>G | CA389475867 | FOXG1 | c.785A>G (p.Asp262Gly) | |
| 14 | g.28768064A>T | CA389475868 | FOXG1 | c.785A>T (p.Asp262Val) | |
| 14 | g.28768065C>A | CA389475869 | FOXG1 | c.786C>A (p.Asp262Glu) | |
| 14 | g.28768065C>G | CA389475870 | FOXG1 | c.786C>G (p.Asp262Glu) | dbSNP |
| 14 | g.28768065C>T | CA486098925 | FOXG1 | c.786C>T (p.Asp262=) | |
| 14 | g.28768065_28768070delinsCGACGT | CA2126000221 | FOXG1 | c.786_791delinsCGACGT (p.Asp262=) | |
| 14 | g.28768066G>A | CA389475873 | FOXG1 | c.787G>A (p.Asp263Asn) | |
| 14 | g.28768066G>C | CA389475872 | FOXG1 | c.787G>C (p.Asp263His) | |
| 14 | g.28768066G>T | CA389475871 | FOXG1 | c.787G>T (p.Asp263Tyr) | |
| 14 | g.28768067_28768071del | CA199445 | FOXG1 | c.788_792del (p.Asp263ValfsTer?) | ClinVar dbSNP |
| 14 | g.28768067A>C | CA389475874 | FOXG1 | c.788A>C (p.Asp263Ala) | |
| 14 | g.28768067A>G | CA389475875 | FOXG1 | c.788A>G (p.Asp263Gly) | COSMIC |
| 14 | g.28768067A>T | CA389475876 | FOXG1 | c.788A>T (p.Asp263Val) | |
| 14 | g.28768068C>A | CA389475877 | FOXG1 | c.789C>A (p.Asp263Glu) | |
| 14 | g.28768068C= | CA2126000231 | FOXG1 | c.789C= (p.Asp263=) | |
| 14 | g.28768068C>G | CA389475878 | FOXG1 | c.789C>G (p.Asp263Glu) | gnomAD v4 |
| 14 | g.28768068C>T | CA258396580 | FOXG1 | c.789C>T (p.Asp263=) | dbSNP |
| 14 | g.28768069G>A | CA389475879 | FOXG1 | c.790G>A (p.Val264Met) | gnomAD v4 |
| 14 | g.28768069G>C | CA389475881 | FOXG1 | c.790G>C (p.Val264Leu) | |
| 14 | g.28768069G>T | CA389475880 | FOXG1 | c.790G>T (p.Val264Leu) | |
| 14 | g.28768070T>A | CA389475882 | FOXG1 | c.791T>A (p.Val264Glu) | |
| 14 | g.28768070T>C | CA389475883 | FOXG1 | c.791T>C (p.Val264Ala) | ClinVar dbSNP |
| 14 | g.28768070T>G | CA389475884 | FOXG1 | c.791T>G (p.Val264Gly) | ClinVar |
| 14 | g.28768070T= | CA2126000237 | FOXG1 | c.791T= (p.Val264=) | |
| 14 | g.28768071G>A | CA486098931 | FOXG1 | c.792G>A (p.Val264=) | gnomAD v4 |
| 14 | g.28768071G>C | CA486098933 | FOXG1 | c.792G>C (p.Val264=) | |
| 14 | g.28768071G>T | CA486098935 | FOXG1 | c.792G>T (p.Val264=) | |
| 14 | g.28768072T>A | CA389475885 | FOXG1 | c.793T>A (p.Phe265Ile) | |
| 14 | g.28768072T>C | CA389475886 | FOXG1 | c.793T>C (p.Phe265Leu) | |
| 14 | g.28768072T>G | CA389475887 | FOXG1 | c.793T>G (p.Phe265Val) | |
| 14 | g.28768072_28768087del | CA2573149903 | FOXG1 | c.793_808del (p.Phe265ArgfsTer?) | ClinVar dbSNP |
| 14 | g.28768073T>A | CA389475888 | FOXG1 | c.794T>A (p.Phe265Tyr) | |
| 14 | g.28768073T>C | CA389475889 | FOXG1 | c.794T>C (p.Phe265Ser) | |
