Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.28768072_28768087delCA2573149903FOXG1c.793_808del (p.Phe265ArgfsTer?)
ClinVar dbSNP
14g.28768081_28768083delCA2739277845FOXG1c.802_804del (p.Gly268del)
ClinVar
14g.28768078G>ACA172199FOXG1c.799G>A (p.Gly267Ser)
ClinVar dbSNP
14g.28768078G>CCA389475899FOXG1c.799G>C (p.Gly267Arg)
14g.28768078G=CA2126000267FOXG1c.799G= (p.Gly267=)
14g.28768078G>TCA389475900FOXG1c.799G>T (p.Gly267Cys)
14g.28768079G>ACA389475901FOXG1c.800G>A (p.Gly267Asp)
ClinVar
14g.28768079G>CCA389475902FOXG1c.800G>C (p.Gly267Ala)
14g.28768079G>TCA389475903FOXG1c.800G>T (p.Gly267Val)
14g.28768080C>ACA486098949FOXG1c.801C>A (p.Gly267=)
ClinVar dbSNP gnomAD v2 gnomAD v4
14g.28768080C=CA2126000272FOXG1c.801C= (p.Gly267=)
14g.28768080C>GCA486098950FOXG1c.801C>G (p.Gly267=)
14g.28768080C>TCA486098951FOXG1c.801C>T (p.Gly267=)
14g.28768081G>ACA389475904FOXG1c.802G>A (p.Gly268Ser)
COSMIC
14g.28768081G>CCA389475905FOXG1c.802G>C (p.Gly268Arg)
COSMIC
14g.28768081G>TCA389475906FOXG1c.802G>T (p.Gly268Cys)
14g.28768082delCA2586963983FOXG1c.803del (p.Gly268AlafsTer?)
ClinVar
14g.28768082G>ACA389475907FOXG1c.803G>A (p.Gly268Asp)
14g.28768082G>CCA389475908FOXG1c.803G>C (p.Gly268Ala)
14g.28768082G>TCA389475909FOXG1c.803G>T (p.Gly268Val)
ClinVar dbSNP gnomAD v4
14g.28768083C>ACA486098955FOXG1c.804C>A (p.Gly268=)
gnomAD v4
14g.28768083C>GCA486098957FOXG1c.804C>G (p.Gly268=)
14g.28768083C>TCA486098956FOXG1c.804C>T (p.Gly268=)
ClinVar
14g.28768084A>CCA389475912FOXG1c.805A>C (p.Thr269Pro)
gnomAD v4
14g.28768084A>GCA389475910FOXG1c.805A>G (p.Thr269Ala)
14g.28768084A>TCA389475911FOXG1c.805A>T (p.Thr269Ser)
14g.28768085C>ACA389475913FOXG1c.806C>A (p.Thr269Asn)
14g.28768085C>GCA389475914FOXG1c.806C>G (p.Thr269Ser)
14g.28768085C>TCA389475915FOXG1c.806C>T (p.Thr269Ile)
14g.28768086C>ACA486098967FOXG1c.807C>A (p.Thr269=)
14g.28768086C>GCA486098968FOXG1c.807C>G (p.Thr269=)
14g.28768086C>TCA486098969FOXG1c.807C>T (p.Thr269=)
gnomAD v4
14g.28768087A=CA2126000273FOXG1c.808A= (p.Thr270=)
14g.28768087A>CCA389475916FOXG1c.808A>C (p.Thr270Pro)
14g.28768087A>GCA389475917FOXG1c.808A>G (p.Thr270Ala)
dbSNP gnomAD v2 gnomAD v4
14g.28768087A>TCA389475918FOXG1c.808A>T (p.Thr270Ser)
14g.28768088C>ACA389475919FOXG1c.809C>A (p.Thr270Lys)
COSMIC
14g.28768088C>GCA389475920FOXG1c.809C>G (p.Thr270Arg)
14g.28768088C>TCA389475921FOXG1c.809C>T (p.Thr270Met)
gnomAD v4 COSMIC
14g.28768089G>ACA7140631FOXG1c.810G>A (p.Thr270=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.28768089G>CCA486098973FOXG1c.810G>C (p.Thr270=)
