Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.28768203G>A | CA123555 | FOXG1 | c.924G>A (p.Trp308Ter) | ClinVar dbSNP |
14 | g.28768203G>C | CA389476153 | FOXG1 | c.924G>C (p.Trp308Cys) | COSMIC |
14 | g.28768203G= | CA2126000321 | FOXG1 | c.924G= (p.Trp308=) | |
14 | g.28768203G>T | CA389476152 | FOXG1 | c.924G>T (p.Trp308Cys) | |
14 | g.28768204C>A | CA389476154 | FOXG1 | c.925C>A (p.Pro309Thr) | |
14 | g.28768204C= | CA2126000322 | FOXG1 | c.925C= (p.Pro309=) | |
14 | g.28768204C>G | CA389476155 | FOXG1 | c.925C>G (p.Pro309Ala) | |
14 | g.28768204C>T | CA389476156 | FOXG1 | c.925C>T (p.Pro309Ser) | dbSNP gnomAD v2 gnomAD v4 |
14 | g.28768205C>A | CA389476157 | FOXG1 | c.926C>A (p.Pro309His) | |
14 | g.28768205C= | CA2126000323 | FOXG1 | c.926C= (p.Pro309=) | |
14 | g.28768205C>G | CA258396587 | FOXG1 | c.926C>G (p.Pro309Arg) | dbSNP |
14 | g.28768205C>T | CA389476158 | FOXG1 | c.926C>T (p.Pro309Leu) | |
14 | g.28768206C>A | CA486098300 | FOXG1 | c.927C>A (p.Pro309=) | gnomAD v4 |
14 | g.28768206C= | CA2126000324 | FOXG1 | c.927C= (p.Pro309=) | |
14 | g.28768206C>G | CA486098299 | FOXG1 | c.927C>G (p.Pro309=) | |
14 | g.28768206C>T | CA486098298 | FOXG1 | c.927C>T (p.Pro309=) | dbSNP gnomAD v3 gnomAD v4 |
14 | g.28768207A>C | CA389476159 | FOXG1 | c.928A>C (p.Met310Leu) | gnomAD v4 |
14 | g.28768207A>G | CA389476160 | FOXG1 | c.928A>G (p.Met310Val) | |
14 | g.28768207A>T | CA389476161 | FOXG1 | c.928A>T (p.Met310Leu) | |
14 | g.28768208T>A | CA389476163 | FOXG1 | c.929T>A (p.Met310Lys) | |
14 | g.28768208T>C | CA389476164 | FOXG1 | c.929T>C (p.Met310Thr) | |
14 | g.28768208T>G | CA389476162 | FOXG1 | c.929T>G (p.Met310Arg) | |
14 | g.28768209G>A | CA389476165 | FOXG1 | c.930G>A (p.Met310Ile) | |
14 | g.28768209G>C | CA389476166 | FOXG1 | c.930G>C (p.Met310Ile) | |
14 | g.28768209G>T | CA389476167 | FOXG1 | c.930G>T (p.Met310Ile) | |
14 | g.28768210T>A | CA389476168 | FOXG1 | c.931T>A (p.Ser311Thr) | |
14 | g.28768210T>C | CA389476169 | FOXG1 | c.931T>C (p.Ser311Pro) | |
14 | g.28768210T>G | CA389476170 | FOXG1 | c.931T>G (p.Ser311Ala) | |
14 | g.28768211C>A | CA389476171 | FOXG1 | c.932C>A (p.Ser311Ter) | dbSNP |
14 | g.28768211C>G | CA389476172 | FOXG1 | c.932C>G (p.Ser311Trp) | |
14 | g.28768211C>T | CA389476173 | FOXG1 | c.932C>T (p.Ser311Leu) | |
14 | g.28768212G>A | CA486098302 | FOXG1 | c.933G>A (p.Ser311=) | ClinVar |
14 | g.28768212G>C | CA486098304 | FOXG1 | c.933G>C (p.Ser311=) | gnomAD v4 |
14 | g.28768212G= | CA2126000325 | FOXG1 | c.933G= (p.Ser311=) | |
14 | g.28768212G>T | CA486098303 | FOXG1 | c.933G>T (p.Ser311=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
14 | g.28768213C>A | CA389476174 | FOXG1 | c.934C>A (p.Pro312Thr) | |
14 | g.28768213C>G | CA389476175 | FOXG1 | c.934C>G (p.Pro312Ala) | |
14 | g.28768213C>T | CA389476176 | FOXG1 | c.934C>T (p.Pro312Ser) | gnomAD v4 |
14 | g.28768214C>A | CA389476179 | FOXG1 | c.935C>A (p.Pro312His) | |
14 | g.28768214C>G | CA389476177 | FOXG1 | c.935C>G (p.Pro312Arg) | |
14 | g.28768214C>T | CA389476178 | FOXG1 | c.935C>T (p.Pro312Leu) | |
14 | g.28768215C>A | CA486098308 | FOXG1 | c.936C>A (p.Pro312=) | |
14 | g.28768215C= | CA2126000326 | FOXG1 | c.936C= (p.Pro312=) | |
14 | g.28768215C>G | CA486098309 | FOXG1 | c.936C>G (p.Pro312=) | gnomAD v4 |
14 | g.28768215C>T | CA486098310 | FOXG1 | c.936C>T (p.Pro312=) | ClinVar dbSNP gnomAD v4 |
14 | g.28768216T>A | CA389476180 | FOXG1 | c.937T>A (p.Phe313Ile) | |
14 | g.28768216T>C | CA389476181 | FOXG1 | c.937T>C (p.Phe313Leu) | gnomAD v4 |
14 | g.28768216T>G | CA389476182 | FOXG1 | c.937T>G (p.Phe313Val) | |
14 | g.28768217T>A | CA389476183 | FOXG1 | c.938T>A (p.Phe313Tyr) | |
14 | g.28768217T>C | CA389476184 | FOXG1 | c.938T>C (p.Phe313Ser) |