Chr Mutation (hg38) CAid Gene Transcript Linkouts
14g.28767909C>ACA389475519FOXG1c.630C>A (p.Phe210Leu)
14g.28767909C>GCA389475520FOXG1c.630C>G (p.Phe210Leu)
14g.28767909C>TCA486098501FOXG1c.630C>T (p.Phe210=)
gnomAD v4
14g.28767910A>CCA389475522FOXG1c.631A>C (p.Ile211Leu)
14g.28767910A>GCA389475523FOXG1c.631A>G (p.Ile211Val)
14g.28767910A>TCA389475521FOXG1c.631A>T (p.Ile211Phe)
gnomAD v3 gnomAD v4
14g.28767911T>ACA389475524FOXG1c.632T>A (p.Ile211Asn)
ClinVar dbSNP
14g.28767911T>CCA389475525FOXG1c.632T>C (p.Ile211Thr)
ClinVar dbSNP gnomAD v4 COSMIC
14g.28767911T>GCA389475526FOXG1c.632T>G (p.Ile211Ser)
14g.28767911T=CA2125999874FOXG1c.632T= (p.Ile211=)
14g.28767912C>ACA486098505FOXG1c.633C>A (p.Ile211=)
14g.28767912C>GCA389475527FOXG1c.633C>G (p.Ile211Met)
14g.28767912C>TCA486098507FOXG1c.633C>T (p.Ile211=)
gnomAD v4
14g.28767913delCA2573053896FOXG1c.634del (p.Met212Ter)
ClinVar dbSNP
14g.28767913A>CCA389475528FOXG1c.634A>C (p.Met212Leu)
14g.28767913A>GCA389475529FOXG1c.634A>G (p.Met212Val)
14g.28767913A>TCA389475530FOXG1c.634A>T (p.Met212Leu)
14g.28767914_28767919delCA2580088013FOXG1c.635_640del (p.Met212_Lys213del)
ClinVar
14g.28767914T>ACA389475531FOXG1c.635T>A (p.Met212Lys)
14g.28767914T>CCA389475532FOXG1c.635T>C (p.Met212Thr)
ClinVar dbSNP
14g.28767914T>GCA389475533FOXG1c.635T>G (p.Met212Arg)
14g.28767915G>ACA389475534FOXG1c.636G>A (p.Met212Ile)
14g.28767915G>CCA389475535FOXG1c.636G>C (p.Met212Ile)
14g.28767915G>TCA389475536FOXG1c.636G>T (p.Met212Ile)
14g.28767916A>CCA389475539FOXG1c.637A>C (p.Lys213Gln)
14g.28767916A>GCA389475538FOXG1c.637A>G (p.Lys213Glu)
14g.28767916A>TCA389475537FOXG1c.637A>T (p.Lys213Ter)
ClinVar
14g.28767917A>CCA389475540FOXG1c.638A>C (p.Lys213Thr)
14g.28767917A>GCA389475541FOXG1c.638A>G (p.Lys213Arg)
gnomAD v4
14g.28767917A>TCA389475542FOXG1c.638A>T (p.Lys213Met)
gnomAD v3 gnomAD v4
14g.28767918G>ACA486098517FOXG1c.639G>A (p.Lys213=)
ClinVar dbSNP COSMIC
14g.28767918G>CCA389475543FOXG1c.639G>C (p.Lys213Asn)
14g.28767918G=CA2125999880FOXG1c.639G= (p.Lys213=)
14g.28767918G>TCA389475544FOXG1c.639G>T (p.Lys213Asn)
14g.28767919A>CCA389475545FOXG1c.640A>C (p.Asn214His)
14g.28767919A>GCA389475546FOXG1c.640A>G (p.Asn214Asp)
14g.28767919A>TCA389475547FOXG1c.640A>T (p.Asn214Tyr)
14g.28767920A>CCA389475548FOXG1c.641A>C (p.Asn214Thr)
14g.28767920A>GCA389475549FOXG1c.641A>G (p.Asn214Ser)
14g.28767920A>TCA389475550FOXG1c.641A>T (p.Asn214Ile)
14g.28767921C>ACA389475551FOXG1c.642C>A (p.Asn214Lys)
14g.28767921C=CA2125999884FOXG1c.642C= (p.Asn214=)
14g.28767921C>GCA389475552FOXG1c.642C>G (p.Asn214Lys)
14g.28767921C>TCA486098521FOXG1c.642C>T (p.Asn214=)
ClinVar dbSNP
14g.28767922T>ACA389475554FOXG1c.643T>A (p.Phe215Ile)
ClinVar