ClinVar gnomAD v4
14g.28768089G=CA2126000274FOXG1c.810G= (p.Thr270=)
14g.28768089G>TCA486098975FOXG1c.810G>T (p.Thr270=)
gnomAD v4
14g.28768090G>ACA389475924FOXG1c.811G>A (p.Gly271Ser)
ClinVar dbSNP
14g.28768090G>CCA389475923FOXG1c.811G>C (p.Gly271Arg)
14g.28768090G=CA2126000275FOXG1c.811G= (p.Gly271=)
14g.28768090G>TCA389475922FOXG1c.811G>T (p.Gly271Cys)
ClinVar
14g.28768091G>ACA314624FOXG1c.812G>A (p.Gly271Asp)
ClinVar dbSNP COSMIC
14g.28768091G>CCA389475925FOXG1c.812G>C (p.Gly271Ala)
14g.28768091G=CA2126000276FOXG1c.812G= (p.Gly271=)
14g.28768091G>TCA389475926FOXG1c.812G>T (p.Gly271Val)
14g.28768092C>ACA486098981FOXG1c.813C>A (p.Gly271=)
14g.28768092C=CA2126000277FOXG1c.813C= (p.Gly271=)
14g.28768092C>GCA486098982FOXG1c.813C>G (p.Gly271=)
14g.28768092C>TCA486098983FOXG1c.813C>T (p.Gly271=)
dbSNP gnomAD v4
14g.28768093A>CCA389475927FOXG1c.814A>C (p.Lys272Gln)
14g.28768093A>GCA389475928FOXG1c.814A>G (p.Lys272Glu)
14g.28768093A>TCA389475929FOXG1c.814A>T (p.Lys272Ter)
14g.28768093_28768100delCA2573332464FOXG1c.814_821del (p.Lys272AlafsTer?)
ClinVar
14g.28768094A>CCA389475930FOXG1c.815A>C (p.Lys272Thr)
14g.28768094A>GCA389475931FOXG1c.815A>G (p.Lys272Arg)
14g.28768094A>TCA389475932FOXG1c.815A>T (p.Lys272Met)
14g.28768095G>ACA486098988FOXG1c.816G>A (p.Lys272=)
14g.28768095G>CCA389475933FOXG1c.816G>C (p.Lys272Asn)
14g.28768095G>TCA389475934FOXG1c.816G>T (p.Lys272Asn)
gnomAD v4
14g.28768096C>ACA389475935FOXG1c.817C>A (p.Leu273Met)
gnomAD v4
14g.28768096C>GCA389475936FOXG1c.817C>G (p.Leu273Val)
14g.28768096C>TCA486098991FOXG1c.817C>T (p.Leu273=)
ClinVar
14g.28768097T>ACA389475937FOXG1c.818T>A (p.Leu273Gln)
14g.28768097T>CCA389475939FOXG1c.818T>C (p.Leu273Pro)
14g.28768097T>GCA389475938FOXG1c.818T>G (p.Leu273Arg)
14g.28768098G>ACA486098997FOXG1c.819G>A (p.Leu273=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.28768098G>CCA486098998FOXG1c.819G>C (p.Leu273=)
14g.28768098G=CA2126000278FOXG1c.819G= (p.Leu273=)
14g.28768098G>TCA486099001FOXG1c.819G>T (p.Leu273=)
gnomAD v4
14g.28768099C>ACA486099003FOXG1c.820C>A (p.Arg274=)
dbSNP gnomAD v2 gnomAD v4
14g.28768099C=CA2126000279FOXG1c.820C= (p.Arg274=)
14g.28768099C>GCA389475940FOXG1c.820C>G (p.Arg274Gly)
14g.28768099C>TCA389475941FOXG1c.820C>T (p.Arg274Trp)
gnomAD v4 COSMIC
14g.28768100G>ACA357167FOXG1c.821G>A (p.Arg274Gln)
ClinVar dbSNP
14g.28768100G>CCA389475942FOXG1c.821G>C (p.Arg274Pro)
ClinVar dbSNP
