Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.28767412_28767748delinsACCCACCGCCCCCA2766230034FOXG1c.133_469delinsACCCACCGCCCC (p.Pro45ThrfsTer?)
14g.28767517_28767625delCA2801003621FOXG1c.238_346del (p.Pro80TrpfsTer?)
14g.28767603_28767624delCA2624398855FOXG1c.324_345del (p.Pro109TrpfsTer?)
gnomAD v4
14g.28767615_28767624delCA1139663424FOXG1c.336_345del (p.Ala113TrpfsTer?)
ClinVar
14g.28767620_28767631delCA2624398965FOXG1c.341_352del (p.Ala114_Asp117del)
gnomAD v4
14g.28767622G>ACA389474901FOXG1c.343G>A (p.Ala115Thr)
gnomAD v4
14g.28767622G>CCA389474902FOXG1c.343G>C (p.Ala115Pro)
14g.28767622G>TCA389474903FOXG1c.343G>T (p.Ala115Ser)
gnomAD v4
14g.28767623C>ACA389474904FOXG1c.344C>A (p.Ala115Asp)
gnomAD v4
14g.28767623C=CA2125999201FOXG1c.344C= (p.Ala115=)
14g.28767623C>GCA258396560FOXG1c.344C>G (p.Ala115Gly)
dbSNP
14g.28767623C>TCA314580FOXG1c.344C>T (p.Ala115Val)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.28767624C>ACA486098290FOXG1c.345C>A (p.Ala115=)
14g.28767624C>GCA486098291FOXG1c.345C>G (p.Ala115=)
14g.28767624C>TCA486098292FOXG1c.345C>T (p.Ala115=)
gnomAD v4
14g.28767625C>ACA389474906FOXG1c.346C>A (p.Leu116Met)
gnomAD v4
14g.28767625C>GCA389474905FOXG1c.346C>G (p.Leu116Val)
14g.28767625C>TCA486098294FOXG1c.346C>T (p.Leu116=)
14g.28767626T>ACA389474907FOXG1c.347T>A (p.Leu116Gln)
gnomAD v4
14g.28767626T>CCA389474908FOXG1c.347T>C (p.Leu116Pro)
ClinVar dbSNP gnomAD v4
14g.28767626T>GCA389474909FOXG1c.347T>G (p.Leu116Arg)
ClinVar
14g.28767626T=CA2125999207FOXG1c.347T= (p.Leu116=)
14g.28767627G>ACA486098295FOXG1c.348G>A (p.Leu116=)
gnomAD v4
14g.28767627G>CCA486098296FOXG1c.348G>C (p.Leu116=)
14g.28767627G>TCA486098297FOXG1c.348G>T (p.Leu116=)
gnomAD v4
14g.28767634_28767648delCA2624398994FOXG1c.355_369del (p.Ala119_Gly123del)
gnomAD v4
14g.28767628G>ACA389474910FOXG1c.349G>A (p.Asp117Asn)
dbSNP gnomAD v2 gnomAD v4
14g.28767628G>CCA389474911FOXG1c.349G>C (p.Asp117His)
14g.28767628G=CA2125999211FOXG1c.349G= (p.Asp117=)
14g.28767628G>TCA389474912FOXG1c.349G>T (p.Asp117Tyr)
gnomAD v4
14g.28767629A>CCA389474913FOXG1c.350A>C (p.Asp117Ala)
14g.28767629A>GCA389474915FOXG1c.350A>G (p.Asp117Gly)
ClinVar
14g.28767629A>TCA389474914FOXG1c.350A>T (p.Asp117Val)
14g.28767630C>ACA389474916FOXG1c.351C>A (p.Asp117Glu)
gnomAD v4
14g.28767630C>GCA389474917FOXG1c.351C>G (p.Asp117Glu)
14g.28767630C>TCA486098301FOXG1c.351C>T (p.Asp117=)
ClinVar dbSNP gnomAD v4
14g.28767631G>ACA389474918FOXG1c.352G>A (p.Gly118Arg)
ClinVar dbSNP gnomAD v2 gnomAD v4
14g.28767631G>CCA389474919FOXG1c.352G>C (p.Gly118Arg)
gnomAD v4
14g.28767631G=CA2125999214FOXG1c.352G= (p.Gly118=)
14g.28767631G>TCA389474920FOXG1c.352G>T (p.Gly118Trp)
gnomAD v4
14g.28767632G>ACA389474921FOXG1c.353G>A (p.Gly118Glu)
gnomAD v4
14g.28767632G>CCA389474922FOXG1c.353G>C (p.Gly118Ala)
14g.28767632G>TCA389474923FOXG1c.353G>T (p.Gly118Val)
gnomAD v4
14g.28767633G>ACA486098305FOXG1c.354G>A (p.Gly118=)
dbSNP gnomAD v2 gnomAD v4
14g.28767633G>CCA486098306FOXG1c.354G>C (p.Gly118=)
ClinVar gnomAD v4
14g.28767633G=CA2125999217FOXG1c.354G= (p.Gly118=)
14g.28767633G>TCA486098307FOXG1c.354G>T (p.Gly118=)
14g.28767634G>ACA389474924FOXG1c.355G>A (p.Ala119Thr)
gnomAD v4
14g.28767634G>CCA389474925FOXG1c.355G>C (p.Ala119Pro)
14g.28767634G=CA2125999220FOXG1c.355G= (p.Ala119=)
14g.28767634G>TCA314602FOXG1c.355G>T (p.Ala119Ser)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.28767635delCA2573149900FOXG1c.356del (p.Ala119ValfsTer?)