14g.28767922T>CCA123554FOXG1c.643T>C (p.Phe215Leu)
ClinVar dbSNP
14g.28767922T>GCA389475553FOXG1c.643T>G (p.Phe215Val)
14g.28767922T=CA2125999890FOXG1c.643T= (p.Phe215=)
14g.28767923T>ACA389475555FOXG1c.644T>A (p.Phe215Tyr)
14g.28767923T>CCA389475556FOXG1c.644T>C (p.Phe215Ser)
14g.28767923T>GCA389475557FOXG1c.644T>G (p.Phe215Cys)
14g.28767923_28767924delinsCTCA207940FOXG1c.644_645delinsCT (p.Phe215Ser)
ClinVar dbSNP
14g.28767923_28767924delinsTCCA2125999895FOXG1c.644_645delinsTC (p.Phe215=)
14g.28767924C>ACA389475558FOXG1c.645C>A (p.Phe215Leu)
ClinVar dbSNP
14g.28767924C=CA2125999900FOXG1c.645C= (p.Phe215=)
14g.28767924C>GCA16042954FOXG1c.645C>G (p.Phe215Leu)
ClinVar dbSNP
14g.28767924C>TCA486098527FOXG1c.645C>T (p.Phe215=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
14g.28767926delCA2695219194FOXG1c.647del (p.Pro216LeufsTer25)
14g.28767924_28767932delinsCCCTTACTACA2125999899FOXG1c.645_653delinsCCCTTACTA (p.Phe215=)
14g.28767925C>ACA389475560FOXG1c.646C>A (p.Pro216Thr)
14g.28767925C=CA2125999907FOXG1c.646C= (p.Pro216=)
14g.28767925C>GCA389475559FOXG1c.646C>G (p.Pro216Ala)
14g.28767925C>TCA7140623FOXG1c.646C>T (p.Pro216Ser)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.28767927_28767934delCA234033FOXG1c.648_655del (p.Tyr217ArgfsTer?)
ClinVar dbSNP
14g.28767926C>ACA389475561FOXG1c.647C>A (p.Pro216His)
14g.28767926C>GCA389475562FOXG1c.647C>G (p.Pro216Arg)
14g.28767926C>TCA389475563FOXG1c.647C>T (p.Pro216Leu)
14g.28767927T>ACA486098538FOXG1c.648T>A (p.Pro216=)
ClinVar dbSNP gnomAD v4
14g.28767927T>CCA486098539FOXG1c.648T>C (p.Pro216=)
dbSNP
14g.28767927T>GCA486098543FOXG1c.648T>G (p.Pro216=)
14g.28767927_28767928insATCA2579988444FOXG1c.648_649insAT (p.Tyr217IlefsTer25)
14g.28767928T>ACA389475566FOXG1c.649T>A (p.Tyr217Asn)
14g.28767928T>CCA389475564FOXG1c.649T>C (p.Tyr217His)
14g.28767928T>GCA389475565FOXG1c.649T>G (p.Tyr217Asp)
14g.28767929A>CCA389475567FOXG1c.650A>C (p.Tyr217Ser)
14g.28767929A>GCA389475568FOXG1c.650A>G (p.Tyr217Cys)
14g.28767929A>TCA389475569FOXG1c.650A>T (p.Tyr217Phe)
14g.28767930C>ACA389475570FOXG1c.651C>A (p.Tyr217Ter)
14g.28767930C=CA2125999910FOXG1c.651C= (p.Tyr217=)
14g.28767930C>GCA314612FOXG1c.651C>G (p.Tyr217Ter)
ClinVar dbSNP
14g.28767930C>TCA486098546FOXG1c.651C>T (p.Tyr217=)
ClinVar dbSNP
14g.28767931T>ACA389475573FOXG1c.652T>A (p.Tyr218Asn)
14g.28767931T>CCA389475571FOXG1c.652T>C (p.Tyr218His)
14g.28767931T>GCA389475572FOXG1c.652T>G (p.Tyr218Asp)
14g.28767932A=CA2125999917FOXG1c.653A= (p.Tyr218=)
14g.28767932A>CCA389475574FOXG1c.653A>C (p.Tyr218Ser)
14g.28767932A>GCA389475575FOXG1c.653A>G (p.Tyr218Cys)
ClinVar dbSNP
14g.28767932A>TCA389475576FOXG1c.653A>T (p.Tyr218Phe)
14g.28767933C>ACA389475577FOXG1c.654C>A (p.Tyr218Ter)
ClinVar dbSNP