14g.28768100G=CA2126000280FOXG1c.821G= (p.Arg274=)
14g.28768100G>TCA389475943FOXG1c.821G>T (p.Arg274Leu)
14g.28768101G>ACA486099007FOXG1c.822G>A (p.Arg274=)
dbSNP gnomAD v3 gnomAD v4
14g.28768101G>CCA486099008FOXG1c.822G>C (p.Arg274=)
14g.28768101G=CA2126000281FOXG1c.822G= (p.Arg274=)
14g.28768101G>TCA486099009FOXG1c.822G>T (p.Arg274=)
COSMIC
14g.28768102C>ACA389475944FOXG1c.823C>A (p.Arg275Ser)
14g.28768102C>GCA389475945FOXG1c.823C>G (p.Arg275Gly)
14g.28768102C>TCA389475946FOXG1c.823C>T (p.Arg275Cys)
COSMIC
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)
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)
14g.28768130T>CCA389476000FOXG1c.851T>C (p.Leu284Pro)
14g.28768130T>GCA389476001FOXG1c.851T>G (p.Leu284Arg)
14g.28768131G>ACA7140635FOXG1c.852G>A (p.Leu284=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.28768131G>CCA486099074FOXG1c.852G>C (p.Leu284=)
14g.28768131G=CA2126000294FOXG1c.852G= (p.Leu284=)
14g.28768131G>TCA486099073FOXG1c.852G>T (p.Leu284=)
gnomAD v4
14g.28768132G>ACA389476002FOXG1c.853G>A (p.Ala285Thr)
dbSNP
14g.28768132G>CCA389476003FOXG1c.853G>C (p.Ala285Pro)
14g.28768132G=CA2126000296FOXG1c.853G= (p.Ala285=)
14g.28768132G>TCA389476004FOXG1c.853G>T (p.Ala285Ser)
14g.28768132_28768133delinsGCCA2126000295FOXG1c.853_854delinsGC (p.Ala285=)
14g.28768133C>ACA389476005FOXG1c.854C>A (p.Ala285Asp)
14g.28768133C>GCA389476006FOXG1c.854C>G (p.Ala285Gly)
14g.28768133C>TCA389476007FOXG1c.854C>T (p.Ala285Val)
14g.28768134delCA658798197FOXG1c.855del (p.Phe286SerfsTer?)
ClinVar dbSNP
14g.28768134C>ACA486099075FOXG1c.855C>A (p.Ala285=)
gnomAD v4
14g.28768134C=CA2126000297FOXG1c.855C= (p.Ala285=)
14g.28768134C>GCA486099077FOXG1c.855C>G (p.Ala285=)
14g.28768134C>TCA486099076FOXG1c.855C>T (p.Ala285=)
dbSNP gnomAD v3 gnomAD v4
14g.28768135T>ACA389476010FOXG1c.856T>A (p.Phe286Ile)
14g.28768135T>CCA389476009FOXG1c.856T>C (p.Phe286Leu)
14g.28768135T>GCA389476008FOXG1c.856T>G (p.Phe286Val)
14g.28768136delCA2695219196FOXG1c.857del (p.Phe286SerfsTer?)
14g.28768136T>ACA389476011FOXG1c.857T>A (p.Phe286Tyr)
gnomAD v4
14g.28768136T>CCA389476013FOXG1c.857T>C (p.Phe286Ser)
14g.28768136T>GCA389476012FOXG1c.857T>G (p.Phe286Cys)
14g.28768137C>ACA7140636FOXG1c.858C>A (p.Phe286Leu)
dbSNP ExAC gnomAD v2 gnomAD v4
14g.28768137C=CA2126000298FOXG1c.858C= (p.Phe286=)
14g.28768137C>GCA389476014FOXG1c.858C>G (p.Phe286Leu)
14g.28768137C>TCA486099078FOXG1c.858C>T (p.Phe286=)
14g.28768137dupCA2695219197FOXG1c.858dup (p.Lys287GlnfsTer?)