ClinVar dbSNP
14g.28767635C>ACA389474926FOXG1c.356C>A (p.Ala119Asp)
gnomAD v4
14g.28767635C>GCA389474928FOXG1c.356C>G (p.Ala119Gly)
14g.28767635C>TCA389474927FOXG1c.356C>T (p.Ala119Val)
gnomAD v4
14g.28767636T>ACA486098311FOXG1c.357T>A (p.Ala119=)
14g.28767636T>CCA486098312FOXG1c.357T>C (p.Ala119=)
14g.28767636T>GCA486098313FOXG1c.357T>G (p.Ala119=)
dbSNP
14g.28767636T=CA2125999222FOXG1c.357T= (p.Ala119=)
14g.28767637A>CCA389474929FOXG1c.358A>C (p.Lys120Gln)
14g.28767637A>GCA389474931FOXG1c.358A>G (p.Lys120Glu)
14g.28767637A>TCA389474930FOXG1c.358A>T (p.Lys120Ter)
14g.28767639delCA2624399018FOXG1c.360del (p.Ala121ArgfsTer?)
gnomAD v4
14g.28767638A=CA2125999224FOXG1c.359A= (p.Lys120=)
14g.28767638A>CCA389474932FOXG1c.359A>C (p.Lys120Thr)
14g.28767638A>GCA389474933FOXG1c.359A>G (p.Lys120Arg)
14g.28767638A>TCA389474934FOXG1c.359A>T (p.Lys120Ile)
dbSNP gnomAD v2 gnomAD v4
14g.28767639A>CCA389474935FOXG1c.360A>C (p.Lys120Asn)
14g.28767639A>GCA486098319FOXG1c.360A>G (p.Lys120=)
gnomAD v4
14g.28767639A>TCA389474936FOXG1c.360A>T (p.Lys120Asn)
14g.28767640G>ACA389474937FOXG1c.361G>A (p.Ala121Thr)
14g.28767640G>CCA389474938FOXG1c.361G>C (p.Ala121Pro)
ClinVar dbSNP gnomAD v4
14g.28767640G=CA2125999227FOXG1c.361G= (p.Ala121=)
14g.28767640G>TCA389474939FOXG1c.361G>T (p.Ala121Ser)
dbSNP
14g.28767641C>ACA389474940FOXG1c.362C>A (p.Ala121Glu)
gnomAD v4
14g.28767641C>GCA389474941FOXG1c.362C>G (p.Ala121Gly)
ClinVar dbSNP
14g.28767641C>TCA389474942FOXG1c.362C>T (p.Ala121Val)
gnomAD v4
14g.28767642G>ACA486098330FOXG1c.363G>A (p.Ala121=)
dbSNP gnomAD v3 gnomAD v4
14g.28767642G>CCA486098327FOXG1c.363G>C (p.Ala121=)
dbSNP gnomAD v4
14g.28767642G=CA2125999229FOXG1c.363G= (p.Ala121=)
14g.28767642G>TCA486098325FOXG1c.363G>T (p.Ala121=)
14g.28767643G>ACA389474945FOXG1c.364G>A (p.Asp122Asn)
14g.28767643G>CCA389474943FOXG1c.364G>C (p.Asp122His)
14g.28767643G>TCA389474944FOXG1c.364G>T (p.Asp122Tyr)
14g.28767644A>CCA389474946FOXG1c.365A>C (p.Asp122Ala)
gnomAD v4
14g.28767644A>GCA389474947FOXG1c.365A>G (p.Asp122Gly)
14g.28767644A>TCA389474948FOXG1c.365A>T (p.Asp122Val)
14g.28767645C>ACA389474949FOXG1c.366C>A (p.Asp122Glu)
dbSNP gnomAD v3 gnomAD v4
14g.28767645C=CA2125999231FOXG1c.366C= (p.Asp122=)
14g.28767645C>GCA389474950FOXG1c.366C>G (p.Asp122Glu)
14g.28767645C>TCA486098095FOXG1c.366C>T (p.Asp122=)
gnomAD v4
14g.28767646G>ACA258396561FOXG1c.367G>A (p.Gly123Arg)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.28767646G>CCA7140595FOXG1c.367G>C (p.Gly123Arg)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.28767646G=CA2125999233FOXG1c.367G= (p.Gly123=)
14g.28767646G>TCA389474951FOXG1c.367G>T (p.Gly123Trp)
14g.28767647G>ACA389474952FOXG1c.368G>A (p.Gly123Glu)
14g.28767647G>CCA389474953FOXG1c.368G>C (p.Gly123Ala)
14g.28767647G>TCA389474954FOXG1c.368G>T (p.Gly123Val)
gnomAD v4
14g.28767648G>ACA486098099FOXG1c.369G>A (p.Gly123=)
gnomAD v4
14g.28767648G>CCA486098100FOXG1c.369G>C (p.Gly123=)
14g.28767648G>TCA486098102FOXG1c.369G>T (p.Gly123=)
