14 | g.28768072_28768087del | CA2573149903 | FOXG1 | c.793_808del (p.Phe265ArgfsTer?)
| ClinVar dbSNP |
14 | g.28768081_28768083del | CA2739277845 | FOXG1 | c.802_804del (p.Gly268del)
| ClinVar |
14 | g.28768078G>A | CA172199 | FOXG1 | c.799G>A (p.Gly267Ser)
| ClinVar dbSNP |
14 | g.28768078G>C | CA389475899 | FOXG1 | c.799G>C (p.Gly267Arg)
| |
14 | g.28768078G= | CA2126000267 | FOXG1 | c.799G= (p.Gly267=)
| |
14 | g.28768078G>T | CA389475900 | FOXG1 | c.799G>T (p.Gly267Cys)
| |
14 | g.28768079G>A | CA389475901 | FOXG1 | c.800G>A (p.Gly267Asp)
| ClinVar |
14 | g.28768079G>C | CA389475902 | FOXG1 | c.800G>C (p.Gly267Ala)
| |
14 | g.28768079G>T | CA389475903 | FOXG1 | c.800G>T (p.Gly267Val)
| |
14 | g.28768080C>A | CA486098949 | FOXG1 | c.801C>A (p.Gly267=)
| ClinVar dbSNP gnomAD v2 gnomAD v4 |
14 | g.28768080C= | CA2126000272 | FOXG1 | c.801C= (p.Gly267=)
| |
14 | g.28768080C>G | CA486098950 | FOXG1 | c.801C>G (p.Gly267=)
| |
14 | g.28768080C>T | CA486098951 | FOXG1 | c.801C>T (p.Gly267=)
| |
14 | g.28768081G>A | CA389475904 | FOXG1 | c.802G>A (p.Gly268Ser)
| COSMIC |
14 | g.28768081G>C | CA389475905 | FOXG1 | c.802G>C (p.Gly268Arg)
| COSMIC |
14 | g.28768081G>T | CA389475906 | FOXG1 | c.802G>T (p.Gly268Cys)
| |
14 | g.28768082del | CA2586963983 | FOXG1 | c.803del (p.Gly268AlafsTer?)
| ClinVar |
14 | g.28768082G>A | CA389475907 | FOXG1 | c.803G>A (p.Gly268Asp)
| |
14 | g.28768082G>C | CA389475908 | FOXG1 | c.803G>C (p.Gly268Ala)
| |
14 | g.28768082G>T | CA389475909 | FOXG1 | c.803G>T (p.Gly268Val)
| ClinVar dbSNP gnomAD v4 |
14 | g.28768083C>A | CA486098955 | FOXG1 | c.804C>A (p.Gly268=)
| gnomAD v4 |
14 | g.28768083C>G | CA486098957 | FOXG1 | c.804C>G (p.Gly268=)
| |
14 | g.28768083C>T | CA486098956 | FOXG1 | c.804C>T (p.Gly268=)
| ClinVar |
14 | g.28768084A>C | CA389475912 | FOXG1 | c.805A>C (p.Thr269Pro)
| gnomAD v4 |
14 | g.28768084A>G | CA389475910 | FOXG1 | c.805A>G (p.Thr269Ala)
| |
14 | g.28768084A>T | CA389475911 | FOXG1 | c.805A>T (p.Thr269Ser)
| |
14 | g.28768085C>A | CA389475913 | FOXG1 | c.806C>A (p.Thr269Asn)
| |
14 | g.28768085C>G | CA389475914 | FOXG1 | c.806C>G (p.Thr269Ser)
| |
14 | g.28768085C>T | CA389475915 | FOXG1 | c.806C>T (p.Thr269Ile)
| |
14 | g.28768086C>A | CA486098967 | FOXG1 | c.807C>A (p.Thr269=)
| |
14 | g.28768086C>G | CA486098968 | FOXG1 | c.807C>G (p.Thr269=)
| |
14 | g.28768086C>T | CA486098969 | FOXG1 | c.807C>T (p.Thr269=)
| gnomAD v4 |
14 | g.28768087A= | CA2126000273 | FOXG1 | c.808A= (p.Thr270=)
| |
14 | g.28768087A>C | CA389475916 | FOXG1 | c.808A>C (p.Thr270Pro)
| |
14 | g.28768087A>G | CA389475917 | FOXG1 | c.808A>G (p.Thr270Ala)
| dbSNP gnomAD v2 gnomAD v4 |
14 | g.28768087A>T | CA389475918 | FOXG1 | c.808A>T (p.Thr270Ser)
| |
14 | g.28768088C>A | CA389475919 | FOXG1 | c.809C>A (p.Thr270Lys)
| COSMIC |
14 | g.28768088C>G | CA389475920 | FOXG1 | c.809C>G (p.Thr270Arg)
| |
14 | g.28768088C>T | CA389475921 | FOXG1 | c.809C>T (p.Thr270Met)
| gnomAD v4 COSMIC |
14 | g.28768089G>A | CA7140631 | FOXG1 | c.810G>A (p.Thr270=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
14 | g.28768089G>C | CA486098973 | FOXG1 | c.810G>C (p.Thr270=)
| ClinVar gnomAD v4 |
14 | g.28768089G= | CA2126000274 | FOXG1 | c.810G= (p.Thr270=)
| |
14 | g.28768089G>T | CA486098975 | FOXG1 | c.810G>T (p.Thr270=)
| gnomAD v4 |
