Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.28768117T>ACA389475974FOXG1c.838T>A (p.Ser280Thr)
14g.28768117T>CCA389475975FOXG1c.838T>C (p.Ser280Pro)
14g.28768117T>GCA389475976FOXG1c.838T>G (p.Ser280Ala)
14g.28768118C>ACA389475977FOXG1c.839C>A (p.Ser280Ter)
COSMIC
14g.28768118C=CA2126000287FOXG1c.839C= (p.Ser280=)
14g.28768118C>GCA389475978FOXG1c.839C>G (p.Ser280Trp)
gnomAD v4
14g.28768118C>TCA258396581FOXG1c.839C>T (p.Ser280Leu)
dbSNP
14g.28768119G>ACA486099056FOXG1c.840G>A (p.Ser280=)
gnomAD v4
14g.28768119G>CCA486099057FOXG1c.840G>C (p.Ser280=)
14g.28768119G=CA2126000288FOXG1c.840G= (p.Ser280=)
14g.28768119G>TCA486099058FOXG1c.840G>T (p.Ser280=)
dbSNP gnomAD v2 gnomAD v4
14g.28768120delCA2580088020FOXG1c.841del (p.Arg281GlyfsTer?)
ClinVar
14g.28768120C>ACA486099062FOXG1c.841C>A (p.Arg281=)
14g.28768120C>GCA389475980FOXG1c.841C>G (p.Arg281Gly)
14g.28768120C>TCA389475979FOXG1c.841C>T (p.Arg281Trp)
COSMIC
14g.28768121G>ACA389475981FOXG1c.842G>A (p.Arg281Gln)
14g.28768121G>CCA389475982FOXG1c.842G>C (p.Arg281Pro)
dbSNP COSMIC
14g.28768121G=CA2126000289FOXG1c.842G= (p.Arg281=)
14g.28768121G>TCA389475983FOXG1c.842G>T (p.Arg281Leu)
14g.28768123dupCA2573053898FOXG1c.844dup (p.Ala282GlyfsTer?)
ClinVar dbSNP
14g.28768122G>ACA7140634FOXG1c.843G>A (p.Arg281=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.28768122G>CCA486099066FOXG1c.843G>C (p.Arg281=)
14g.28768122G=CA2126000290FOXG1c.843G= (p.Arg281=)
14g.28768122G>TCA486099067FOXG1c.843G>T (p.Arg281=)
COSMIC
14g.28768123G>ACA314626FOXG1c.844G>A (p.Ala282Thr)
ClinVar dbSNP gnomAD v4
14g.28768123G>CCA389475984FOXG1c.844G>C (p.Ala282Pro)
14g.28768123G=CA2126000291FOXG1c.844G= (p.Ala282=)
14g.28768123G>TCA389475985FOXG1c.844G>T (p.Ala282Ser)
dbSNP gnomAD v2 gnomAD v4
14g.28768124C>ACA389475986FOXG1c.845C>A (p.Ala282Asp)
14g.28768124C>GCA389475987FOXG1c.845C>G (p.Ala282Gly)
14g.28768124C>TCA389475988FOXG1c.845C>T (p.Ala282Val)
COSMIC
14g.28768125C>ACA486099070FOXG1c.846C>A (p.Ala282=)
gnomAD v4
14g.28768125C>GCA486099071FOXG1c.846C>G (p.Ala282=)
14g.28768125C>TCA486099069FOXG1c.846C>T (p.Ala282=)
14g.28768126A>CCA389475989FOXG1c.847A>C (p.Lys283Gln)
14g.28768126A>GCA389475990FOXG1c.847A>G (p.Lys283Glu)
14g.28768126A>TCA389475991FOXG1c.847A>T (p.Lys283Ter)
ClinVar
14g.28768126_28768127insGACCCA961450741FOXG1c.847_848insGACC (p.Lys283ArgfsTer?)
gnomAD v3 gnomAD v4
14g.28768127A>CCA389475993FOXG1c.848A>C (p.Lys283Thr)
14g.28768127A>GCA389475994FOXG1c.848A>G (p.Lys283Arg)
COSMIC
14g.28768127A>TCA389475992FOXG1c.848A>T (p.Lys283Met)
14g.28768128G>ACA486099072FOXG1c.849G>A (p.Lys283=)
ClinVar dbSNP gnomAD v3 gnomAD v4
14g.28768128G>CCA389475995FOXG1c.849G>C (p.Lys283Asn)
14g.28768128G=CA2126000292FOXG1c.849G= (p.Lys283=)
14g.28768128G>TCA389475996FOXG1c.849G>T (p.Lys283Asn)
14g.28768129C>ACA389475997FOXG1c.850C>A (p.Leu284Met)
14g.28768129C=CA2126000293FOXG1c.850C= (p.Leu284=)
14g.28768129C>GCA389475998FOXG1c.850C>G (p.Leu284Val)
14g.28768129C>TCA258396582FOXG1c.850C>T (p.Leu284=)
dbSNP gnomAD v4
14g.28768130T>ACA389475999FOXG1c.851T>A (p.Leu284Gln)

Number of alleles fetched