14g.28767933C>GCA389475578FOXG1c.654C>G (p.Tyr218Ter)
14g.28767933C>TCA486098559FOXG1c.654C>T (p.Tyr218=)
14g.28767934delCA2801003776FOXG1c.655del (p.Arg219AlafsTer22)
14g.28767934C>ACA389475579FOXG1c.655C>A (p.Arg219Ser)
14g.28767934C=CA2125999921FOXG1c.655C= (p.Arg219=)
14g.28767934C>GCA389475580FOXG1c.655C>G (p.Arg219Gly)
ClinVar dbSNP
14g.28767934C>TCA389475581FOXG1c.655C>T (p.Arg219Cys)
dbSNP gnomAD v4 COSMIC
14g.28767935G>ACA389475582FOXG1c.656G>A (p.Arg219His)
dbSNP
14g.28767935G>CCA389475583FOXG1c.656G>C (p.Arg219Pro)
dbSNP
14g.28767935G=CA2125999925FOXG1c.656G= (p.Arg219=)
14g.28767935G>TCA389475584FOXG1c.656G>T (p.Arg219Leu)
14g.28767936C>ACA486098567FOXG1c.657C>A (p.Arg219=)
14g.28767936C=CA2125999930FOXG1c.657C= (p.Arg219=)
14g.28767936C>GCA486098568FOXG1c.657C>G (p.Arg219=)
ClinVar dbSNP gnomAD v4
14g.28767936C>TCA7140624FOXG1c.657C>T (p.Arg219=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
14g.28767937G>ACA389475585FOXG1c.658G>A (p.Glu220Lys)
14g.28767937G>CCA389475587FOXG1c.658G>C (p.Glu220Gln)
14g.28767937G>TCA389475586FOXG1c.658G>T (p.Glu220Ter)
14g.28767938A>CCA389475588FOXG1c.659A>C (p.Glu220Ala)
14g.28767938A>GCA389475589FOXG1c.659A>G (p.Glu220Gly)
14g.28767938A>TCA389475590FOXG1c.659A>T (p.Glu220Val)
14g.28767939G>ACA486098575FOXG1c.660G>A (p.Glu220=)
ClinVar dbSNP
14g.28767939G>CCA389475591FOXG1c.660G>C (p.Glu220Asp)
14g.28767939G=CA2125999935FOXG1c.660G= (p.Glu220=)
14g.28767939G>TCA389475592FOXG1c.660G>T (p.Glu220Asp)
dbSNP
14g.28767940A>CCA389475593FOXG1c.661A>C (p.Asn221His)
14g.28767940A>GCA389475594FOXG1c.661A>G (p.Asn221Asp)
14g.28767940A>TCA389475595FOXG1c.661A>T (p.Asn221Tyr)
14g.28767941A>CCA389475596FOXG1c.662A>C (p.Asn221Thr)
14g.28767941A>GCA389475597FOXG1c.662A>G (p.Asn221Ser)
gnomAD v4
14g.28767941A>TCA389475598FOXG1c.662A>T (p.Asn221Ile)
14g.28767942C>ACA389475599FOXG1c.663C>A (p.Asn221Lys)
14g.28767942C>GCA389475600FOXG1c.663C>G (p.Asn221Lys)
14g.28767942C>TCA486098582FOXG1c.663C>T (p.Asn221=)
14g.28767943A>CCA389475601FOXG1c.664A>C (p.Lys222Gln)
14g.28767943A>GCA389475603FOXG1c.664A>G (p.Lys222Glu)
14g.28767943A>TCA389475602FOXG1c.664A>T (p.Lys222Ter)
14g.28767944A>CCA389475604FOXG1c.665A>C (p.Lys222Thr)
14g.28767944A>GCA389475605FOXG1c.665A>G (p.Lys222Arg)
14g.28767944A>TCA389475606FOXG1c.665A>T (p.Lys222Met)
14g.28767945G>ACA486098592FOXG1c.666G>A (p.Lys222=)
14g.28767945G>CCA389475607FOXG1c.666G>C (p.Lys222Asn)
14g.28767945G>TCA389475608FOXG1c.666G>T (p.Lys222Asn)
14g.28767946C>ACA389475609FOXG1c.667C>A (p.Gln223Lys)
14g.28767946C=CA2125999937FOXG1c.667C= (p.Gln223=)
14g.28767946C>GCA389475610FOXG1c.667C>G (p.Gln223Glu)
14g.28767946C>TCA314614FOXG1c.667C>T (p.Gln223Ter)
ClinVar dbSNP