gnomAD v4
14g.28767649C>ACA389474956FOXG1c.370C>A (p.Leu124Met)
14g.28767649C>GCA389474955FOXG1c.370C>G (p.Leu124Val)
14g.28767649C>TCA486098105FOXG1c.370C>T (p.Leu124=)
gnomAD v4
14g.28767650T>ACA389474957FOXG1c.371T>A (p.Leu124Gln)
gnomAD v4
14g.28767650T>CCA389474958FOXG1c.371T>C (p.Leu124Pro)
COSMIC
14g.28767650T>GCA389474959FOXG1c.371T>G (p.Leu124Arg)
14g.28767650_28767668delinsTGGGCGGCAAGGGCGAGCCCA2125999237FOXG1c.371_389delinsTGGGCGGCAAGGGCGAGCC (p.Leu124=)
14g.28767651G>ACA486098106FOXG1c.372G>A (p.Leu124=)
14g.28767651G>CCA486098107FOXG1c.372G>C (p.Leu124=)
14g.28767651G>TCA486098108FOXG1c.372G>T (p.Leu124=)
COSMIC
14g.28767658_28767675dupCA2624399050FOXG1c.379_396dup (p.Gly132_Gly133insLysGlyGluProGlyGly)
gnomAD v4
14g.28767658_28767675delCA2125999239FOXG1c.379_396del (p.Lys127_Gly132del)
ClinVar dbSNP gnomAD v4
14g.28767662_28767772delCA2624399051FOXG1c.383_493del (p.Gly128_Lys164del)
gnomAD v4
14g.28767652G>ACA389474960FOXG1c.373G>A (p.Gly125Ser)
14g.28767652G>CCA389474961FOXG1c.373G>C (p.Gly125Arg)
14g.28767652G>TCA389474962FOXG1c.373G>T (p.Gly125Cys)
14g.28767653G>ACA389474963FOXG1c.374G>A (p.Gly125Asp)
14g.28767653G>CCA389474964FOXG1c.374G>C (p.Gly125Ala)
14g.28767653G>TCA389474965FOXG1c.374G>T (p.Gly125Val)
14g.28767654C>ACA486098110FOXG1c.375C>A (p.Gly125=)
ClinVar dbSNP
14g.28767654C=CA2125999242FOXG1c.375C= (p.Gly125=)
14g.28767654C>GCA486098111FOXG1c.375C>G (p.Gly125=)
14g.28767654C>TCA486098112FOXG1c.375C>T (p.Gly125=)
dbSNP gnomAD v2 gnomAD v4
14g.28767655G>ACA314582FOXG1c.376G>A (p.Gly126Ser)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.28767655G>CCA389474966FOXG1c.376G>C (p.Gly126Arg)
14g.28767655G=CA2125999245FOXG1c.376G= (p.Gly126=)
14g.28767655G>TCA389474967FOXG1c.376G>T (p.Gly126Cys)
14g.28767656G>ACA389474970FOXG1c.377G>A (p.Gly126Asp)
dbSNP gnomAD v4
14g.28767656G>CCA389474969FOXG1c.377G>C (p.Gly126Ala)
14g.28767656G=CA2125999249FOXG1c.377G= (p.Gly126=)
14g.28767656G>TCA389474968FOXG1c.377G>T (p.Gly126Val)
gnomAD v4
14g.28767657C>ACA486098113FOXG1c.378C>A (p.Gly126=)
14g.28767657C=CA2125999255FOXG1c.378C= (p.Gly126=)
14g.28767657C>GCA486098114FOXG1c.378C>G (p.Gly126=)
14g.28767657C>TCA258396562FOXG1c.378C>T (p.Gly126=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.28767658A>CCA389474971FOXG1c.379A>C (p.Lys127Gln)
14g.28767658A>GCA389474972FOXG1c.379A>G (p.Lys127Glu)
ClinVar
14g.28767658A>TCA389474973FOXG1c.379A>T (p.Lys127Ter)
14g.28767659A=CA2125999266FOXG1c.380A= (p.Lys127=)
14g.28767659A>CCA389474974FOXG1c.380A>C (p.Lys127Thr)
14g.28767659A>GCA258396563FOXG1c.380A>G (p.Lys127Arg)
dbSNP
14g.28767659A>TCA389474975FOXG1c.380A>T (p.Lys127Met)
14g.28767660G>ACA486098119FOXG1c.381G>A (p.Lys127=)
dbSNP gnomAD v3 gnomAD v4
14g.28767660G>CCA389474976FOXG1c.381G>C (p.Lys127Asn)
gnomAD v4
14g.28767660G=CA2125999273FOXG1c.381G= (p.Lys127=)
14g.28767660G>TCA389474977FOXG1c.381G>T (p.Lys127Asn)
14g.28767662dupCA314640FOXG1c.383dup (p.Glu129ArgfsTer?)