14g.28768138A=CA2126000299FOXG1c.859A= (p.Lys287=)
14g.28768138A>CCA389476015FOXG1c.859A>C (p.Lys287Gln)
14g.28768138A>GCA389476017FOXG1c.859A>G (p.Lys287Glu)
14g.28768138A>TCA389476016FOXG1c.859A>T (p.Lys287Ter)
ClinVar dbSNP
14g.28768139A>CCA389476018FOXG1c.860A>C (p.Lys287Thr)
14g.28768139A>GCA389476019FOXG1c.860A>G (p.Lys287Arg)
14g.28768139A>TCA389476020FOXG1c.860A>T (p.Lys287Met)
14g.28768140G>ACA486099079FOXG1c.861G>A (p.Lys287=)
COSMIC
14g.28768140G>CCA389476021FOXG1c.861G>C (p.Lys287Asn)
14g.28768140G>TCA389476022FOXG1c.861G>T (p.Lys287Asn)
14g.28768141C>ACA389476023FOXG1c.862C>A (p.Arg288Ser)
dbSNP gnomAD v2 gnomAD v4
14g.28768141C=CA2126000300FOXG1c.862C= (p.Arg288=)
14g.28768141C>GCA389476024FOXG1c.862C>G (p.Arg288Gly)
14g.28768141C>TCA389476025FOXG1c.862C>T (p.Arg288Cys)
14g.28768142G>ACA389476026FOXG1c.863G>A (p.Arg288His)
COSMIC
14g.28768142G>CCA389476027FOXG1c.863G>C (p.Arg288Pro)
14g.28768142G>TCA389476028FOXG1c.863G>T (p.Arg288Leu)
14g.28768143C>ACA486099080FOXG1c.864C>A (p.Arg288=)
ClinVar
14g.28768143C=CA2126000301FOXG1c.864C= (p.Arg288=)
14g.28768143C>GCA486099081FOXG1c.864C>G (p.Arg288=)
ClinVar dbSNP
14g.28768143C>TCA486099082FOXG1c.864C>T (p.Arg288=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.28768144G>ACA389476031FOXG1c.865G>A (p.Gly289Ser)
COSMIC
14g.28768144G>CCA389476030FOXG1c.865G>C (p.Gly289Arg)
14g.28768144G>TCA389476029FOXG1c.865G>T (p.Gly289Cys)
gnomAD v4
14g.28768145G>ACA389476032FOXG1c.866G>A (p.Gly289Asp)
14g.28768145G>CCA389476033FOXG1c.866G>C (p.Gly289Ala)
14g.28768145G>TCA389476034FOXG1c.866G>T (p.Gly289Val)
14g.28768146T>ACA486099083FOXG1c.867T>A (p.Gly289=)
gnomAD v4
14g.28768146T>CCA486099084FOXG1c.867T>C (p.Gly289=)
14g.28768146T>GCA486099085FOXG1c.867T>G (p.Gly289=)
gnomAD v4
14g.28768147G>ACA389476035FOXG1c.868G>A (p.Ala290Thr)
COSMIC
14g.28768147G>CCA389476036FOXG1c.868G>C (p.Ala290Pro)
14g.28768147G>TCA389476037FOXG1c.868G>T (p.Ala290Ser)
gnomAD v4
14g.28768148C>ACA389476038FOXG1c.869C>A (p.Ala290Glu)
14g.28768148C>GCA389476039FOXG1c.869C>G (p.Ala290Gly)
14g.28768148C>TCA389476040FOXG1c.869C>T (p.Ala290Val)
ClinVar
14g.28768149G>ACA486099086FOXG1c.870G>A (p.Ala290=)
14g.28768149G>CCA486099088FOXG1c.870G>C (p.Ala290=)
COSMIC
14g.28768149G>TCA486099087FOXG1c.870G>T (p.Ala290=)
gnomAD v4
14g.28768150C>ACA389476041FOXG1c.871C>A (p.Arg291Ser)
14g.28768150C>GCA389476042FOXG1c.871C>G (p.Arg291Gly)
14g.28768150C>TCA389476043FOXG1c.871C>T (p.Arg291Cys)
14g.28768151G>ACA389476046FOXG1c.872G>A (p.Arg291His)
14g.28768151G>CCA389476045FOXG1c.872G>C (p.Arg291Pro)