14g.28767947A>CCA389475611FOXG1c.668A>C (p.Gln223Pro)
14g.28767947A>GCA389475612FOXG1c.668A>G (p.Gln223Arg)
14g.28767947A>TCA389475613FOXG1c.668A>T (p.Gln223Leu)
14g.28767948G>ACA486098601FOXG1c.669G>A (p.Gln223=)
COSMIC
14g.28767948G>CCA389475614FOXG1c.669G>C (p.Gln223His)
14g.28767948G>TCA389475615FOXG1c.669G>T (p.Gln223His)
14g.28767949G>ACA234034FOXG1c.670G>A (p.Gly224Ser)
ClinVar dbSNP
14g.28767949G>CCA389475617FOXG1c.670G>C (p.Gly224Arg)
14g.28767949G=CA2125999941FOXG1c.670G= (p.Gly224=)
14g.28767949G>TCA389475616FOXG1c.670G>T (p.Gly224Cys)
14g.28767950G>ACA314648FOXG1c.671G>A (p.Gly224Asp)
ClinVar dbSNP
14g.28767950G>CCA389475618FOXG1c.671G>C (p.Gly224Ala)
14g.28767950G=CA2125999945FOXG1c.671G= (p.Gly224=)
14g.28767950G>TCA389475619FOXG1c.671G>T (p.Gly224Val)
14g.28767951C>ACA486098613FOXG1c.672C>A (p.Gly224=)
14g.28767951C=CA2125999950FOXG1c.672C= (p.Gly224=)
14g.28767951C>GCA172189FOXG1c.672C>G (p.Gly224=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.28767951C>TCA486098617FOXG1c.672C>T (p.Gly224=)
dbSNP gnomAD v2 gnomAD v4
14g.28767952T>ACA389475620FOXG1c.673T>A (p.Trp225Arg)
14g.28767952T>CCA314650FOXG1c.673T>C (p.Trp225Arg)
dbSNP
14g.28767952T>GCA389475621FOXG1c.673T>G (p.Trp225Gly)
ClinVar
14g.28767952T=CA2125999952FOXG1c.673T= (p.Trp225=)
14g.28767953G>ACA389475622FOXG1c.674G>A (p.Trp225Ter)
14g.28767953G>CCA16621656FOXG1c.674G>C (p.Trp225Ser)
ClinVar dbSNP
14g.28767953G=CA2125999955FOXG1c.674G= (p.Trp225=)
14g.28767953G>TCA389475623FOXG1c.674G>T (p.Trp225Leu)
14g.28767954G>ACA314616FOXG1c.675G>A (p.Trp225Ter)
dbSNP
14g.28767954G>CCA389475625FOXG1c.675G>C (p.Trp225Cys)
14g.28767954G=CA2125999957FOXG1c.675G= (p.Trp225=)
14g.28767954G>TCA389475624FOXG1c.675G>T (p.Trp225Cys)
14g.28767955C>ACA389475626FOXG1c.676C>A (p.Gln226Lys)
14g.28767955C=CA2125999961FOXG1c.676C= (p.Gln226=)
14g.28767955C>GCA389475627FOXG1c.676C>G (p.Gln226Glu)
ClinVar
14g.28767955C>TCA389475628FOXG1c.676C>T (p.Gln226Ter)
ClinVar dbSNP
14g.28767956A>CCA389475629FOXG1c.677A>C (p.Gln226Pro)
ClinVar
14g.28767956A>GCA389475630FOXG1c.677A>G (p.Gln226Arg)
14g.28767956A>TCA389475631FOXG1c.677A>T (p.Gln226Leu)
14g.28767957G>ACA486098636FOXG1c.678G>A (p.Gln226=)
14g.28767957G>CCA389475632FOXG1c.678G>C (p.Gln226His)
14g.28767957G>TCA389475633FOXG1c.678G>T (p.Gln226His)
14g.28767958A=CA2125999967FOXG1c.679A= (p.Asn227=)
14g.28767958A>CCA389475634FOXG1c.679A>C (p.Asn227His)
14g.28767958A>GCA389475635FOXG1c.679A>G (p.Asn227Asp)
ClinVar dbSNP
14g.28767958A>TCA389475636FOXG1c.679A>T (p.Asn227Tyr)
14g.28767959A>CCA389475638FOXG1c.680A>C (p.Asn227Thr)
14g.28767959A>GCA389475639FOXG1c.680A>G (p.Asn227Ser)
ClinVar
14g.28767959A>TCA389475637FOXG1c.680A>T (p.Asn227Ile)
ClinVar
14g.28767960C>ACA389475640FOXG1c.681C>A (p.Asn227Lys)