ClinVar dbSNP
14g.28767661G>ACA389474978FOXG1c.382G>A (p.Gly128Ser)
gnomAD v4
14g.28767661G>CCA389474979FOXG1c.382G>C (p.Gly128Arg)
14g.28767661G=CA2125999280FOXG1c.382G= (p.Gly128=)
14g.28767661G>TCA258396564FOXG1c.382G>T (p.Gly128Cys)
ClinVar dbSNP gnomAD v3 gnomAD v4
14g.28767665_28767676dupCA314584FOXG1c.386_397dup (p.Gly132_Gly133insGluProGlyGly)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.28767662G>ACA389474982FOXG1c.383G>A (p.Gly128Asp)
dbSNP
14g.28767662G>CCA389474981FOXG1c.383G>C (p.Gly128Ala)
14g.28767662G=CA2125999285FOXG1c.383G= (p.Gly128=)
14g.28767662G>TCA389474980FOXG1c.383G>T (p.Gly128Val)
14g.28767663C>ACA486098124FOXG1c.384C>A (p.Gly128=)
gnomAD v4
14g.28767663C=CA2125999287FOXG1c.384C= (p.Gly128=)
14g.28767663C>GCA258396565FOXG1c.384C>G (p.Gly128=)
dbSNP gnomAD v4
14g.28767663C>TCA486098123FOXG1c.384C>T (p.Gly128=)
gnomAD v4
14g.28767664delCA2573053890FOXG1c.385del (p.Glu129SerfsTer?)
ClinVar dbSNP
14g.28767664G>ACA389474983FOXG1c.385G>A (p.Glu129Lys)
14g.28767664G>CCA389474985FOXG1c.385G>C (p.Glu129Gln)
14g.28767664G=CA2125999292FOXG1c.385G= (p.Glu129=)
14g.28767664G>TCA389474984FOXG1c.385G>T (p.Glu129Ter)
ClinVar dbSNP
14g.28767665A>CCA389474986FOXG1c.386A>C (p.Glu129Ala)
14g.28767665A>GCA389474987FOXG1c.386A>G (p.Glu129Gly)
14g.28767665A>TCA389474988FOXG1c.386A>T (p.Glu129Val)
14g.28767666G>ACA486098126FOXG1c.387G>A (p.Glu129=)
14g.28767666G>CCA389474989FOXG1c.387G>C (p.Glu129Asp)
14g.28767666G>TCA389474990FOXG1c.387G>T (p.Glu129Asp)
14g.28767667C>ACA389474991FOXG1c.388C>A (p.Pro130Thr)
gnomAD v4
14g.28767667C>GCA389474992FOXG1c.388C>G (p.Pro130Ala)
14g.28767667C>TCA389474993FOXG1c.388C>T (p.Pro130Ser)
gnomAD v4
14g.28767668delCA2580087997FOXG1c.389del (p.Pro130ArgfsTer?)
ClinVar
14g.28767668C>ACA389474994FOXG1c.389C>A (p.Pro130Gln)
gnomAD v4
14g.28767668C>GCA389474995FOXG1c.389C>G (p.Pro130Arg)
gnomAD v4
14g.28767668C>TCA389474996FOXG1c.389C>T (p.Pro130Leu)
gnomAD v4
14g.28767669G>ACA258396566FOXG1c.390G>A (p.Pro130=)
ClinVar dbSNP gnomAD v3 gnomAD v4
14g.28767669G>CCA486098128FOXG1c.390G>C (p.Pro130=)
14g.28767669G=CA2125999295FOXG1c.390G= (p.Pro130=)
14g.28767669G>TCA486098129FOXG1c.390G>T (p.Pro130=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.28767671delCA2695219190FOXG1c.392del (p.Gly131AlafsTer?)
14g.28767670G>ACA389474997FOXG1c.391G>A (p.Gly131Ser)
gnomAD v4
14g.28767670G>CCA389474998FOXG1c.391G>C (p.Gly131Arg)
14g.28767670G>TCA389474999FOXG1c.391G>T (p.Gly131Cys)
14g.28767671G>ACA389475000FOXG1c.392G>A (p.Gly131Asp)
14g.28767671G>CCA389475002FOXG1c.392G>C (p.Gly131Ala)
ClinVar gnomAD v4
14g.28767671G>TCA389475001FOXG1c.392G>T (p.Gly131Val)
ClinVar gnomAD v4
14g.28767672_28767673delCA2624399060FOXG1c.393_394del (p.Gly132ArgfsTer?)