14g.28768151G>TCA389476044FOXG1c.872G>T (p.Arg291Leu)
gnomAD v4
14g.28768160_28768174delCA2624399950FOXG1c.881_895del (p.Ser294_Thr298del)
gnomAD v4
14g.28768152C>ACA486099089FOXG1c.873C>A (p.Arg291=)
14g.28768152C>GCA486099090FOXG1c.873C>G (p.Arg291=)
14g.28768152C>TCA486099091FOXG1c.873C>T (p.Arg291=)
14g.28768153C>ACA389476047FOXG1c.874C>A (p.Leu292Ile)
14g.28768153C>GCA389476048FOXG1c.874C>G (p.Leu292Val)
gnomAD v4
14g.28768153C>TCA389476049FOXG1c.874C>T (p.Leu292Phe)
14g.28768154T>ACA389476050FOXG1c.875T>A (p.Leu292His)
COSMIC
14g.28768154T>CCA389476051FOXG1c.875T>C (p.Leu292Pro)
14g.28768154T>GCA389476052FOXG1c.875T>G (p.Leu292Arg)
14g.28768155C>ACA486098208FOXG1c.876C>A (p.Leu292=)
14g.28768155C=CA2126000302FOXG1c.876C= (p.Leu292=)
14g.28768155C>GCA486098210FOXG1c.876C>G (p.Leu292=)
ClinVar
14g.28768155C>TCA486098209FOXG1c.876C>T (p.Leu292=)
dbSNP gnomAD v2
14g.28768156A=CA2126000303FOXG1c.877A= (p.Thr293=)
14g.28768156A>CCA258396583FOXG1c.877A>C (p.Thr293Pro)
dbSNP
14g.28768156A>GCA389476053FOXG1c.877A>G (p.Thr293Ala)
gnomAD v4
14g.28768156A>TCA389476054FOXG1c.877A>T (p.Thr293Ser)
14g.28768157C>ACA389476055FOXG1c.878C>A (p.Thr293Asn)
14g.28768157C>GCA389476056FOXG1c.878C>G (p.Thr293Ser)
14g.28768157C>TCA389476057FOXG1c.878C>T (p.Thr293Ile)
14g.28768158C>ACA486098214FOXG1c.879C>A (p.Thr293=)
gnomAD v4
14g.28768158C=CA2126000304FOXG1c.879C= (p.Thr293=)
14g.28768158C>GCA486098215FOXG1c.879C>G (p.Thr293=)
dbSNP gnomAD v2 gnomAD v4
14g.28768158C>TCA486098216FOXG1c.879C>T (p.Thr293=)
gnomAD v4
14g.28768159T>ACA389476059FOXG1c.880T>A (p.Ser294Thr)
14g.28768159T>CCA314628FOXG1c.880T>C (p.Ser294Pro)
ClinVar dbSNP
14g.28768159T>GCA389476058FOXG1c.880T>G (p.Ser294Ala)
14g.28768159T=CA2126000305FOXG1c.880T= (p.Ser294=)
14g.28768160C>ACA389476060FOXG1c.881C>A (p.Ser294Tyr)
COSMIC
14g.28768160C>GCA389476061FOXG1c.881C>G (p.Ser294Cys)
14g.28768160C>TCA389476062FOXG1c.881C>T (p.Ser294Phe)
14g.28768161C>ACA486098221FOXG1c.882C>A (p.Ser294=)
14g.28768161C>GCA486098222FOXG1c.882C>G (p.Ser294=)
14g.28768161C>TCA486098223FOXG1c.882C>T (p.Ser294=)
gnomAD v4
14g.28768162A=CA2126000306FOXG1c.883A= (p.Thr295=)
14g.28768162A>CCA389476063FOXG1c.883A>C (p.Thr295Pro)
14g.28768162A>GCA389476064FOXG1c.883A>G (p.Thr295Ala)
14g.28768162A>TCA389476065FOXG1c.883A>T (p.Thr295Ser)
14g.28768163C>ACA389476066FOXG1c.884C>A (p.Thr295Asn)
14g.28768163C>GCA389476067FOXG1c.884C>G (p.Thr295Ser)
14g.28768163C>TCA389476068FOXG1c.884C>T (p.Thr295Ile)
14g.28768164dupCA16043741FOXG1c.885dup (p.Gly296ArgfsTer?)