| 14 | g.28768073T>G | CA389475890 | FOXG1 | c.794T>G (p.Phe265Cys) | |
| 14 | g.28768074C>A | CA389475891 | FOXG1 | c.795C>A (p.Phe265Leu) | COSMIC |
| 14 | g.28768074C= | CA2126000248 | FOXG1 | c.795C= (p.Phe265=) | |
| 14 | g.28768074C>G | CA389475892 | FOXG1 | c.795C>G (p.Phe265Leu) | |
| 14 | g.28768074C>T | CA486098942 | FOXG1 | c.795C>T (p.Phe265=) | dbSNP |
| 14 | g.28768075A>C | CA389475895 | FOXG1 | c.796A>C (p.Ile266Leu) | |
| 14 | g.28768075A>G | CA389475894 | FOXG1 | c.796A>G (p.Ile266Val) | gnomAD v4 |
| 14 | g.28768075A>T | CA389475893 | FOXG1 | c.796A>T (p.Ile266Phe) | |
| 14 | g.28768076T>A | CA10603236 | FOXG1 | c.797T>A (p.Ile266Asn) | ClinVar dbSNP |
| 14 | g.28768076T>C | CA389475897 | FOXG1 | c.797T>C (p.Ile266Thr) | ClinVar |
| 14 | g.28768076T>G | CA389475896 | FOXG1 | c.797T>G (p.Ile266Ser) | ClinVar dbSNP |
| 14 | g.28768076T= | CA2126000254 | FOXG1 | c.797T= (p.Ile266=) | |
| 14 | g.28768077C>A | CA486098943 | FOXG1 | c.798C>A (p.Ile266=) | |
| 14 | g.28768077C= | CA2126000262 | FOXG1 | c.798C= (p.Ile266=) | |
| 14 | g.28768077C>G | CA389475898 | FOXG1 | c.798C>G (p.Ile266Met) | |
| 14 | g.28768077C>T | CA7140630 | FOXG1 | c.798C>T (p.Ile266=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.28768081_28768083del | CA2739277845 | FOXG1 | c.802_804del (p.Gly268del) | ClinVar |
| 14 | g.28768078G>A | CA172199 | FOXG1 | c.799G>A (p.Gly267Ser) | ClinVar dbSNP |
| 14 | g.28768078G>C | CA389475899 | FOXG1 | c.799G>C (p.Gly267Arg) | |
| 14 | g.28768078G= | CA2126000267 | FOXG1 | c.799G= (p.Gly267=) | |
| 14 | g.28768078G>T | CA389475900 | FOXG1 | c.799G>T (p.Gly267Cys) | |
| 14 | g.28768079G>A | CA389475901 | FOXG1 | c.800G>A (p.Gly267Asp) | ClinVar |
| 14 | g.28768079G>C | CA389475902 | FOXG1 | c.800G>C (p.Gly267Ala) | |
| 14 | g.28768079G>T | CA389475903 | FOXG1 | c.800G>T (p.Gly267Val) | |
| 14 | g.28768080C>A | CA486098949 | FOXG1 | c.801C>A (p.Gly267=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.28768080C= | CA2126000272 | FOXG1 | c.801C= (p.Gly267=) | |
| 14 | g.28768080C>G | CA486098950 | FOXG1 | c.801C>G (p.Gly267=) | |
| 14 | g.28768080C>T | CA486098951 | FOXG1 | c.801C>T (p.Gly267=) | |
| 14 | g.28768081G>A | CA389475904 | FOXG1 | c.802G>A (p.Gly268Ser) | COSMIC |
| 14 | g.28768081G>C | CA389475905 | FOXG1 | c.802G>C (p.Gly268Arg) | COSMIC |
| 14 | g.28768081G>T | CA389475906 | FOXG1 | c.802G>T (p.Gly268Cys) | |
| 14 | g.28768082del | CA2586963983 | FOXG1 | c.803del (p.Gly268AlafsTer?) | ClinVar |
| 14 | g.28768082G>A | CA389475907 | FOXG1 | c.803G>A (p.Gly268Asp) | |