gnomAD v4
14g.28767672C>ACA486098133FOXG1c.393C>A (p.Gly131=)
14g.28767672C=CA2125999297FOXG1c.393C= (p.Gly131=)
14g.28767672C>GCA486098134FOXG1c.393C>G (p.Gly131=)
dbSNP
14g.28767672C>TCA486098135FOXG1c.393C>T (p.Gly131=)
dbSNP gnomAD v4
14g.28767673G>ACA389475003FOXG1c.394G>A (p.Gly132Ser)
ClinVar dbSNP
14g.28767673G>CCA389475004FOXG1c.394G>C (p.Gly132Arg)
14g.28767673G=CA2125999303FOXG1c.394G= (p.Gly132=)
14g.28767673G>TCA389475005FOXG1c.394G>T (p.Gly132Cys)
dbSNP gnomAD v4
14g.28767674G>ACA389475006FOXG1c.395G>A (p.Gly132Asp)
14g.28767674G>CCA389475007FOXG1c.395G>C (p.Gly132Ala)
14g.28767674G>TCA389475008FOXG1c.395G>T (p.Gly132Val)
14g.28767675C>ACA486098136FOXG1c.396C>A (p.Gly132=)
gnomAD v4
14g.28767675C>GCA486098137FOXG1c.396C>G (p.Gly132=)
14g.28767675C>TCA486098139FOXG1c.396C>T (p.Gly132=)
gnomAD v4
14g.28767675_28767676delinsCGCA2125999307FOXG1c.396_397delinsCG (p.Gly132=)
14g.28767676G>ACA389475009FOXG1c.397G>A (p.Gly133Arg)
14g.28767676G>CCA389475010FOXG1c.397G>C (p.Gly133Arg)
ClinVar dbSNP gnomAD v4
14g.28767676G>TCA389475011FOXG1c.397G>T (p.Gly133Trp)
14g.28767678delCA314641FOXG1c.399del (p.Pro134ArgfsTer?)
ClinVar dbSNP gnomAD v4
14g.28767677G>ACA389475013FOXG1c.398G>A (p.Gly133Glu)
ClinVar
14g.28767677G>CCA389475014FOXG1c.398G>C (p.Gly133Ala)
14g.28767677G>TCA389475012FOXG1c.398G>T (p.Gly133Val)
14g.28767677_28767729delinsGGCCGGGGGAGCTGGCGCCCGTCGGGCCGGACGAGAAGGAGAAGGGCGCCGGCCA2125999315FOXG1c.398_450delinsGGCCGGGGGAGCTGGCGCCCGTCGGGCCGGACGAGAAGGAGAAGGGCGCCGGC (p.Gly133=)
14g.28767678G>ACA486098142FOXG1c.399G>A (p.Gly133=)
14g.28767678G>CCA486098143FOXG1c.399G>C (p.Gly133=)
14g.28767678G>TCA486098144FOXG1c.399G>T (p.Gly133=)
14g.28767686_28767737delCA891844335FOXG1c.407_458del (p.Glu136GlyfsTer?)
ClinVar dbSNP
14g.28767679C>ACA389475015FOXG1c.400C>A (p.Pro134Thr)
14g.28767679C=CA2125999320FOXG1c.400C= (p.Pro134=)
14g.28767679C>GCA389475016FOXG1c.400C>G (p.Pro134Ala)
14g.28767679C>TCA389475017FOXG1c.400C>T (p.Pro134Ser)
ClinVar dbSNP gnomAD v4
14g.28767680C>ACA389475018FOXG1c.401C>A (p.Pro134Gln)
gnomAD v4
14g.28767680C>GCA389475019FOXG1c.401C>G (p.Pro134Arg)
ClinVar dbSNP gnomAD v4
14g.28767680C>TCA389475020FOXG1c.401C>T (p.Pro134Leu)
gnomAD v4
14g.28767680_28767681delinsCGCA2125999325FOXG1c.401_402delinsCG (p.Pro134=)
14g.28767681G>ACA486098150FOXG1c.402G>A (p.Pro134=)
ClinVar dbSNP gnomAD v2 gnomAD v4
14g.28767681G>CCA486098148FOXG1c.402G>C (p.Pro134=)
dbSNP
14g.28767681G=CA2125999331FOXG1c.402G= (p.Pro134=)
14g.28767681G>TCA486098149FOXG1c.402G>T (p.Pro134=)
14g.28767685delCA1139663425FOXG1c.406del (p.Glu136SerfsTer?)
ClinVar dbSNP gnomAD v4
14g.28767682G>ACA389475021FOXG1c.403G>A (p.Gly135Arg)
dbSNP gnomAD v4
14g.28767682G>CCA389475022FOXG1c.403G>C (p.Gly135Arg)
14g.28767682G=CA2125999335FOXG1c.403G= (p.Gly135=)
14g.28767682G>TCA389475023FOXG1c.403G>T (p.Gly135Trp)
14g.28767683G>ACA389475024FOXG1c.404G>A (p.Gly135Glu)
dbSNP
14g.28767683G>CCA389475025FOXG1c.404G>C (p.Gly135Ala)
14g.28767683G=CA2125999339FOXG1c.404G= (p.Gly135=)
14g.28767683G>TCA389475026FOXG1c.404G>T (p.Gly135Val)
ClinVar dbSNP gnomAD v3 gnomAD v4
14g.28767684G>ACA486098156FOXG1c.405G>A (p.Gly135=)
ClinVar dbSNP
14g.28767684G>CCA486098155FOXG1c.405G>C (p.Gly135=)
dbSNP gnomAD v4
14g.28767684G=CA2125999342FOXG1c.405G= (p.Gly135=)
14g.28767684G>TCA486098154FOXG1c.405G>T (p.Gly135=)
gnomAD v4
14g.28767685G>ACA389475028FOXG1c.406G>A (p.Glu136Lys)
gnomAD v4
14g.28767685G>CCA389475027FOXG1c.406G>C (p.Glu136Gln)
14g.28767685G=CA2125999349FOXG1c.406G= (p.Glu136=)
14g.28767685G>TCA16606550FOXG1c.406G>T (p.Glu136Ter)
ClinVar dbSNP
14g.28767688_28767711delCA2580088000FOXG1c.409_432del (p.Leu137_Glu144del)
ClinVar
14g.28767687_28767748delCA2832528760FOXG1c.408_469del (p.Leu137GlyfsTer?)