14 | g.28768090G>A | CA389475924 | FOXG1 | c.811G>A (p.Gly271Ser)
| ClinVar dbSNP |
14 | g.28768090G>C | CA389475923 | FOXG1 | c.811G>C (p.Gly271Arg)
| |
14 | g.28768090G= | CA2126000275 | FOXG1 | c.811G= (p.Gly271=)
| |
14 | g.28768090G>T | CA389475922 | FOXG1 | c.811G>T (p.Gly271Cys)
| ClinVar |
14 | g.28768091G>A | CA314624 | FOXG1 | c.812G>A (p.Gly271Asp)
| ClinVar dbSNP COSMIC |
14 | g.28768091G>C | CA389475925 | FOXG1 | c.812G>C (p.Gly271Ala)
| |
14 | g.28768091G= | CA2126000276 | FOXG1 | c.812G= (p.Gly271=)
| |
14 | g.28768091G>T | CA389475926 | FOXG1 | c.812G>T (p.Gly271Val)
| |
14 | g.28768092C>A | CA486098981 | FOXG1 | c.813C>A (p.Gly271=)
| |
14 | g.28768092C= | CA2126000277 | FOXG1 | c.813C= (p.Gly271=)
| |
14 | g.28768092C>G | CA486098982 | FOXG1 | c.813C>G (p.Gly271=)
| |
14 | g.28768092C>T | CA486098983 | FOXG1 | c.813C>T (p.Gly271=)
| dbSNP gnomAD v4 |
14 | g.28768093A>C | CA389475927 | FOXG1 | c.814A>C (p.Lys272Gln)
| |
14 | g.28768093A>G | CA389475928 | FOXG1 | c.814A>G (p.Lys272Glu)
| |
14 | g.28768093A>T | CA389475929 | FOXG1 | c.814A>T (p.Lys272Ter)
| |
14 | g.28768093_28768100del | CA2573332464 | FOXG1 | c.814_821del (p.Lys272AlafsTer?)
| ClinVar |
14 | g.28768094A>C | CA389475930 | FOXG1 | c.815A>C (p.Lys272Thr)
| |
14 | g.28768094A>G | CA389475931 | FOXG1 | c.815A>G (p.Lys272Arg)
| |
14 | g.28768094A>T | CA389475932 | FOXG1 | c.815A>T (p.Lys272Met)
| |
14 | g.28768095G>A | CA486098988 | FOXG1 | c.816G>A (p.Lys272=)
| |
14 | g.28768095G>C | CA389475933 | FOXG1 | c.816G>C (p.Lys272Asn)
| |
14 | g.28768095G>T | CA389475934 | FOXG1 | c.816G>T (p.Lys272Asn)
| gnomAD v4 |
14 | g.28768096C>A | CA389475935 | FOXG1 | c.817C>A (p.Leu273Met)
| gnomAD v4 |
14 | g.28768096C>G | CA389475936 | FOXG1 | c.817C>G (p.Leu273Val)
| |
14 | g.28768096C>T | CA486098991 | FOXG1 | c.817C>T (p.Leu273=)
| ClinVar |
14 | g.28768097T>A | CA389475937 | FOXG1 | c.818T>A (p.Leu273Gln)
| |
14 | g.28768097T>C | CA389475939 | FOXG1 | c.818T>C (p.Leu273Pro)
| |
14 | g.28768097T>G | CA389475938 | FOXG1 | c.818T>G (p.Leu273Arg)
| |
14 | g.28768098G>A | CA486098997 | FOXG1 | c.819G>A (p.Leu273=)
| ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.28768098G>C | CA486098998 | FOXG1 | c.819G>C (p.Leu273=)
| |
14 | g.28768098G= | CA2126000278 | FOXG1 | c.819G= (p.Leu273=)
| |
14 | g.28768098G>T | CA486099001 | FOXG1 | c.819G>T (p.Leu273=)
| gnomAD v4 |
14 | g.28768099C>A | CA486099003 | FOXG1 | c.820C>A (p.Arg274=)
| dbSNP gnomAD v2 gnomAD v4 |
14 | g.28768099C= | CA2126000279 | FOXG1 | c.820C= (p.Arg274=)
| |
14 | g.28768099C>G | CA389475940 | FOXG1 | c.820C>G (p.Arg274Gly)
| |
14 | g.28768099C>T | CA389475941 | FOXG1 | c.820C>T (p.Arg274Trp)
| gnomAD v4 COSMIC |
14 | g.28768100G>A | CA357167 | FOXG1 | c.821G>A (p.Arg274Gln)
| ClinVar dbSNP |
14 | g.28768100G>C | CA389475942 | FOXG1 | c.821G>C (p.Arg274Pro)
| ClinVar dbSNP |
14 | g.28768100G= | CA2126000280 | FOXG1 | c.821G= (p.Arg274=)
| |
14 | g.28768100G>T | CA389475943 | FOXG1 | c.821G>T (p.Arg274Leu)
| |
14 | g.28768101G>A | CA486099007 | FOXG1 | c.822G>A (p.Arg274=)
| dbSNP gnomAD v3 gnomAD v4 |
14 | g.28768101G>C | CA486099008 | FOXG1 | c.822G>C (p.Arg274=)
| |
14 | g.28768101G= | CA2126000281 | FOXG1 | c.822G= (p.Arg274=)
| |
14 | g.28768101G>T | CA486099009 | FOXG1 | c.822G>T (p.Arg274=)
| COSMIC |