| 14 | g.28768082G>C | CA389475908 | FOXG1 | c.803G>C (p.Gly268Ala) | |
| 14 | g.28768082G>T | CA389475909 | FOXG1 | c.803G>T (p.Gly268Val) | ClinVar dbSNP gnomAD v4 |
| 14 | g.28768083C>A | CA486098955 | FOXG1 | c.804C>A (p.Gly268=) | gnomAD v4 |
| 14 | g.28768083C>G | CA486098957 | FOXG1 | c.804C>G (p.Gly268=) | |
| 14 | g.28768083C>T | CA486098956 | FOXG1 | c.804C>T (p.Gly268=) | ClinVar |
| 14 | g.28768084A>C | CA389475912 | FOXG1 | c.805A>C (p.Thr269Pro) | gnomAD v4 |
| 14 | g.28768084A>G | CA389475910 | FOXG1 | c.805A>G (p.Thr269Ala) | |
| 14 | g.28768084A>T | CA389475911 | FOXG1 | c.805A>T (p.Thr269Ser) | |
| 14 | g.28768085C>A | CA389475913 | FOXG1 | c.806C>A (p.Thr269Asn) | |
| 14 | g.28768085C>G | CA389475914 | FOXG1 | c.806C>G (p.Thr269Ser) | |
| 14 | g.28768085C>T | CA389475915 | FOXG1 | c.806C>T (p.Thr269Ile) | |
| 14 | g.28768086C>A | CA486098967 | FOXG1 | c.807C>A (p.Thr269=) | |
| 14 | g.28768086C>G | CA486098968 | FOXG1 | c.807C>G (p.Thr269=) | |
| 14 | g.28768086C>T | CA486098969 | FOXG1 | c.807C>T (p.Thr269=) | gnomAD v4 |
| 14 | g.28768087A= | CA2126000273 | FOXG1 | c.808A= (p.Thr270=) | |
| 14 | g.28768087A>C | CA389475916 | FOXG1 | c.808A>C (p.Thr270Pro) | |
| 14 | g.28768087A>G | CA389475917 | FOXG1 | c.808A>G (p.Thr270Ala) | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.28768087A>T | CA389475918 | FOXG1 | c.808A>T (p.Thr270Ser) | |
| 14 | g.28768088C>A | CA389475919 | FOXG1 | c.809C>A (p.Thr270Lys) | COSMIC |
| 14 | g.28768088C>G | CA389475920 | FOXG1 | c.809C>G (p.Thr270Arg) | |
| 14 | g.28768088C>T | CA389475921 | FOXG1 | c.809C>T (p.Thr270Met) | gnomAD v4 COSMIC |
| 14 | g.28768089G>A | CA7140631 | FOXG1 | c.810G>A (p.Thr270=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.28768089G>C | CA486098973 | FOXG1 | c.810G>C (p.Thr270=) | ClinVar gnomAD v4 |
| 14 | g.28768089G= | CA2126000274 | FOXG1 | c.810G= (p.Thr270=) | |
| 14 | g.28768089G>T | CA486098975 | FOXG1 | c.810G>T (p.Thr270=) | gnomAD v4 |
| 14 | g.28768090G>A | CA389475924 | FOXG1 | c.811G>A (p.Gly271Ser) | ClinVar dbSNP |
| 14 | g.28768090G>C | CA389475923 | FOXG1 | c.811G>C (p.Gly271Arg) | |
| 14 | g.28768090G= | CA2126000275 | FOXG1 | c.811G= (p.Gly271=) | |
| 14 | g.28768090G>T | CA389475922 | FOXG1 | c.811G>T (p.Gly271Cys) | ClinVar |
| 14 | g.28768091G>A | CA314624 | FOXG1 | c.812G>A (p.Gly271Asp) | ClinVar dbSNP COSMIC |
| 14 | g.28768091G>C | CA389475925 | FOXG1 | c.812G>C (p.Gly271Ala) | |
| 14 | g.28768091G= | CA2126000276 | FOXG1 | c.812G= (p.Gly271=) | |
| 14 | g.28768091G>T | CA389475926 | FOXG1 | c.812G>T (p.Gly271Val) | |
