Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.28768103G>ACA389475947FOXG1c.824G>A (p.Arg275His)
dbSNP
14g.28768103G>CCA389475948FOXG1c.824G>C (p.Arg275Pro)
ClinVar dbSNP
14g.28768103G=CA2126000282FOXG1c.824G= (p.Arg275=)
14g.28768103G>TCA389475949FOXG1c.824G>T (p.Arg275Leu)
14g.28768104C>ACA486099016FOXG1c.825C>A (p.Arg275=)
14g.28768104C>GCA486099015FOXG1c.825C>G (p.Arg275=)
14g.28768104C>TCA486099014FOXG1c.825C>T (p.Arg275=)
gnomAD v4 COSMIC
14g.28768105C>ACA389475951FOXG1c.826C>A (p.Arg276Ser)
14g.28768105C>GCA389475952FOXG1c.826C>G (p.Arg276Gly)
14g.28768105C>TCA389475950FOXG1c.826C>T (p.Arg276Cys)
ClinVar dbSNP
14g.28768106G>ACA389475955FOXG1c.827G>A (p.Arg276His)
dbSNP gnomAD v2 gnomAD v4
14g.28768106G>CCA389475953FOXG1c.827G>C (p.Arg276Pro)
14g.28768106G=CA2126000283FOXG1c.827G= (p.Arg276=)
14g.28768106G>TCA389475954FOXG1c.827G>T (p.Arg276Leu)
gnomAD v4
14g.28768107C>ACA486099025FOXG1c.828C>A (p.Arg276=)
14g.28768107C=CA2126000284FOXG1c.828C= (p.Arg276=)
14g.28768107C>GCA486099024FOXG1c.828C>G (p.Arg276=)
14g.28768107C>TCA486099022FOXG1c.828C>T (p.Arg276=)
dbSNP gnomAD v2 gnomAD v4
14g.28768108T>ACA389475956FOXG1c.829T>A (p.Ser277Thr)
14g.28768108T>CCA389475957FOXG1c.829T>C (p.Ser277Pro)
14g.28768108T>GCA389475958FOXG1c.829T>G (p.Ser277Ala)
14g.28768109C>ACA389475959FOXG1c.830C>A (p.Ser277Tyr)
14g.28768109C>GCA389475960FOXG1c.830C>G (p.Ser277Cys)
14g.28768109C>TCA389475961FOXG1c.830C>T (p.Ser277Phe)
14g.28768110C>ACA486099033FOXG1c.831C>A (p.Ser277=)
14g.28768110C>GCA486099035FOXG1c.831C>G (p.Ser277=)
14g.28768110C>TCA486099034FOXG1c.831C>T (p.Ser277=)
14g.28768111A>CCA389475962FOXG1c.832A>C (p.Thr278Pro)
14g.28768111A>GCA389475963FOXG1c.832A>G (p.Thr278Ala)
COSMIC
14g.28768111A>TCA389475964FOXG1c.832A>T (p.Thr278Ser)
14g.28768112C>ACA389475965FOXG1c.833C>A (p.Thr278Asn)
14g.28768112C>GCA389475966FOXG1c.833C>G (p.Thr278Ser)
14g.28768112C>TCA389475967FOXG1c.833C>T (p.Thr278Ile)
gnomAD v4
14g.28768113C>ACA486099042FOXG1c.834C>A (p.Thr278=)
14g.28768113C=CA2126000285FOXG1c.834C= (p.Thr278=)
14g.28768113C>GCA486099043FOXG1c.834C>G (p.Thr278=)
14g.28768113C>TCA7140632FOXG1c.834C>T (p.Thr278=)
dbSNP ExAC gnomAD v2 gnomAD v4
14g.28768114A>CCA389475968FOXG1c.835A>C (p.Thr279Pro)
14g.28768114A>GCA389475969FOXG1c.835A>G (p.Thr279Ala)
14g.28768114A>TCA389475970FOXG1c.835A>T (p.Thr279Ser)
14g.28768115C>ACA389475971FOXG1c.836C>A (p.Thr279Asn)
ClinVar gnomAD v4 COSMIC
14g.28768115C>GCA389475972FOXG1c.836C>G (p.Thr279Ser)
14g.28768115C>TCA389475973FOXG1c.836C>T (p.Thr279Ile)
14g.28768116C>ACA486099049FOXG1c.837C>A (p.Thr279=)
14g.28768116C=CA2126000286FOXG1c.837C= (p.Thr279=)
14g.28768116C>GCA486099051FOXG1c.837C>G (p.Thr279=)
ClinVar dbSNP gnomAD v2 gnomAD v4
14g.28768116C>TCA7140633FOXG1c.837C>T (p.Thr279=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
14g.28768117T>ACA389475974FOXG1c.838T>A (p.Ser280Thr)
14g.28768117T>CCA389475975FOXG1c.838T>C (p.Ser280Pro)
14g.28768117T>GCA389475976FOXG1c.838T>G (p.Ser280Ala)

Number of alleles fetched