14g.28767960C=CA2125999970FOXG1c.681C= (p.Asn227=)
14g.28767960C>GCA199447FOXG1c.681C>G (p.Asn227Lys)
ClinVar dbSNP
14g.28767960C>TCA486098659FOXG1c.681C>T (p.Asn227=)
ClinVar
14g.28767961T>ACA389475641FOXG1c.682T>A (p.Ser228Thr)
14g.28767961T>CCA389475642FOXG1c.682T>C (p.Ser228Pro)
dbSNP gnomAD v2 gnomAD v4
14g.28767961T>GCA389475643FOXG1c.682T>G (p.Ser228Ala)
14g.28767961T=CA2125999973FOXG1c.682T= (p.Ser228=)
14g.28767962C>ACA389475644FOXG1c.683C>A (p.Ser228Tyr)
14g.28767962C>GCA389475645FOXG1c.683C>G (p.Ser228Cys)
ClinVar
14g.28767962C>TCA389475646FOXG1c.683C>T (p.Ser228Phe)
14g.28767963C>ACA486098680FOXG1c.684C>A (p.Ser228=)
gnomAD v3 gnomAD v4
14g.28767963C=CA2125999976FOXG1c.684C= (p.Ser228=)
14g.28767963C>GCA486098704FOXG1c.684C>G (p.Ser228=)
14g.28767963C>TCA7140625FOXG1c.684C>T (p.Ser228=)
dbSNP ExAC gnomAD v2 gnomAD v4
14g.28767964A=CA2125999978FOXG1c.685A= (p.Ile229=)
14g.28767964A>CCA16621657FOXG1c.685A>C (p.Ile229Leu)
ClinVar dbSNP
14g.28767964A>GCA389475647FOXG1c.685A>G (p.Ile229Val)
14g.28767964A>TCA389475648FOXG1c.685A>T (p.Ile229Phe)
14g.28767964_28767965delCA645570773FOXG1c.685_686del (p.Ile229ProfsTer?)
COSMIC
14g.28767965T>ACA314618FOXG1c.686T>A (p.Ile229Asn)
dbSNP
14g.28767965T>CCA258396578FOXG1c.686T>C (p.Ile229Thr)
dbSNP gnomAD v2 gnomAD v4
14g.28767965T>GCA389475649FOXG1c.686T>G (p.Ile229Ser)
14g.28767965T=CA2125999981FOXG1c.686T= (p.Ile229=)
14g.28767965_28767966delinsAACA2499222615FOXG1c.686_687delinsAA (p.Ile229Lys)
ClinVar dbSNP
14g.28767966C>ACA486098718FOXG1c.687C>A (p.Ile229=)
14g.28767966C>GCA389475650FOXG1c.687C>G (p.Ile229Met)
14g.28767966C>TCA486098721FOXG1c.687C>T (p.Ile229=)
14g.28767967C>ACA389475651FOXG1c.688C>A (p.Arg230Ser)
gnomAD v3 gnomAD v4
14g.28767967C=CA2125999986FOXG1c.688C= (p.Arg230=)
14g.28767967C>GCA389475652FOXG1c.688C>G (p.Arg230Gly)
COSMIC
14g.28767967C>TCA389475653FOXG1c.688C>T (p.Arg230Cys)
ClinVar dbSNP
14g.28767968G>ACA199440FOXG1c.689G>A (p.Arg230His)
ClinVar dbSNP COSMIC
14g.28767968G>CCA389475654FOXG1c.689G>C (p.Arg230Pro)
14g.28767968G=CA2125999994FOXG1c.689G= (p.Arg230=)
14g.28767968G>TCA10606123FOXG1c.689G>T (p.Arg230Leu)
ClinVar dbSNP
14g.28767969C>ACA486098726FOXG1c.690C>A (p.Arg230=)
14g.28767969C=CA2126000003FOXG1c.690C= (p.Arg230=)
14g.28767969C>GCA486098729FOXG1c.690C>G (p.Arg230=)
gnomAD v3 gnomAD v4
14g.28767969C>TCA7140626FOXG1c.690C>T (p.Arg230=)
dbSNP ExAC gnomAD v2 gnomAD v4
14g.28767969_28767976dupCA2573149902FOXG1c.690_697dup (p.Leu233ProfsTer11)
ClinVar dbSNP
14g.28767970C>ACA389475655FOXG1c.691C>A (p.His231Asn)
14g.28767970C>GCA389475656FOXG1c.691C>G (p.His231Asp)
14g.28767970C>TCA389475657FOXG1c.691C>T (p.His231Tyr)
14g.28767971A>CCA389475658FOXG1c.692A>C (p.His231Pro)