| 14 | g.28768092C>A | CA486098981 | FOXG1 | c.813C>A (p.Gly271=) | |
| 14 | g.28768092C= | CA2126000277 | FOXG1 | c.813C= (p.Gly271=) | |
| 14 | g.28768092C>G | CA486098982 | FOXG1 | c.813C>G (p.Gly271=) | |
| 14 | g.28768092C>T | CA486098983 | FOXG1 | c.813C>T (p.Gly271=) | dbSNP gnomAD v4 |
| 14 | g.28768093A>C | CA389475927 | FOXG1 | c.814A>C (p.Lys272Gln) | |
| 14 | g.28768093A>G | CA389475928 | FOXG1 | c.814A>G (p.Lys272Glu) | |
| 14 | g.28768093A>T | CA389475929 | FOXG1 | c.814A>T (p.Lys272Ter) | |
| 14 | g.28768093_28768100del | CA2573332464 | FOXG1 | c.814_821del (p.Lys272AlafsTer?) | ClinVar |
| 14 | g.28768094A>C | CA389475930 | FOXG1 | c.815A>C (p.Lys272Thr) | |
| 14 | g.28768094A>G | CA389475931 | FOXG1 | c.815A>G (p.Lys272Arg) | |
| 14 | g.28768094A>T | CA389475932 | FOXG1 | c.815A>T (p.Lys272Met) | |
| 14 | g.28768095G>A | CA486098988 | FOXG1 | c.816G>A (p.Lys272=) | |
| 14 | g.28768095G>C | CA389475933 | FOXG1 | c.816G>C (p.Lys272Asn) | |
| 14 | g.28768095G>T | CA389475934 | FOXG1 | c.816G>T (p.Lys272Asn) | gnomAD v4 |
| 14 | g.28768096C>A | CA389475935 | FOXG1 | c.817C>A (p.Leu273Met) | gnomAD v4 |
| 14 | g.28768096C>G | CA389475936 | FOXG1 | c.817C>G (p.Leu273Val) | |
| 14 | g.28768096C>T | CA486098991 | FOXG1 | c.817C>T (p.Leu273=) | ClinVar |
| 14 | g.28768097T>A | CA389475937 | FOXG1 | c.818T>A (p.Leu273Gln) | |
| 14 | g.28768097T>C | CA389475939 | FOXG1 | c.818T>C (p.Leu273Pro) | |
| 14 | g.28768097T>G | CA389475938 | FOXG1 | c.818T>G (p.Leu273Arg) | |
| 14 | g.28768098G>A | CA486098997 | FOXG1 | c.819G>A (p.Leu273=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28768098G>C | CA486098998 | FOXG1 | c.819G>C (p.Leu273=) | |
| 14 | g.28768098G= | CA2126000278 | FOXG1 | c.819G= (p.Leu273=) | |
| 14 | g.28768098G>T | CA486099001 | FOXG1 | c.819G>T (p.Leu273=) | gnomAD v4 |
| 14 | g.28768099C>A | CA486099003 | FOXG1 | c.820C>A (p.Arg274=) | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.28768099C= | CA2126000279 | FOXG1 | c.820C= (p.Arg274=) | |
| 14 | g.28768099C>G | CA389475940 | FOXG1 | c.820C>G (p.Arg274Gly) | |
| 14 | g.28768099C>T | CA389475941 | FOXG1 | c.820C>T (p.Arg274Trp) | gnomAD v4 COSMIC |
| 14 | g.28768100G>A | CA357167 | FOXG1 | c.821G>A (p.Arg274Gln) | ClinVar dbSNP |
| 14 | g.28768100G>C | CA389475942 | FOXG1 | c.821G>C (p.Arg274Pro) | ClinVar dbSNP |
| 14 | g.28768100G= | CA2126000280 | FOXG1 | c.821G= (p.Arg274=) | |
| 14 | g.28768100G>T | CA389475943 | FOXG1 | c.821G>T (p.Arg274Leu) | |