14 | g.28768102C>A | CA389475944 | FOXG1 | c.823C>A (p.Arg275Ser)
| |
14 | g.28768102C>G | CA389475945 | FOXG1 | c.823C>G (p.Arg275Gly)
| |
14 | g.28768102C>T | CA389475946 | FOXG1 | c.823C>T (p.Arg275Cys)
| COSMIC |
14 | g.28768103G>A | CA389475947 | FOXG1 | c.824G>A (p.Arg275His)
| dbSNP |
14 | g.28768103G>C | CA389475948 | FOXG1 | c.824G>C (p.Arg275Pro)
| ClinVar dbSNP |
14 | g.28768103G= | CA2126000282 | FOXG1 | c.824G= (p.Arg275=)
| |
14 | g.28768103G>T | CA389475949 | FOXG1 | c.824G>T (p.Arg275Leu)
| |
14 | g.28768104C>A | CA486099016 | FOXG1 | c.825C>A (p.Arg275=)
| |
14 | g.28768104C>G | CA486099015 | FOXG1 | c.825C>G (p.Arg275=)
| |
14 | g.28768104C>T | CA486099014 | FOXG1 | c.825C>T (p.Arg275=)
| gnomAD v4 COSMIC |
14 | g.28768105C>A | CA389475951 | FOXG1 | c.826C>A (p.Arg276Ser)
| |
14 | g.28768105C>G | CA389475952 | FOXG1 | c.826C>G (p.Arg276Gly)
| |
14 | g.28768105C>T | CA389475950 | FOXG1 | c.826C>T (p.Arg276Cys)
| ClinVar dbSNP |
14 | g.28768106G>A | CA389475955 | FOXG1 | c.827G>A (p.Arg276His)
| dbSNP gnomAD v2 gnomAD v4 |
14 | g.28768106G>C | CA389475953 | FOXG1 | c.827G>C (p.Arg276Pro)
| |
14 | g.28768106G= | CA2126000283 | FOXG1 | c.827G= (p.Arg276=)
| |
14 | g.28768106G>T | CA389475954 | FOXG1 | c.827G>T (p.Arg276Leu)
| gnomAD v4 |
14 | g.28768107C>A | CA486099025 | FOXG1 | c.828C>A (p.Arg276=)
| |
14 | g.28768107C= | CA2126000284 | FOXG1 | c.828C= (p.Arg276=)
| |
14 | g.28768107C>G | CA486099024 | FOXG1 | c.828C>G (p.Arg276=)
| |
14 | g.28768107C>T | CA486099022 | FOXG1 | c.828C>T (p.Arg276=)
| dbSNP gnomAD v2 gnomAD v4 |
14 | g.28768108T>A | CA389475956 | FOXG1 | c.829T>A (p.Ser277Thr)
| |
14 | g.28768108T>C | CA389475957 | FOXG1 | c.829T>C (p.Ser277Pro)
| |
14 | g.28768108T>G | CA389475958 | FOXG1 | c.829T>G (p.Ser277Ala)
| |
14 | g.28768109C>A | CA389475959 | FOXG1 | c.830C>A (p.Ser277Tyr)
| |
14 | g.28768109C>G | CA389475960 | FOXG1 | c.830C>G (p.Ser277Cys)
| |
14 | g.28768109C>T | CA389475961 | FOXG1 | c.830C>T (p.Ser277Phe)
| |
14 | g.28768110C>A | CA486099033 | FOXG1 | c.831C>A (p.Ser277=)
| |
14 | g.28768110C>G | CA486099035 | FOXG1 | c.831C>G (p.Ser277=)
| |
14 | g.28768110C>T | CA486099034 | FOXG1 | c.831C>T (p.Ser277=)
| |
14 | g.28768111A>C | CA389475962 | FOXG1 | c.832A>C (p.Thr278Pro)
| |
14 | g.28768111A>G | CA389475963 | FOXG1 | c.832A>G (p.Thr278Ala)
| COSMIC |
14 | g.28768111A>T | CA389475964 | FOXG1 | c.832A>T (p.Thr278Ser)
| |
14 | g.28768112C>A | CA389475965 | FOXG1 | c.833C>A (p.Thr278Asn)
| |
14 | g.28768112C>G | CA389475966 | FOXG1 | c.833C>G (p.Thr278Ser)
| |
14 | g.28768112C>T | CA389475967 | FOXG1 | c.833C>T (p.Thr278Ile)
| gnomAD v4 |
14 | g.28768113C>A | CA486099042 | FOXG1 | c.834C>A (p.Thr278=)
| |
14 | g.28768113C= | CA2126000285 | FOXG1 | c.834C= (p.Thr278=)
| |
14 | g.28768113C>G | CA486099043 | FOXG1 | c.834C>G (p.Thr278=)
| |
14 | g.28768113C>T | CA7140632 | FOXG1 | c.834C>T (p.Thr278=)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
14 | g.28768114A>C | CA389475968 | FOXG1 | c.835A>C (p.Thr279Pro)
| |
14 | g.28768114A>G | CA389475969 | FOXG1 | c.835A>G (p.Thr279Ala)
| |
14 | g.28768114A>T | CA389475970 | FOXG1 | c.835A>T (p.Thr279Ser)
| |
14 | g.28768115C>A | CA389475971 | FOXG1 | c.836C>A (p.Thr279Asn)
| ClinVar gnomAD v4 COSMIC |
14 | g.28768115C>G | CA389475972 | FOXG1 | c.836C>G (p.Thr279Ser)