14g.28767971A>GCA389475659FOXG1c.692A>G (p.His231Arg)
ClinVar dbSNP
14g.28767971A>TCA389475660FOXG1c.692A>T (p.His231Leu)
14g.28767972C>ACA389475661FOXG1c.693C>A (p.His231Gln)
14g.28767972C>GCA389475662FOXG1c.693C>G (p.His231Gln)
dbSNP
14g.28767972C>TCA486098734FOXG1c.693C>T (p.His231=)
14g.28767973A=CA2126000009FOXG1c.694A= (p.Asn232=)
14g.28767973A>CCA389475663FOXG1c.694A>C (p.Asn232His)
14g.28767973A>GCA389475664FOXG1c.694A>G (p.Asn232Asp)
ClinVar dbSNP
14g.28767973A>TCA235903FOXG1c.694A>T (p.Asn232Tyr)
ClinVar dbSNP
14g.28767974A>CCA389475665FOXG1c.695A>C (p.Asn232Thr)
ClinVar
14g.28767974A>GCA389475667FOXG1c.695A>G (p.Asn232Ser)
ClinVar dbSNP
14g.28767974A>TCA389475666FOXG1c.695A>T (p.Asn232Ile)
14g.28767975T>ACA389475668FOXG1c.696T>A (p.Asn232Lys)
14g.28767975T>CCA486098741FOXG1c.696T>C (p.Asn232=)
ClinVar dbSNP gnomAD v2 COSMIC
14g.28767975T>GCA389475669FOXG1c.696T>G (p.Asn232Lys)
14g.28767975T=CA2126000019FOXG1c.696T= (p.Asn232=)
14g.28767976C>ACA389475670FOXG1c.697C>A (p.Leu233Met)
14g.28767976C>GCA389475671FOXG1c.697C>G (p.Leu233Val)
14g.28767976C>TCA486098744FOXG1c.697C>T (p.Leu233=)
gnomAD v4
14g.28767977T>ACA389475672FOXG1c.698T>A (p.Leu233Gln)
14g.28767977T>CCA389475673FOXG1c.698T>C (p.Leu233Pro)
14g.28767977T>GCA389475674FOXG1c.698T>G (p.Leu233Arg)
14g.28767978G>ACA486098747FOXG1c.699G>A (p.Leu233=)
gnomAD v4
14g.28767978G>CCA486098752FOXG1c.699G>C (p.Leu233=)
ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC
14g.28767978G>TCA486098749FOXG1c.699G>T (p.Leu233=)
ClinVar dbSNP gnomAD v4
14g.28767979T>ACA389475675FOXG1c.700T>A (p.Ser234Thr)
14g.28767979T>CCA199442FOXG1c.700T>C (p.Ser234Pro)
ClinVar dbSNP COSMIC
14g.28767979T>GCA389475676FOXG1c.700T>G (p.Ser234Ala)
COSMIC
14g.28767979T=CA2126000025FOXG1c.700T= (p.Ser234=)
14g.28767979_28767980delinsTCCA2126000028FOXG1c.700_701delinsTC (p.Ser234=)
14g.28767980C>ACA389475678FOXG1c.701C>A (p.Ser234Tyr)
14g.28767980C=CA2126000043FOXG1c.701C= (p.Ser234=)
14g.28767980C>GCA389475677FOXG1c.701C>G (p.Ser234Cys)
14g.28767980C>TCA314620FOXG1c.701C>T (p.Ser234Phe)
ClinVar dbSNP
14g.28767982delCA16619862FOXG1c.703del (p.Leu235SerfsTer6)
ClinVar dbSNP
14g.28767981C>ACA486098761FOXG1c.702C>A (p.Ser234=)
14g.28767981C>GCA486098764FOXG1c.702C>G (p.Ser234=)
14g.28767981C>TCA486098766FOXG1c.702C>T (p.Ser234=)
ClinVar dbSNP gnomAD v3 gnomAD v4
14g.28767982C>ACA389475679FOXG1c.703C>A (p.Leu235Ile)
14g.28767982C=CA2126000051FOXG1c.703C= (p.Leu235=)
14g.28767982C>GCA389475680FOXG1c.703C>G (p.Leu235Val)
14g.28767982C>TCA389475681FOXG1c.703C>T (p.Leu235Phe)
ClinVar dbSNP COSMIC
14g.28767983T>ACA389475682FOXG1c.704T>A (p.Leu235His)
14g.28767983T>CCA389475683FOXG1c.704T>C (p.Leu235Pro)
