Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.28767412_28767748delinsACCCACCGCCCCCA2766230034FOXG1c.133_469delinsACCCACCGCCCC (p.Pro45ThrfsTer?)
14g.28767634_28767648delCA2624398994FOXG1c.355_369del (p.Ala119_Gly123del)
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

Number of alleles fetched