Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.28767412_28767748delinsACCCACCGCCCC | CA2766230034 | FOXG1 | c.133_469delinsACCCACCGCCCC (p.Pro45ThrfsTer?) | |
14 | g.28767662_28767772del | CA2624399051 | FOXG1 | c.383_493del (p.Gly128_Lys164del) | gnomAD v4 |
14 | g.28767742_28767744del | CA613324873 | FOXG1 | c.463_465del (p.Glu155del) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.28767742G>A | CA389475144 | FOXG1 | c.463G>A (p.Glu155Lys) | COSMIC |
14 | g.28767742G>C | CA389475145 | FOXG1 | c.463G>C (p.Glu155Gln) | |
14 | g.28767742G>T | CA389475146 | FOXG1 | c.463G>T (p.Glu155Ter) | |
14 | g.28767742_28767745delinsGAGA | CA2125999539 | FOXG1 | c.463_466delinsGAGA (p.Glu155=) | |
14 | g.28767743A>C | CA389475147 | FOXG1 | c.464A>C (p.Glu155Ala) | |
14 | g.28767743A>G | CA389475148 | FOXG1 | c.464A>G (p.Glu155Gly) | |
14 | g.28767743A>T | CA389475149 | FOXG1 | c.464A>T (p.Glu155Val) | |
14 | g.28767748_28767750del | CA613324874 | FOXG1 | c.469_471del (p.Lys157del) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
14 | g.28767744G>A | CA486098230 | FOXG1 | c.465G>A (p.Glu155=) | |
14 | g.28767744G>C | CA389475150 | FOXG1 | c.465G>C (p.Glu155Asp) | |
14 | g.28767744G>T | CA389475151 | FOXG1 | c.465G>T (p.Glu155Asp) | |
14 | g.28767745A= | CA2125999544 | FOXG1 | c.466A= (p.Lys156=) | |
14 | g.28767745A>C | CA389475152 | FOXG1 | c.466A>C (p.Lys156Gln) | |
14 | g.28767745A>G | CA389475154 | FOXG1 | c.466A>G (p.Lys156Glu) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.28767745A>T | CA389475153 | FOXG1 | c.466A>T (p.Lys156Ter) | |
14 | g.28767746A>C | CA389475155 | FOXG1 | c.467A>C (p.Lys156Thr) | |
14 | g.28767746A>G | CA389475157 | FOXG1 | c.467A>G (p.Lys156Arg) | |
14 | g.28767746A>T | CA389475156 | FOXG1 | c.467A>T (p.Lys156Met) | |
14 | g.28767747G>A | CA486098235 | FOXG1 | c.468G>A (p.Lys156=) | dbSNP |
14 | g.28767747G>C | CA389475158 | FOXG1 | c.468G>C (p.Lys156Asn) | gnomAD v4 |
14 | g.28767747G= | CA2125999546 | FOXG1 | c.468G= (p.Lys156=) | |
14 | g.28767747G>T | CA389475159 | FOXG1 | c.468G>T (p.Lys156Asn) | |
14 | g.28767748A>C | CA389475160 | FOXG1 | c.469A>C (p.Lys157Gln) | |
14 | g.28767748A>G | CA389475161 | FOXG1 | c.469A>G (p.Lys157Glu) | |
14 | g.28767748A>T | CA389475162 | FOXG1 | c.469A>T (p.Lys157Ter) | ClinVar dbSNP |
14 | g.28767749A= | CA2125999549 | FOXG1 | c.470A= (p.Lys157=) | |
14 | g.28767749A>C | CA389475163 | FOXG1 | c.470A>C (p.Lys157Thr) | |
14 | g.28767749A>G | CA389475164 | FOXG1 | c.470A>G (p.Lys157Arg) | dbSNP gnomAD v2 gnomAD v4 |
14 | g.28767749A>T | CA389475165 | FOXG1 | c.470A>T (p.Lys157Met) | dbSNP gnomAD v4 |
14 | g.28767750G>A | CA486098243 | FOXG1 | c.471G>A (p.Lys157=) | ClinVar dbSNP |
14 | g.28767750G>C | CA389475166 | FOXG1 | c.471G>C (p.Lys157Asn) | ClinVar dbSNP |
14 | g.28767750G= | CA2125999556 | FOXG1 | c.471G= (p.Lys157=) | |
14 | g.28767750G>T | CA222858 | FOXG1 | c.471G>T (p.Lys157Asn) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
14 | g.28767754del | CA2695219191 | FOXG1 | c.475del (p.Ala159ArgfsTer?) | |
14 | g.28767751G>A | CA389475167 | FOXG1 | c.472G>A (p.Gly158Arg) | |
14 | g.28767751G>C | CA389475168 | FOXG1 | c.472G>C (p.Gly158Arg) | |
14 | g.28767751G>T | CA389475169 | FOXG1 | c.472G>T (p.Gly158Trp) | |
14 | g.28767752G>A | CA389475170 | FOXG1 | c.473G>A (p.Gly158Glu) | |
14 | g.28767752G>C | CA389475172 | FOXG1 | c.473G>C (p.Gly158Ala) | |
14 | g.28767752G>T | CA389475171 | FOXG1 | c.473G>T (p.Gly158Val) | |
14 | g.28767758_28767767del | CA2695219192 | FOXG1 | c.479_488del (p.Gly160AlafsTer29) | |
14 | g.28767753G>A | CA486098248 | FOXG1 | c.474G>A (p.Gly158=) | |
14 | g.28767753G>C | CA486098249 | FOXG1 | c.474G>C (p.Gly158=) | |
14 | g.28767753G>T | CA486098250 | FOXG1 | c.474G>T (p.Gly158=) | |
14 | g.28767754G>A | CA389475173 | FOXG1 | c.475G>A (p.Ala159Thr) | ClinVar |
14 | g.28767754G>C | CA389475174 | FOXG1 | c.475G>C (p.Ala159Pro) | |
14 | g.28767754G= | CA2125999565 | FOXG1 | c.475G= (p.Ala159=) |