14g.28767686A>CCA389475029FOXG1c.407A>C (p.Glu136Ala)
14g.28767686A>GCA389475030FOXG1c.407A>G (p.Glu136Gly)
14g.28767686A>TCA389475031FOXG1c.407A>T (p.Glu136Val)
14g.28767687G>ACA486098157FOXG1c.408G>A (p.Glu136=)
gnomAD v4
14g.28767687G>CCA389475032FOXG1c.408G>C (p.Glu136Asp)
14g.28767687G>TCA389475033FOXG1c.408G>T (p.Glu136Asp)
14g.28767688C>ACA389475034FOXG1c.409C>A (p.Leu137Met)
14g.28767688C=CA2125999352FOXG1c.409C= (p.Leu137=)
14g.28767688C>GCA389475035FOXG1c.409C>G (p.Leu137Val)
14g.28767688C>TCA486098159FOXG1c.409C>T (p.Leu137=)
dbSNP gnomAD v2 gnomAD v4
14g.28767689T>ACA389475036FOXG1c.410T>A (p.Leu137Gln)
14g.28767689T>CCA389475037FOXG1c.410T>C (p.Leu137Pro)
14g.28767689T>GCA389475038FOXG1c.410T>G (p.Leu137Arg)
14g.28767690G>ACA7140597FOXG1c.411G>A (p.Leu137=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.28767690G>CCA7140596FOXG1c.411G>C (p.Leu137=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.28767690G=CA2125999354FOXG1c.411G= (p.Leu137=)
14g.28767690G>TCA486098160FOXG1c.411G>T (p.Leu137=)
14g.28767691G>ACA389475041FOXG1c.412G>A (p.Ala138Thr)
ClinVar dbSNP gnomAD v3 gnomAD v4
14g.28767691G>CCA389475040FOXG1c.412G>C (p.Ala138Pro)
dbSNP gnomAD v3 gnomAD v4
14g.28767691G=CA2125999358FOXG1c.412G= (p.Ala138=)
14g.28767691G>TCA389475039FOXG1c.412G>T (p.Ala138Ser)
14g.28767692delCA2697553884FOXG1c.413del (p.Ala138GlyfsTer?)
ClinVar
14g.28767692C>ACA389475042FOXG1c.413C>A (p.Ala138Glu)
14g.28767692C>GCA389475043FOXG1c.413C>G (p.Ala138Gly)
COSMIC
14g.28767692C>TCA389475044FOXG1c.413C>T (p.Ala138Val)
ClinVar gnomAD v4
14g.28767693G>ACA486098162FOXG1c.414G>A (p.Ala138=)
14g.28767693G>CCA486098163FOXG1c.414G>C (p.Ala138=)
gnomAD v4
14g.28767693G=CA2125999361FOXG1c.414G= (p.Ala138=)
14g.28767693G>TCA258396567FOXG1c.414G>T (p.Ala138=)
ClinVar dbSNP gnomAD v2 gnomAD v4
14g.28767694C>ACA389475045FOXG1c.415C>A (p.Pro139Thr)
14g.28767694C=CA2125999363FOXG1c.415C= (p.Pro139=)
14g.28767694C>GCA389475046FOXG1c.415C>G (p.Pro139Ala)
14g.28767694C>TCA389475047FOXG1c.415C>T (p.Pro139Ser)
ClinVar dbSNP gnomAD v2 gnomAD v4
14g.28767695C>ACA389475050FOXG1c.416C>A (p.Pro139His)
14g.28767695C=CA2125999365FOXG1c.416C= (p.Pro139=)
14g.28767695C>GCA389475049FOXG1c.416C>G (p.Pro139Arg)
gnomAD v4
14g.28767695C>TCA389475048FOXG1c.416C>T (p.Pro139Leu)
dbSNP gnomAD v4
14g.28767696C>ACA486098164FOXG1c.417C>A (p.Pro139=)
dbSNP gnomAD v4
14g.28767696C=CA2125999368FOXG1c.417C= (p.Pro139=)
14g.28767696C>GCA486098165FOXG1c.417C>G (p.Pro139=)
ClinVar
14g.28767696C>TCA258396568FOXG1c.417C>T (p.Pro139=)
ClinVar dbSNP gnomAD v4
14g.28767697G>ACA389475051FOXG1c.418G>A (p.Val140Ile)
ClinVar dbSNP gnomAD v2 gnomAD v4
14g.28767697G>CCA389475052FOXG1c.418G>C (p.Val140Leu)
14g.28767697G=CA2125999371FOXG1c.418G= (p.Val140=)
14g.28767697G>TCA389475053FOXG1c.418G>T (p.Val140Phe)
14g.28767698T>ACA389475054FOXG1c.419T>A (p.Val140Asp)
dbSNP
14g.28767698T>CCA389475055FOXG1c.419T>C (p.Val140Ala)
14g.28767698T>GCA389475056FOXG1c.419T>G (p.Val140Gly)
14g.28767698T=CA2125999375FOXG1c.419T= (p.Val140=)