| 14 | g.28768101G>A | CA486099007 | FOXG1 | c.822G>A (p.Arg274=) | dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.28768101G>C | CA486099008 | FOXG1 | c.822G>C (p.Arg274=) | |
| 14 | g.28768101G= | CA2126000281 | FOXG1 | c.822G= (p.Arg274=) | |
| 14 | g.28768101G>T | CA486099009 | FOXG1 | c.822G>T (p.Arg274=) | COSMIC |
| 14 | g.28768102C>A | CA389475944 | FOXG1 | c.823C>A (p.Arg275Ser) | |
| 14 | g.28768102C>G | CA389475945 | FOXG1 | c.823C>G (p.Arg275Gly) | |
| 14 | g.28768102C>T | CA389475946 | FOXG1 | c.823C>T (p.Arg275Cys) | COSMIC |
| 14 | g.28768103G>A | CA389475947 | FOXG1 | c.824G>A (p.Arg275His) | dbSNP |
| 14 | g.28768103G>C | CA389475948 | FOXG1 | c.824G>C (p.Arg275Pro) | ClinVar dbSNP |
| 14 | g.28768103G= | CA2126000282 | FOXG1 | c.824G= (p.Arg275=) | |
| 14 | g.28768103G>T | CA389475949 | FOXG1 | c.824G>T (p.Arg275Leu) | |
| 14 | g.28768104C>A | CA486099016 | FOXG1 | c.825C>A (p.Arg275=) | |
| 14 | g.28768104C>G | CA486099015 | FOXG1 | c.825C>G (p.Arg275=) | |
| 14 | g.28768104C>T | CA486099014 | FOXG1 | c.825C>T (p.Arg275=) | gnomAD v4 COSMIC |
| 14 | g.28768105C>A | CA389475951 | FOXG1 | c.826C>A (p.Arg276Ser) | |
| 14 | g.28768105C>G | CA389475952 | FOXG1 | c.826C>G (p.Arg276Gly) | |
| 14 | g.28768105C>T | CA389475950 | FOXG1 | c.826C>T (p.Arg276Cys) | ClinVar dbSNP |
| 14 | g.28768106G>A | CA389475955 | FOXG1 | c.827G>A (p.Arg276His) | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.28768106G>C | CA389475953 | FOXG1 | c.827G>C (p.Arg276Pro) | |
| 14 | g.28768106G= | CA2126000283 | FOXG1 | c.827G= (p.Arg276=) | |
| 14 | g.28768106G>T | CA389475954 | FOXG1 | c.827G>T (p.Arg276Leu) | gnomAD v4 |
| 14 | g.28768107C>A | CA486099025 | FOXG1 | c.828C>A (p.Arg276=) | |
| 14 | g.28768107C= | CA2126000284 | FOXG1 | c.828C= (p.Arg276=) | |
| 14 | g.28768107C>G | CA486099024 | FOXG1 | c.828C>G (p.Arg276=) | |
| 14 | g.28768107C>T | CA486099022 | FOXG1 | c.828C>T (p.Arg276=) | dbSNP gnomAD v2 gnomAD v4 |
| 14 | g.28768108T>A | CA389475956 | FOXG1 | c.829T>A (p.Ser277Thr) | |
| 14 | g.28768108T>C | CA389475957 | FOXG1 | c.829T>C (p.Ser277Pro) | |
| 14 | g.28768108T>G | CA389475958 | FOXG1 | c.829T>G (p.Ser277Ala) | |
| 14 | g.28768109C>A | CA389475959 | FOXG1 | c.830C>A (p.Ser277Tyr) | |
| 14 | g.28768109C>G | CA389475960 | FOXG1 | c.830C>G (p.Ser277Cys) | |
| 14 | g.28768109C>T | CA389475961 | FOXG1 | c.830C>T (p.Ser277Phe) | |
| 14 | g.28768110C>A | CA486099033 | FOXG1 | c.831C>A (p.Ser277=) | |
| 14 | g.28768110C>G | CA486099035 | FOXG1 | c.831C>G (p.Ser277=) | |
| 14 | g.28768110C>T | CA486099034 | FOXG1 | c.831C>T (p.Ser277=) |