ClinVar dbSNP
14g.28768164C>ACA486098226FOXG1c.885C>A (p.Thr295=)
dbSNP gnomAD v3 gnomAD v4
14g.28768164C=CA2126000307FOXG1c.885C= (p.Thr295=)
14g.28768164C>GCA486098225FOXG1c.885C>G (p.Thr295=)
gnomAD v4
14g.28768164C>TCA7140637FOXG1c.885C>T (p.Thr295=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.28768165G>ACA389476069FOXG1c.886G>A (p.Gly296Ser)
ClinVar gnomAD v4
14g.28768165G>CCA389476070FOXG1c.886G>C (p.Gly296Arg)
14g.28768165G>TCA389476071FOXG1c.886G>T (p.Gly296Cys)
14g.28768166delCA2840770144FOXG1c.887del (p.Gly296AlafsTer30)
14g.28768166G>ACA389476074FOXG1c.887G>A (p.Gly296Asp)
14g.28768166G>CCA389476073FOXG1c.887G>C (p.Gly296Ala)
14g.28768166G=CA2126000308FOXG1c.887G= (p.Gly296=)
14g.28768166G>TCA389476072FOXG1c.887G>T (p.Gly296Val)
ClinVar dbSNP
14g.28768167C>ACA486098231FOXG1c.888C>A (p.Gly296=)
14g.28768167C>GCA486098232FOXG1c.888C>G (p.Gly296=)
14g.28768167C>TCA486098233FOXG1c.888C>T (p.Gly296=)
14g.28768168C>ACA389476076FOXG1c.889C>A (p.Leu297Ile)
COSMIC
14g.28768168C>GCA389476075FOXG1c.889C>G (p.Leu297Val)
14g.28768168C>TCA389476077FOXG1c.889C>T (p.Leu297Phe)
gnomAD v4
14g.28768169T>ACA389476078FOXG1c.890T>A (p.Leu297His)
COSMIC
14g.28768169T>CCA389476079FOXG1c.890T>C (p.Leu297Pro)
14g.28768169T>GCA389476080FOXG1c.890T>G (p.Leu297Arg)
14g.28768170C>ACA486098236FOXG1c.891C>A (p.Leu297=)
14g.28768170C=CA2126000309FOXG1c.891C= (p.Leu297=)
14g.28768170C>GCA486098234FOXG1c.891C>G (p.Leu297=)
COSMIC
14g.28768170C>TCA486098238FOXG1c.891C>T (p.Leu297=)
dbSNP gnomAD v2 gnomAD v4
14g.28768171A>CCA389476081FOXG1c.892A>C (p.Thr298Pro)
14g.28768171A>GCA389476082FOXG1c.892A>G (p.Thr298Ala)
14g.28768171A>TCA389476083FOXG1c.892A>T (p.Thr298Ser)
14g.28768172C>ACA389476084FOXG1c.893C>A (p.Thr298Asn)
14g.28768172C>GCA389476085FOXG1c.893C>G (p.Thr298Ser)
ClinVar dbSNP
14g.28768172C>TCA389476086FOXG1c.893C>T (p.Thr298Ile)
14g.28768173C>ACA486098240FOXG1c.894C>A (p.Thr298=)
14g.28768173C=CA2126000310FOXG1c.894C= (p.Thr298=)
14g.28768173C>GCA486098241FOXG1c.894C>G (p.Thr298=)
dbSNP gnomAD v2 gnomAD v4
14g.28768173C>TCA486098242FOXG1c.894C>T (p.Thr298=)
gnomAD v4
14g.28768174T>ACA389476087FOXG1c.895T>A (p.Phe299Ile)
14g.28768174T>CCA389476088FOXG1c.895T>C (p.Phe299Leu)
14g.28768174T>GCA389476089FOXG1c.895T>G (p.Phe299Val)
14g.28768175T>ACA389476092FOXG1c.896T>A (p.Phe299Tyr)
14g.28768175T>CCA389476090FOXG1c.896T>C (p.Phe299Ser)
14g.28768175T>GCA389476091FOXG1c.896T>G (p.Phe299Cys)
14g.28768176C>ACA389476093FOXG1c.897C>A (p.Phe299Leu)
14g.28768176C=CA2126000311FOXG1c.897C= (p.Phe299=)
14g.28768176C>GCA389476094FOXG1c.897C>G (p.Phe299Leu)
14g.28768176C>TCA486098247FOXG1c.897C>T (p.Phe299=)
dbSNP gnomAD v2 COSMIC
14g.28768177A>CCA389476095FOXG1c.898A>C (p.Met300Leu)
14g.28768177A>GCA389476096FOXG1c.898A>G (p.Met300Val)
gnomAD v4
14g.28768177A>TCA389476097FOXG1c.898A>T (p.Met300Leu)
14g.28768178T>ACA389476098FOXG1c.899T>A (p.Met300Lys)
gnomAD v3 gnomAD v4
14g.28768178T>CCA389476099FOXG1c.899T>C (p.Met300Thr)
14g.28768178T>GCA389476100FOXG1c.899T>G (p.Met300Arg)

Number of alleles fetched