14g.28767699C>ACA16607633FOXG1c.420C>A (p.Val140=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.28767699C=CA2125999380FOXG1c.420C= (p.Val140=)
14g.28767699C>GCA486098167FOXG1c.420C>G (p.Val140=)
14g.28767699C>TCA16606973FOXG1c.420C>T (p.Val140=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.28767700G>ACA389475057FOXG1c.421G>A (p.Gly141Arg)
ClinVar dbSNP gnomAD v4
14g.28767700G>CCA389475059FOXG1c.421G>C (p.Gly141Arg)
dbSNP gnomAD v4
14g.28767700G=CA2125999384FOXG1c.421G= (p.Gly141=)
14g.28767700G>TCA389475058FOXG1c.421G>T (p.Gly141Trp)
gnomAD v4
14g.28767701G>ACA389475060FOXG1c.422G>A (p.Gly141Glu)
14g.28767701G>CCA389475061FOXG1c.422G>C (p.Gly141Ala)
14g.28767701G>TCA389475062FOXG1c.422G>T (p.Gly141Val)
ClinVar gnomAD v4
14g.28767702G>ACA486098169FOXG1c.423G>A (p.Gly141=)
gnomAD v4
14g.28767702G>CCA486098171FOXG1c.423G>C (p.Gly141=)
14g.28767702G>TCA486098170FOXG1c.423G>T (p.Gly141=)
ClinVar
14g.28767703C>ACA389475063FOXG1c.424C>A (p.Pro142Thr)
gnomAD v4
14g.28767703C>GCA389475064FOXG1c.424C>G (p.Pro142Ala)
ClinVar
14g.28767703C>TCA389475065FOXG1c.424C>T (p.Pro142Ser)
ClinVar dbSNP gnomAD v4
14g.28767704C>ACA389475066FOXG1c.425C>A (p.Pro142Gln)
gnomAD v4
14g.28767704C>GCA389475067FOXG1c.425C>G (p.Pro142Arg)
gnomAD v4
14g.28767704C>TCA389475068FOXG1c.425C>T (p.Pro142Leu)
gnomAD v4
14g.28767705G>ACA486098172FOXG1c.426G>A (p.Pro142=)
dbSNP gnomAD v4
14g.28767705G>CCA486098173FOXG1c.426G>C (p.Pro142=)
14g.28767705G=CA2125999388FOXG1c.426G= (p.Pro142=)
14g.28767705G>TCA486098175FOXG1c.426G>T (p.Pro142=)
ClinVar
14g.28767706G>ACA389475069FOXG1c.427G>A (p.Asp143Asn)
14g.28767706G>CCA389475070FOXG1c.427G>C (p.Asp143His)
14g.28767706G>TCA389475071FOXG1c.427G>T (p.Asp143Tyr)
14g.28767707A>CCA389475072FOXG1c.428A>C (p.Asp143Ala)
14g.28767707A>GCA389475074FOXG1c.428A>G (p.Asp143Gly)
gnomAD v4
14g.28767707A>TCA389475073FOXG1c.428A>T (p.Asp143Val)
14g.28767708C>ACA389475075FOXG1c.429C>A (p.Asp143Glu)
dbSNP gnomAD v2 gnomAD v4
14g.28767708C=CA2125999393FOXG1c.429C= (p.Asp143=)
14g.28767708C>GCA7140598FOXG1c.429C>G (p.Asp143Glu)
ClinVar dbSNP ExAC gnomAD v4
14g.28767708C>TCA486098178FOXG1c.429C>T (p.Asp143=)
dbSNP gnomAD v2 gnomAD v4
14g.28767709G>ACA206112FOXG1c.430G>A (p.Glu144Lys)
ClinVar dbSNP
14g.28767709G>CCA389475076FOXG1c.430G>C (p.Glu144Gln)
gnomAD v4
14g.28767709G=CA2125999403FOXG1c.430G= (p.Glu144=)
14g.28767709G>TCA389475077FOXG1c.430G>T (p.Glu144Ter)
ClinVar dbSNP
14g.28767709_28767712delinsGAGACA2125999406FOXG1c.430_433delinsGAGA (p.Glu144=)
14g.28767716_28767721dupCA915948873FOXG1c.437_442dup (p.Lys147_Gly148insGluLys)
ClinVar dbSNP
14g.28767710A>CCA389475078FOXG1c.431A>C (p.Glu144Ala)
14g.28767710A>GCA389475079FOXG1c.431A>G (p.Glu144Gly)
14g.28767710A>TCA389475080FOXG1c.431A>T (p.Glu144Val)
gnomAD v4
14g.28767712_28767714delCA613324872FOXG1c.433_435del (p.Lys145del)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.28767711G>ACA486098182FOXG1c.432G>A (p.Glu144=)
gnomAD v4
14g.28767711G>CCA314586FOXG1c.432G>C (p.Glu144Asp)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.28767711G=CA2125999411FOXG1c.432G= (p.Glu144=)
14g.28767711G>TCA389475081FOXG1c.432G>T (p.Glu144Asp)