| |
14 | g.28768115C>T | CA389475973 | FOXG1 | c.836C>T (p.Thr279Ile)
| |
14 | g.28768116C>A | CA486099049 | FOXG1 | c.837C>A (p.Thr279=)
| |
14 | g.28768116C= | CA2126000286 | FOXG1 | c.837C= (p.Thr279=)
| |
14 | g.28768116C>G | CA486099051 | FOXG1 | c.837C>G (p.Thr279=)
| ClinVar dbSNP gnomAD v2 gnomAD v4 |
14 | g.28768116C>T | CA7140633 | FOXG1 | c.837C>T (p.Thr279=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
14 | g.28768117T>A | CA389475974 | FOXG1 | c.838T>A (p.Ser280Thr)
| |
14 | g.28768117T>C | CA389475975 | FOXG1 | c.838T>C (p.Ser280Pro)
| |
14 | g.28768117T>G | CA389475976 | FOXG1 | c.838T>G (p.Ser280Ala)
| |
14 | g.28768118C>A | CA389475977 | FOXG1 | c.839C>A (p.Ser280Ter)
| COSMIC |
14 | g.28768118C= | CA2126000287 | FOXG1 | c.839C= (p.Ser280=)
| |
14 | g.28768118C>G | CA389475978 | FOXG1 | c.839C>G (p.Ser280Trp)
| gnomAD v4 |
14 | g.28768118C>T | CA258396581 | FOXG1 | c.839C>T (p.Ser280Leu)
| dbSNP |
14 | g.28768119G>A | CA486099056 | FOXG1 | c.840G>A (p.Ser280=)
| gnomAD v4 |
14 | g.28768119G>C | CA486099057 | FOXG1 | c.840G>C (p.Ser280=)
| |
14 | g.28768119G= | CA2126000288 | FOXG1 | c.840G= (p.Ser280=)
| |
14 | g.28768119G>T | CA486099058 | FOXG1 | c.840G>T (p.Ser280=)
| dbSNP gnomAD v2 gnomAD v4 |
14 | g.28768120del | CA2580088020 | FOXG1 | c.841del (p.Arg281GlyfsTer?)
| ClinVar |
14 | g.28768120C>A | CA486099062 | FOXG1 | c.841C>A (p.Arg281=)
| |
14 | g.28768120C>G | CA389475980 | FOXG1 | c.841C>G (p.Arg281Gly)
| |
14 | g.28768120C>T | CA389475979 | FOXG1 | c.841C>T (p.Arg281Trp)
| COSMIC |
14 | g.28768121G>A | CA389475981 | FOXG1 | c.842G>A (p.Arg281Gln)
| |
14 | g.28768121G>C | CA389475982 | FOXG1 | c.842G>C (p.Arg281Pro)
| dbSNP COSMIC |
14 | g.28768121G= | CA2126000289 | FOXG1 | c.842G= (p.Arg281=)
| |
14 | g.28768121G>T | CA389475983 | FOXG1 | c.842G>T (p.Arg281Leu)
| |
14 | g.28768123dup | CA2573053898 | FOXG1 | c.844dup (p.Ala282GlyfsTer?)
| ClinVar dbSNP |
14 | g.28768122G>A | CA7140634 | FOXG1 | c.843G>A (p.Arg281=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.28768122G>C | CA486099066 | FOXG1 | c.843G>C (p.Arg281=)
| |
14 | g.28768122G= | CA2126000290 | FOXG1 | c.843G= (p.Arg281=)
| |
14 | g.28768122G>T | CA486099067 | FOXG1 | c.843G>T (p.Arg281=)
| COSMIC |
14 | g.28768123G>A | CA314626 | FOXG1 | c.844G>A (p.Ala282Thr)
| ClinVar dbSNP gnomAD v4 |
14 | g.28768123G>C | CA389475984 | FOXG1 | c.844G>C (p.Ala282Pro)
| |
14 | g.28768123G= | CA2126000291 | FOXG1 | c.844G= (p.Ala282=)
| |
14 | g.28768123G>T | CA389475985 | FOXG1 | c.844G>T (p.Ala282Ser)
| dbSNP gnomAD v2 gnomAD v4 |
14 | g.28768124C>A | CA389475986 | FOXG1 | c.845C>A (p.Ala282Asp)
| |
14 | g.28768124C>G | CA389475987 | FOXG1 | c.845C>G (p.Ala282Gly)
| |
14 | g.28768124C>T | CA389475988 | FOXG1 | c.845C>T (p.Ala282Val)
| COSMIC |
14 | g.28768125C>A | CA486099070 | FOXG1 | c.846C>A (p.Ala282=)
| gnomAD v4 |
14 | g.28768125C>G | CA486099071 | FOXG1 | c.846C>G (p.Ala282=)
| |
14 | g.28768125C>T | CA486099069 | FOXG1 | c.846C>T (p.Ala282=)
| |
14 | g.28768126A>C | CA389475989 | FOXG1 | c.847A>C (p.Lys283Gln)
| |
14 | g.28768126A>G | CA389475990 | FOXG1 | c.847A>G (p.Lys283Glu)
| |
14 | g.28768126A>T | CA389475991 | FOXG1 | c.847A>T (p.Lys283Ter)
| ClinVar |
14 | g.28768126_28768127insGACC | CA961450741 | FOXG1 | c.847_848insGACC (p.Lys283ArgfsTer?)