14g.28767983T>GCA389475684FOXG1c.704T>G (p.Leu235Arg)
14g.28767984C>ACA486098770FOXG1c.705C>A (p.Leu235=)
gnomAD v3 gnomAD v4
14g.28767984C>GCA486098773FOXG1c.705C>G (p.Leu235=)
14g.28767984C>TCA486098772FOXG1c.705C>T (p.Leu235=)
14g.28767987_28767989delCA2582341746FOXG1c.708_710del (p.Asn236del)
ClinVar
14g.28767985A>CCA389475685FOXG1c.706A>C (p.Asn236His)
14g.28767985A>GCA389475686FOXG1c.706A>G (p.Asn236Asp)
ClinVar
14g.28767985A>TCA389475687FOXG1c.706A>T (p.Asn236Tyr)
14g.28767986A>CCA389475688FOXG1c.707A>C (p.Asn236Thr)
14g.28767986A>GCA389475689FOXG1c.707A>G (p.Asn236Ser)
gnomAD v4
14g.28767986A>TCA389475690FOXG1c.707A>T (p.Asn236Ile)
14g.28767987C>ACA314622FOXG1c.708C>A (p.Asn236Lys)
ClinVar dbSNP
14g.28767987C=CA2126000057FOXG1c.708C= (p.Asn236=)
14g.28767987C>GCA389475691FOXG1c.708C>G (p.Asn236Lys)
14g.28767987C>TCA486098779FOXG1c.708C>T (p.Asn236=)
ClinVar dbSNP gnomAD v4
14g.28767988A>CCA389475692FOXG1c.709A>C (p.Lys237Gln)
14g.28767988A>GCA389475693FOXG1c.709A>G (p.Lys237Glu)
14g.28767988A>TCA389475694FOXG1c.709A>T (p.Lys237Ter)
14g.28767989A>CCA389475695FOXG1c.710A>C (p.Lys237Thr)
14g.28767989A>GCA389475696FOXG1c.710A>G (p.Lys237Arg)
14g.28767989A>TCA389475697FOXG1c.710A>T (p.Lys237Met)
14g.28767989_28767990insCACCAAACACACCCAACACACA2801003336FOXG1c.710_711insCACCAAACACACCCAACACA (p.Lys237AsnfsTer11)
14g.28767990G>ACA486098785FOXG1c.711G>A (p.Lys237=)
14g.28767990G>CCA389475698FOXG1c.711G>C (p.Lys237Asn)
14g.28767990G>TCA389475699FOXG1c.711G>T (p.Lys237Asn)
14g.28767991T>ACA389475700FOXG1c.712T>A (p.Cys238Ser)
gnomAD v3 gnomAD v4 COSMIC
14g.28767991T>CCA389475701FOXG1c.712T>C (p.Cys238Arg)
14g.28767991T>GCA389475702FOXG1c.712T>G (p.Cys238Gly)
14g.28767992G>ACA389475703FOXG1c.713G>A (p.Cys238Tyr)
ClinVar dbSNP
14g.28767992G>CCA389475704FOXG1c.713G>C (p.Cys238Ser)
14g.28767992G=CA2126000061FOXG1c.713G= (p.Cys238=)
14g.28767992G>TCA389475705FOXG1c.713G>T (p.Cys238Phe)
gnomAD v3 gnomAD v4
14g.28767993C>ACA389475706FOXG1c.714C>A (p.Cys238Ter)
14g.28767993C>GCA389475707FOXG1c.714C>G (p.Cys238Trp)
14g.28767993C>TCA486098799FOXG1c.714C>T (p.Cys238=)
ClinVar
14g.28767994T>ACA389475708FOXG1c.715T>A (p.Phe239Ile)
14g.28767994T>CCA389475709FOXG1c.715T>C (p.Phe239Leu)
14g.28767994T>GCA389475710FOXG1c.715T>G (p.Phe239Val)
14g.28767995T>ACA389475711FOXG1c.716T>A (p.Phe239Tyr)
14g.28767995T>CCA389475712FOXG1c.716T>C (p.Phe239Ser)
14g.28767995T>GCA389475713FOXG1c.716T>G (p.Phe239Cys)
14g.28767996C>ACA389475714FOXG1c.717C>A (p.Phe239Leu)
14g.28767996C=CA2126000065FOXG1c.717C= (p.Phe239=)
14g.28767996C>GCA389475715FOXG1c.717C>G (p.Phe239Leu)
ClinVar dbSNP
14g.28767996C>TCA486098815FOXG1c.717C>T (p.Phe239=)
ClinVar COSMIC
14g.28767997G>ACA389475716FOXG1c.718G>A (p.Val240Met)
