Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.28768004_28768010dup | CA2580088018 | FOXG1 | c.725_731dup (p.His245AlafsTer?) | ClinVar |
14 | g.28768007C>A | CA389475737 | FOXG1 | c.728C>A (p.Pro243Gln) | |
14 | g.28768007C= | CA2126000078 | FOXG1 | c.728C= (p.Pro243=) | |
14 | g.28768007C>G | CA389475738 | FOXG1 | c.728C>G (p.Pro243Arg) | dbSNP gnomAD v2 gnomAD v4 |
14 | g.28768007C>T | CA389475740 | FOXG1 | c.728C>T (p.Pro243Leu) | COSMIC |
14 | g.28768008G>A | CA486098849 | FOXG1 | c.729G>A (p.Pro243=) | ClinVar dbSNP COSMIC |
14 | g.28768008G>C | CA7140627 | FOXG1 | c.729G>C (p.Pro243=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
14 | g.28768008G= | CA2126000084 | FOXG1 | c.729G= (p.Pro243=) | |
14 | g.28768008G>T | CA486098850 | FOXG1 | c.729G>T (p.Pro243=) | |
14 | g.28768009C>A | CA389475741 | FOXG1 | c.730C>A (p.Arg244Ser) | gnomAD v3 gnomAD v4 |
14 | g.28768009C= | CA2126000087 | FOXG1 | c.730C= (p.Arg244=) | |
14 | g.28768009C>G | CA389475742 | FOXG1 | c.730C>G (p.Arg244Gly) | |
14 | g.28768009C>T | CA199444 | FOXG1 | c.730C>T (p.Arg244Cys) | ClinVar dbSNP COSMIC |
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) |