| gnomAD v3 gnomAD v4 |
14 | g.28768127A>C | CA389475993 | FOXG1 | c.848A>C (p.Lys283Thr)
| |
14 | g.28768127A>G | CA389475994 | FOXG1 | c.848A>G (p.Lys283Arg)
| COSMIC |
14 | g.28768127A>T | CA389475992 | FOXG1 | c.848A>T (p.Lys283Met)
| |
14 | g.28768128G>A | CA486099072 | FOXG1 | c.849G>A (p.Lys283=)
| ClinVar dbSNP gnomAD v3 gnomAD v4 |
14 | g.28768128G>C | CA389475995 | FOXG1 | c.849G>C (p.Lys283Asn)
| |
14 | g.28768128G= | CA2126000292 | FOXG1 | c.849G= (p.Lys283=)
| |
14 | g.28768128G>T | CA389475996 | FOXG1 | c.849G>T (p.Lys283Asn)
| |
14 | g.28768129C>A | CA389475997 | FOXG1 | c.850C>A (p.Leu284Met)
| |
14 | g.28768129C= | CA2126000293 | FOXG1 | c.850C= (p.Leu284=)
| |
14 | g.28768129C>G | CA389475998 | FOXG1 | c.850C>G (p.Leu284Val)
| |
14 | g.28768129C>T | CA258396582 | FOXG1 | c.850C>T (p.Leu284=)
| dbSNP gnomAD v4 |
14 | g.28768130T>A | CA389475999 | FOXG1 | c.851T>A (p.Leu284Gln)
| |
14 | g.28768130T>C | CA389476000 | FOXG1 | c.851T>C (p.Leu284Pro)
| |
14 | g.28768130T>G | CA389476001 | FOXG1 | c.851T>G (p.Leu284Arg)
| |
14 | g.28768131G>A | CA7140635 | FOXG1 | c.852G>A (p.Leu284=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.28768131G>C | CA486099074 | FOXG1 | c.852G>C (p.Leu284=)
| |
14 | g.28768131G= | CA2126000294 | FOXG1 | c.852G= (p.Leu284=)
| |
14 | g.28768131G>T | CA486099073 | FOXG1 | c.852G>T (p.Leu284=)
| gnomAD v4 |
14 | g.28768132G>A | CA389476002 | FOXG1 | c.853G>A (p.Ala285Thr)
| dbSNP |
14 | g.28768132G>C | CA389476003 | FOXG1 | c.853G>C (p.Ala285Pro)
| |
14 | g.28768132G= | CA2126000296 | FOXG1 | c.853G= (p.Ala285=)
| |
14 | g.28768132G>T | CA389476004 | FOXG1 | c.853G>T (p.Ala285Ser)
| |
14 | g.28768132_28768133delinsGC | CA2126000295 | FOXG1 | c.853_854delinsGC (p.Ala285=)
| |
14 | g.28768133C>A | CA389476005 | FOXG1 | c.854C>A (p.Ala285Asp)
| |
14 | g.28768133C>G | CA389476006 | FOXG1 | c.854C>G (p.Ala285Gly)
| |
14 | g.28768133C>T | CA389476007 | FOXG1 | c.854C>T (p.Ala285Val)
| |
14 | g.28768134del | CA658798197 | FOXG1 | c.855del (p.Phe286SerfsTer?)
| ClinVar dbSNP |
14 | g.28768134C>A | CA486099075 | FOXG1 | c.855C>A (p.Ala285=)
| gnomAD v4 |
14 | g.28768134C= | CA2126000297 | FOXG1 | c.855C= (p.Ala285=)
| |
14 | g.28768134C>G | CA486099077 | FOXG1 | c.855C>G (p.Ala285=)
| |
14 | g.28768134C>T | CA486099076 | FOXG1 | c.855C>T (p.Ala285=)
| dbSNP gnomAD v3 gnomAD v4 |
14 | g.28768135T>A | CA389476010 | FOXG1 | c.856T>A (p.Phe286Ile)
| |
14 | g.28768135T>C | CA389476009 | FOXG1 | c.856T>C (p.Phe286Leu)
| |
14 | g.28768135T>G | CA389476008 | FOXG1 | c.856T>G (p.Phe286Val)
| |
14 | g.28768136del | CA2695219196 | FOXG1 | c.857del (p.Phe286SerfsTer?)
| |
14 | g.28768136T>A | CA389476011 | FOXG1 | c.857T>A (p.Phe286Tyr)
| gnomAD v4 |
14 | g.28768136T>C | CA389476013 | FOXG1 | c.857T>C (p.Phe286Ser)
| |
14 | g.28768136T>G | CA389476012 | FOXG1 | c.857T>G (p.Phe286Cys)
| |
14 | g.28768137C>A | CA7140636 | FOXG1 | c.858C>A (p.Phe286Leu)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
14 | g.28768137C= | CA2126000298 | FOXG1 | c.858C= (p.Phe286=)
| |
14 | g.28768137C>G | CA389476014 | FOXG1 | c.858C>G (p.Phe286Leu)
| |
14 | g.28768137C>T | CA486099078 | FOXG1 | c.858C>T (p.Phe286=)
| |
14 | g.28768137dup | CA2695219197 | FOXG1 | c.858dup (p.Lys287GlnfsTer?)
| |
14 | g.28768138A= | CA2126000299 | FOXG1 | c.859A= (p.Lys287=)
| |
14 | g.28768138A>C | CA389476015 | FOXG1 | c.859A>C (p.Lys287Gln)
| |
14 | g.28768138A>G | CA389476017 | FOXG1 | c.859A>G (p.Lys287Glu)
| |
14 | g.28768138A>T | CA389476016 | FOXG1 | c.859A>T (p.Lys287Ter)
| ClinVar dbSNP |
14 | g.28768139A>C | CA389476018 | FOXG1 | c.860A>C (p.Lys287Thr)
| |
14 | g.28768139A>G | CA389476019 | FOXG1 | c.860A>G (p.Lys287Arg)
| |
14 | g.28768139A>T | CA389476020 | FOXG1 | c.860A>T (p.Lys287Met)
| |
14 | g.28768140G>A | CA486099079 | FOXG1 | c.861G>A (p.Lys287=)
| COSMIC |
14 | g.28768140G>C | CA389476021 | FOXG1 | c.861G>C (p.Lys287Asn)
| |
14 | g.28768140G>T | CA389476022 | FOXG1 | c.861G>T (p.Lys287Asn)
| |
14 | g.28768141C>A | CA389476023 | FOXG1 | c.862C>A (p.Arg288Ser)
| dbSNP gnomAD v2 gnomAD v4 |
14 | g.28768141C= | CA2126000300 | FOXG1 | c.862C= (p.Arg288=)
| |
14 | g.28768141C>G | CA389476024 | FOXG1 | c.862C>G (p.Arg288Gly)
| |
14 | g.28768141C>T | CA389476025 | FOXG1 | c.862C>T (p.Arg288Cys)
| |
14 | g.28768142G>A | CA389476026 | FOXG1 | c.863G>A (p.Arg288His)
| COSMIC |
14 | g.28768142G>C | CA389476027 | FOXG1 | c.863G>C (p.Arg288Pro)
| |
14 | g.28768142G>T | CA389476028 | FOXG1 | c.863G>T (p.Arg288Leu)
| |
14 | g.28768143C>A | CA486099080 | FOXG1 | c.864C>A (p.Arg288=)
| ClinVar |
14 | g.28768143C= | CA2126000301 | FOXG1 | c.864C= (p.Arg288=)
| |
14 | g.28768143C>G | CA486099081 | FOXG1 | c.864C>G (p.Arg288=)
| ClinVar dbSNP |
14 | g.28768143C>T | CA486099082 | FOXG1 | c.864C>T (p.Arg288=)
| ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.28768144G>A | CA389476031 | FOXG1 | c.865G>A (p.Gly289Ser)
| COSMIC |
14 | g.28768144G>C | CA389476030 | FOXG1 | c.865G>C (p.Gly289Arg)
| |
14 | g.28768144G>T | CA389476029 | FOXG1 | c.865G>T (p.Gly289Cys)
| gnomAD v4 |
14 | g.28768145G>A | CA389476032 | FOXG1 | c.866G>A (p.Gly289Asp)
| |
14 | g.28768145G>C | CA389476033 | FOXG1 | c.866G>C (p.Gly289Ala)
| |
14 | g.28768145G>T | CA389476034 | FOXG1 | c.866G>T (p.Gly289Val)
| |
14 | g.28768146T>A | CA486099083 | FOXG1 | c.867T>A (p.Gly289=)
| gnomAD v4 |
14 | g.28768146T>C | CA486099084 | FOXG1 | c.867T>C (p.Gly289=)
| |
14 | g.28768146T>G | CA486099085 | FOXG1 | c.867T>G (p.Gly289=)
| gnomAD v4 |
14 | g.28768147G>A | CA389476035 | FOXG1 | c.868G>A (p.Ala290Thr)
| COSMIC |
14 | g.28768147G>C | CA389476036 | FOXG1 | c.868G>C (p.Ala290Pro)
| |
14 | g.28768147G>T | CA389476037 | FOXG1 | c.868G>T (p.Ala290Ser)
| gnomAD v4 |
14 | g.28768148C>A | CA389476038 | FOXG1 | c.869C>A (p.Ala290Glu)
| |
14 | g.28768148C>G | CA389476039 | FOXG1 | c.869C>G (p.Ala290Gly)
| |
14 | g.28768148C>T | CA389476040 | FOXG1 | c.869C>T (p.Ala290Val)
| ClinVar |
14 | g.28768149G>A | CA486099086 | FOXG1 | c.870G>A (p.Ala290=)
| |
14 | g.28768149G>C | CA486099088 | FOXG1 | c.870G>C (p.Ala290=)
| COSMIC |
14 | g.28768149G>T | CA486099087 | FOXG1 | c.870G>T (p.Ala290=)
| gnomAD v4 |
14 | g.28768150C>A | CA389476041 | FOXG1 | c.871C>A (p.Arg291Ser)
| |
14 | g.28768150C>G | CA389476042 | FOXG1 | c.871C>G (p.Arg291Gly)
| |
14 | g.28768150C>T | CA389476043 | FOXG1 | c.871C>T (p.Arg291Cys)
| |
14 | g.28768151G>A | CA389476046 | FOXG1 | c.872G>A (p.Arg291His)
| |
14 | g.28768151G>C | CA389476045 | FOXG1 | c.872G>C (p.Arg291Pro)