14g.28767997G>CCA389475717FOXG1c.718G>C (p.Val240Leu)
14g.28767997G>TCA389475718FOXG1c.718G>T (p.Val240Leu)
14g.28767998T>ACA389475720FOXG1c.719T>A (p.Val240Glu)
14g.28767998T>CCA389475719FOXG1c.719T>C (p.Val240Ala)
14g.28767998T>GCA16619863FOXG1c.719T>G (p.Val240Gly)
ClinVar dbSNP
14g.28767998T=CA2126000070FOXG1c.719T= (p.Val240=)
14g.28767999G>ACA486098828FOXG1c.720G>A (p.Val240=)
ClinVar dbSNP gnomAD v2 gnomAD v4
14g.28767999G>CCA486098831FOXG1c.720G>C (p.Val240=)
ClinVar dbSNP gnomAD v3 gnomAD v4
14g.28767999G=CA2126000073FOXG1c.720G= (p.Val240=)
14g.28767999G>TCA486098829FOXG1c.720G>T (p.Val240=)
14g.28768000A=CA2126000076FOXG1c.721A= (p.Lys241=)
14g.28768000A>CCA389475721FOXG1c.721A>C (p.Lys241Gln)
14g.28768000A>GCA314652FOXG1c.721A>G (p.Lys241Glu)
dbSNP
14g.28768000A>TCA389475722FOXG1c.721A>T (p.Lys241Ter)
14g.28768001A>CCA389475723FOXG1c.722A>C (p.Lys241Thr)
14g.28768001A>GCA389475724FOXG1c.722A>G (p.Lys241Arg)
14g.28768001A>TCA389475725FOXG1c.722A>T (p.Lys241Met)
14g.28768002G>ACA486098835FOXG1c.723G>A (p.Lys241=)
14g.28768002G>CCA389475726FOXG1c.723G>C (p.Lys241Asn)
14g.28768002G>TCA389475727FOXG1c.723G>T (p.Lys241Asn)
14g.28768003G>ACA389475728FOXG1c.724G>A (p.Val242Met)
COSMIC
14g.28768003G>CCA389475729FOXG1c.724G>C (p.Val242Leu)
14g.28768003G>TCA389475730FOXG1c.724G>T (p.Val242Leu)
14g.28768004_28768010dupCA2580088018FOXG1c.725_731dup (p.His245AlafsTer?)
ClinVar
14g.28768004T>ACA389475731FOXG1c.725T>A (p.Val242Glu)
14g.28768004T>CCA389475732FOXG1c.725T>C (p.Val242Ala)
14g.28768004T>GCA389475733FOXG1c.725T>G (p.Val242Gly)
14g.28768005G>ACA486098844FOXG1c.726G>A (p.Val242=)
gnomAD v4 COSMIC
14g.28768005G>CCA486098848FOXG1c.726G>C (p.Val242=)
14g.28768005G>TCA486098845FOXG1c.726G>T (p.Val242=)
14g.28768006C>ACA389475736FOXG1c.727C>A (p.Pro243Thr)
14g.28768006C>GCA389475734FOXG1c.727C>G (p.Pro243Ala)
14g.28768006C>TCA389475735FOXG1c.727C>T (p.Pro243Ser)
gnomAD v4 COSMIC
14g.28768007C>ACA389475737FOXG1c.728C>A (p.Pro243Gln)
14g.28768007C=CA2126000078FOXG1c.728C= (p.Pro243=)
14g.28768007C>GCA389475738FOXG1c.728C>G (p.Pro243Arg)
dbSNP gnomAD v2 gnomAD v4
14g.28768007C>TCA389475740FOXG1c.728C>T (p.Pro243Leu)
COSMIC
14g.28768008G>ACA486098849FOXG1c.729G>A (p.Pro243=)
ClinVar dbSNP COSMIC
14g.28768008G>CCA7140627FOXG1c.729G>C (p.Pro243=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
14g.28768008G=CA2126000084FOXG1c.729G= (p.Pro243=)
14g.28768008G>TCA486098850FOXG1c.729G>T (p.Pro243=)
14g.28768009C>ACA389475741FOXG1c.730C>A (p.Arg244Ser)
gnomAD v3 gnomAD v4
14g.28768009C=CA2126000087FOXG1c.730C= (p.Arg244=)
14g.28768009C>GCA389475742FOXG1c.730C>G (p.Arg244Gly)
14g.28768009C>TCA199444FOXG1c.730C>T (p.Arg244Cys)
ClinVar dbSNP COSMIC

Number of alleles fetched