14g.28767712A=CA2125999416FOXG1c.433A= (p.Lys145=)
14g.28767712A>CCA389475082FOXG1c.433A>C (p.Lys145Gln)
14g.28767712A>GCA389475083FOXG1c.433A>G (p.Lys145Glu)
dbSNP gnomAD v3 gnomAD v4
14g.28767712A>TCA389475084FOXG1c.433A>T (p.Lys145Ter)
14g.28767712_28767715delinsAAGGCA2125999415FOXG1c.433_436delinsAAGG (p.Lys145=)
14g.28767713A=CA2125999419FOXG1c.434A= (p.Lys145=)
14g.28767713A>CCA389475087FOXG1c.434A>C (p.Lys145Thr)
dbSNP gnomAD v3 gnomAD v4
14g.28767713A>GCA389475085FOXG1c.434A>G (p.Lys145Arg)
gnomAD v4
14g.28767713A>TCA389475086FOXG1c.434A>T (p.Lys145Met)
14g.28767715_28767717delCA7140599FOXG1c.436_438del (p.Glu146del)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.28767714G>ACA486098183FOXG1c.435G>A (p.Lys145=)
dbSNP gnomAD v2 gnomAD v4
14g.28767714G>CCA389475088FOXG1c.435G>C (p.Lys145Asn)
14g.28767714G=CA2125999421FOXG1c.435G= (p.Lys145=)
14g.28767714G>TCA389475089FOXG1c.435G>T (p.Lys145Asn)
COSMIC
14g.28767714_28767715delCA2739291836FOXG1c.435_436del (p.Lys147GlyfsTer?)
14g.28767715G>ACA389475090FOXG1c.436G>A (p.Glu146Lys)
14g.28767715G>CCA389475091FOXG1c.436G>C (p.Glu146Gln)
dbSNP gnomAD v4
14g.28767715G=CA2125999424FOXG1c.436G= (p.Glu146=)
14g.28767715G>TCA389475092FOXG1c.436G>T (p.Glu146Ter)
ClinVar dbSNP
14g.28767716A=CA2125999432FOXG1c.437A= (p.Glu146=)
14g.28767716A>CCA389475093FOXG1c.437A>C (p.Glu146Ala)
gnomAD v4
14g.28767716A>GCA16607634FOXG1c.437A>G (p.Glu146Gly)
ClinVar dbSNP
14g.28767716A>TCA258396569FOXG1c.437A>T (p.Glu146Val)
dbSNP
14g.28767717G>ACA258396570FOXG1c.438G>A (p.Glu146=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.28767717G>CCA389475094FOXG1c.438G>C (p.Glu146Asp)
gnomAD v4
14g.28767717G=CA2125999436FOXG1c.438G= (p.Glu146=)
14g.28767717G>TCA389475095FOXG1c.438G>T (p.Glu146Asp)
14g.28767718A>CCA389475096FOXG1c.439A>C (p.Lys147Gln)
14g.28767718A>GCA389475098FOXG1c.439A>G (p.Lys147Glu)
14g.28767718A>TCA389475097FOXG1c.439A>T (p.Lys147Ter)
ClinVar
14g.28767719A=CA2125999440FOXG1c.440A= (p.Lys147=)
14g.28767719A>CCA389475099FOXG1c.440A>C (p.Lys147Thr)
14g.28767719A>GCA389475101FOXG1c.440A>G (p.Lys147Arg)
ClinVar dbSNP
14g.28767719A>TCA389475100FOXG1c.440A>T (p.Lys147Met)
ClinVar dbSNP
14g.28767720G>ACA486098186FOXG1c.441G>A (p.Lys147=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.28767720G>CCA389475102FOXG1c.441G>C (p.Lys147Asn)
14g.28767720G=CA2125999442FOXG1c.441G= (p.Lys147=)
14g.28767720G>TCA389475103FOXG1c.441G>T (p.Lys147Asn)
gnomAD v4
14g.28767721G>ACA389475104FOXG1c.442G>A (p.Gly148Ser)
14g.28767721G>CCA389475105FOXG1c.442G>C (p.Gly148Arg)
14g.28767721G=CA2125999446FOXG1c.442G= (p.Gly148=)
14g.28767721G>TCA389475106FOXG1c.442G>T (p.Gly148Cys)
dbSNP gnomAD v2
14g.28767729_28767734dupCA7140600FOXG1c.450_455dup (p.Gly152_Gly153insAlaGly)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.28767722G>ACA389475107FOXG1c.443G>A (p.Gly148Asp)
ClinVar dbSNP gnomAD v2 gnomAD v4
14g.28767722G>CCA389475108FOXG1c.443G>C (p.Gly148Ala)
ClinVar
14g.28767722G=CA2125999448FOXG1c.443G= (p.Gly148=)
14g.28767722G>TCA7140601FOXG1c.443G>T (p.Gly148Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched