| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 14 | g.28767662_28767772del | CA2624399051 | FOXG1 | c.383_493del (p.Gly128_Lys164del) | gnomAD v4 |
| 14 | g.28767686_28767737del | CA891844335 | FOXG1 | c.407_458del (p.Glu136GlyfsTer?) | ClinVar dbSNP |
| 14 | g.28767729_28767734dup | CA7140600 | FOXG1 | c.450_455dup (p.Gly152_Gly153insAlaGly) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28767732_28767733delinsCG | CA2125999475 | FOXG1 | c.453_454delinsCG (p.Ala151=) | |
| 14 | g.28767733G>A | CA389475126 | FOXG1 | c.454G>A (p.Gly152Arg) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28767733G>C | CA389475127 | FOXG1 | c.454G>C (p.Gly152Arg) | dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.28767733G= | CA2125999487 | FOXG1 | c.454G= (p.Gly152=) | |
| 14 | g.28767733G>T | CA389475128 | FOXG1 | c.454G>T (p.Gly152Trp) | ClinVar gnomAD v4 |
| 14 | g.28767739dup | CA199435 | FOXG1 | c.460dup (p.Glu154GlyfsTer?) | ClinVar dbSNP gnomAD v4 COSMIC |
| 14 | g.28767739del | CA357157 | FOXG1 | c.460del (p.Glu154ArgfsTer?) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 14 | g.28767738_28767739del | CA2697553885 | FOXG1 | c.459_460del (p.Glu154GlyfsTer?) | ClinVar |
| 14 | g.28767734G>A | CA314604 | FOXG1 | c.455G>A (p.Gly152Glu) | ClinVar dbSNP gnomAD v4 |
| 14 | g.28767734G>C | CA389475129 | FOXG1 | c.455G>C (p.Gly152Ala) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28767734G= | CA2125999498 | FOXG1 | c.455G= (p.Gly152=) | |
| 14 | g.28767734G>T | CA389475130 | FOXG1 | c.455G>T (p.Gly152Val) | ClinVar dbSNP |
| 14 | g.28767735G>A | CA7140603 | FOXG1 | c.456G>A (p.Gly152=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28767735G>C | CA7140604 | FOXG1 | c.456G>C (p.Gly152=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28767735G= | CA2125999505 | FOXG1 | c.456G= (p.Gly152=) | |
| 14 | g.28767735G>T | CA172183 | FOXG1 | c.456G>T (p.Gly152=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28767736G>A | CA389475131 | FOXG1 | c.457G>A (p.Gly153Arg) | ClinVar dbSNP |
| 14 | g.28767736G>C | CA389475132 | FOXG1 | c.457G>C (p.Gly153Arg) | |
| 14 | g.28767736G= | CA2125999512 | FOXG1 | c.457G= (p.Gly153=) | |
| 14 | g.28767736G>T | CA389475133 | FOXG1 | c.457G>T (p.Gly153Trp) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.28767737G>A | CA389475134 | FOXG1 | c.458G>A (p.Gly153Glu) | gnomAD v4 |
| 14 | g.28767737G>C | CA389475135 | FOXG1 | c.458G>C (p.Gly153Ala) | |
| 14 | g.28767737G= | CA2125999518 | FOXG1 | c.458G= (p.Gly153=) | |
| 14 | g.28767737G>T | CA389475136 | FOXG1 | c.458G>T (p.Gly153Val) | ClinVar dbSNP gnomAD v4 COSMIC |
| 14 | g.28767737_28767740delinsGGGA | CA2125999515 | FOXG1 | c.458_461delinsGGGA (p.Gly153=) | |
| 14 | g.28767738G>A | CA486098217 | FOXG1 | c.459G>A (p.Gly153=) | ClinVar dbSNP gnomAD v4 |
| 14 | g.28767738G>C | CA486098218 | FOXG1 | c.459G>C (p.Gly153=) | |
| 14 | g.28767738G= | CA1139532150 | FOXG1 | c.459G= (p.Gly153=) | |
| 14 | g.28767738G>T | CA16606977 | FOXG1 | c.459G>T (p.Gly153=) | ClinVar dbSNP gnomAD v4 |
| 14 | g.28767742_28767744del | CA613324873 | FOXG1 | c.463_465del (p.Glu155del) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.28767739G>A | CA389475137 | FOXG1 | c.460G>A (p.Glu154Lys) | gnomAD v4 |
| 14 | g.28767739G>C | CA389475138 | FOXG1 | c.460G>C (p.Glu154Gln) | |
| 14 | g.28767739G= | CA2125999531 | FOXG1 | c.460G= (p.Glu154=) | |
| 14 | g.28767739G>T | CA16606551 | FOXG1 | c.460G>T (p.Glu154Ter) | ClinVar dbSNP |
| 14 | g.28767740A= | CA2125999536 | FOXG1 | c.461A= (p.Glu154=) | |
| 14 | g.28767740A>C | CA389475139 | FOXG1 | c.461A>C (p.Glu154Ala) | |
| 14 | g.28767740A>G | CA389475141 | FOXG1 | c.461A>G (p.Glu154Gly) | dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.28767740A>T | CA389475140 | FOXG1 | c.461A>T (p.Glu154Val) | |
| 14 | g.28767741G>A | CA486098224 | FOXG1 | c.462G>A (p.Glu154=) | ClinVar dbSNP gnomAD v4 |
| 14 | g.28767741G>C | CA389475142 | FOXG1 | c.462G>C (p.Glu154Asp) | |
| 14 | g.28767741G= | CA2125999537 | FOXG1 | c.462G= (p.Glu154=) | |
| 14 | g.28767741G>T | CA389475143 | FOXG1 | c.462G>T (p.Glu154Asp) | |
| 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) |