| |
14 | g.28768151G>T | CA389476044 | FOXG1 | c.872G>T (p.Arg291Leu)
| gnomAD v4 |
14 | g.28768160_28768174del | CA2624399950 | FOXG1 | c.881_895del (p.Ser294_Thr298del)
| gnomAD v4 |
14 | g.28768152C>A | CA486099089 | FOXG1 | c.873C>A (p.Arg291=)
| |
14 | g.28768152C>G | CA486099090 | FOXG1 | c.873C>G (p.Arg291=)
| |
14 | g.28768152C>T | CA486099091 | FOXG1 | c.873C>T (p.Arg291=)
| |
14 | g.28768153C>A | CA389476047 | FOXG1 | c.874C>A (p.Leu292Ile)
| |
14 | g.28768153C>G | CA389476048 | FOXG1 | c.874C>G (p.Leu292Val)
| gnomAD v4 |
14 | g.28768153C>T | CA389476049 | FOXG1 | c.874C>T (p.Leu292Phe)
| |
14 | g.28768154T>A | CA389476050 | FOXG1 | c.875T>A (p.Leu292His)
| COSMIC |
14 | g.28768154T>C | CA389476051 | FOXG1 | c.875T>C (p.Leu292Pro)
| |
14 | g.28768154T>G | CA389476052 | FOXG1 | c.875T>G (p.Leu292Arg)
| |
14 | g.28768155C>A | CA486098208 | FOXG1 | c.876C>A (p.Leu292=)
| |
14 | g.28768155C= | CA2126000302 | FOXG1 | c.876C= (p.Leu292=)
| |
14 | g.28768155C>G | CA486098210 | FOXG1 | c.876C>G (p.Leu292=)
| ClinVar |
14 | g.28768155C>T | CA486098209 | FOXG1 | c.876C>T (p.Leu292=)
| dbSNP gnomAD v2 |
14 | g.28768156A= | CA2126000303 | FOXG1 | c.877A= (p.Thr293=)
| |
14 | g.28768156A>C | CA258396583 | FOXG1 | c.877A>C (p.Thr293Pro)
| dbSNP |
14 | g.28768156A>G | CA389476053 | FOXG1 | c.877A>G (p.Thr293Ala)
| gnomAD v4 |
14 | g.28768156A>T | CA389476054 | FOXG1 | c.877A>T (p.Thr293Ser)
| |
14 | g.28768157C>A | CA389476055 | FOXG1 | c.878C>A (p.Thr293Asn)
| |
14 | g.28768157C>G | CA389476056 | FOXG1 | c.878C>G (p.Thr293Ser)
| |
14 | g.28768157C>T | CA389476057 | FOXG1 | c.878C>T (p.Thr293Ile)
| |
14 | g.28768158C>A | CA486098214 | FOXG1 | c.879C>A (p.Thr293=)
| gnomAD v4 |
14 | g.28768158C= | CA2126000304 | FOXG1 | c.879C= (p.Thr293=)
| |
14 | g.28768158C>G | CA486098215 | FOXG1 | c.879C>G (p.Thr293=)
| dbSNP gnomAD v2 gnomAD v4 |
14 | g.28768158C>T | CA486098216 | FOXG1 | c.879C>T (p.Thr293=)
| gnomAD v4 |
14 | g.28768159T>A | CA389476059 | FOXG1 | c.880T>A (p.Ser294Thr)
| |
14 | g.28768159T>C | CA314628 | FOXG1 | c.880T>C (p.Ser294Pro)
| ClinVar dbSNP |
14 | g.28768159T>G | CA389476058 | FOXG1 | c.880T>G (p.Ser294Ala)
| |
14 | g.28768159T= | CA2126000305 | FOXG1 | c.880T= (p.Ser294=)
| |
14 | g.28768160C>A | CA389476060 | FOXG1 | c.881C>A (p.Ser294Tyr)
| COSMIC |
14 | g.28768160C>G | CA389476061 | FOXG1 | c.881C>G (p.Ser294Cys)
| |
14 | g.28768160C>T | CA389476062 | FOXG1 | c.881C>T (p.Ser294Phe)
| |
14 | g.28768161C>A | CA486098221 | FOXG1 | c.882C>A (p.Ser294=)
| |
14 | g.28768161C>G | CA486098222 | FOXG1 | c.882C>G (p.Ser294=)
| |
14 | g.28768161C>T | CA486098223 | FOXG1 | c.882C>T (p.Ser294=)
| gnomAD v4 |
14 | g.28768162A= | CA2126000306 | FOXG1 | c.883A= (p.Thr295=)
| |
14 | g.28768162A>C | CA389476063 | FOXG1 | c.883A>C (p.Thr295Pro)
| |
14 | g.28768162A>G | CA389476064 | FOXG1 | c.883A>G (p.Thr295Ala)
| |
14 | g.28768162A>T | CA389476065 | FOXG1 | c.883A>T (p.Thr295Ser)
| |
14 | g.28768163C>A | CA389476066 | FOXG1 | c.884C>A (p.Thr295Asn)
| |
14 | g.28768163C>G | CA389476067 | FOXG1 | c.884C>G (p.Thr295Ser)
| |
14 | g.28768163C>T | CA389476068 | FOXG1 | c.884C>T (p.Thr295Ile)
| |
14 | g.28768164dup | CA16043741 | FOXG1 | c.885dup (p.Gly296ArgfsTer?)
| ClinVar dbSNP |
14 | g.28768164C>A | CA486098226 | FOXG1 | c.885C>A (p.Thr295=)
| dbSNP gnomAD v3 gnomAD v4 |
14 | g.28768164C= | CA2126000307 | FOXG1 | c.885C= (p.Thr295=)
| |
14 | g.28768164C>G | CA486098225 | FOXG1 | c.885C>G (p.Thr295=)
| gnomAD v4 |
14 | g.28768164C>T | CA7140637 | FOXG1 | c.885C>T (p.Thr295=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.28768165G>A | CA389476069 | FOXG1 | c.886G>A (p.Gly296Ser)
| ClinVar gnomAD v4 |
14 | g.28768165G>C | CA389476070 | FOXG1 | c.886G>C (p.Gly296Arg)
| |
14 | g.28768165G>T | CA389476071 | FOXG1 | c.886G>T (p.Gly296Cys)
| |
14 | g.28768166del | CA2840770144 | FOXG1 | c.887del (p.Gly296AlafsTer30)
| |
14 | g.28768166G>A | CA389476074 | FOXG1 | c.887G>A (p.Gly296Asp)
| |
14 | g.28768166G>C | CA389476073 | FOXG1 | c.887G>C (p.Gly296Ala)
| |
14 | g.28768166G= | CA2126000308 | FOXG1 | c.887G= (p.Gly296=)
| |
14 | g.28768166G>T | CA389476072 | FOXG1 | c.887G>T (p.Gly296Val)
| ClinVar dbSNP |
14 | g.28768167C>A | CA486098231 | FOXG1 | c.888C>A (p.Gly296=)
| |
14 | g.28768167C>G | CA486098232 | FOXG1 | c.888C>G (p.Gly296=)
| |
14 | g.28768167C>T | CA486098233 | FOXG1 | c.888C>T (p.Gly296=)
| |
14 | g.28768168C>A | CA389476076 | FOXG1 | c.889C>A (p.Leu297Ile)
| COSMIC |
14 | g.28768168C>G | CA389476075 | FOXG1 | c.889C>G (p.Leu297Val)
| |
14 | g.28768168C>T | CA389476077 | FOXG1 | c.889C>T (p.Leu297Phe)
| gnomAD v4 |
14 | g.28768169T>A | CA389476078 | FOXG1 | c.890T>A (p.Leu297His)
| COSMIC |
14 | g.28768169T>C | CA389476079 | FOXG1 | c.890T>C (p.Leu297Pro)
| |
14 | g.28768169T>G | CA389476080 | FOXG1 | c.890T>G (p.Leu297Arg)
| |
14 | g.28768170C>A | CA486098236 | FOXG1 | c.891C>A (p.Leu297=)
| |
14 | g.28768170C= | CA2126000309 | FOXG1 | c.891C= (p.Leu297=)
| |
14 | g.28768170C>G | CA486098234 | FOXG1 | c.891C>G (p.Leu297=)
| COSMIC |
14 | g.28768170C>T | CA486098238 | FOXG1 | c.891C>T (p.Leu297=)
| dbSNP gnomAD v2 gnomAD v4 |
14 | g.28768171A>C | CA389476081 | FOXG1 | c.892A>C (p.Thr298Pro)
| |
14 | g.28768171A>G | CA389476082 | FOXG1 | c.892A>G (p.Thr298Ala)
| |
14 | g.28768171A>T | CA389476083 | FOXG1 | c.892A>T (p.Thr298Ser)
| |
14 | g.28768172C>A | CA389476084 | FOXG1 | c.893C>A (p.Thr298Asn)
| |
14 | g.28768172C>G | CA389476085 | FOXG1 | c.893C>G (p.Thr298Ser)
| ClinVar dbSNP |
14 | g.28768172C>T | CA389476086 | FOXG1 | c.893C>T (p.Thr298Ile)
| |
14 | g.28768173C>A | CA486098240 | FOXG1 | c.894C>A (p.Thr298=)
| |
14 | g.28768173C= | CA2126000310 | FOXG1 | c.894C= (p.Thr298=)
| |
14 | g.28768173C>G | CA486098241 | FOXG1 | c.894C>G (p.Thr298=)
| dbSNP gnomAD v2 gnomAD v4 |
14 | g.28768173C>T | CA486098242 | FOXG1 | c.894C>T (p.Thr298=)
| gnomAD v4 |
14 | g.28768174T>A | CA389476087 | FOXG1 | c.895T>A (p.Phe299Ile)
| |
14 | g.28768174T>C | CA389476088 | FOXG1 | c.895T>C (p.Phe299Leu)
| |
14 | g.28768174T>G | CA389476089 | FOXG1 | c.895T>G (p.Phe299Val)
| |
14 | g.28768175T>A | CA389476092 | FOXG1 | c.896T>A (p.Phe299Tyr)
| |
14 | g.28768175T>C | CA389476090 | FOXG1 | c.896T>C (p.Phe299Ser)
| |
14 | g.28768175T>G | CA389476091 | FOXG1 | c.896T>G (p.Phe299Cys)
| |
14 | g.28768176C>A | CA389476093 | FOXG1 | c.897C>A (p.Phe299Leu)
| |
14 | g.28768176C= | CA2126000311 | FOXG1 | c.897C= (p.Phe299=)
| |
14 | g.28768176C>G | CA389476094 | FOXG1 | c.897C>G (p.Phe299Leu)
| |
14 | g.28768176C>T | CA486098247 | FOXG1 | c.897C>T (p.Phe299=)
| dbSNP gnomAD v2 COSMIC |
14 | g.28768177A>C | CA389476095 | FOXG1 | c.898A>C (p.Met300Leu)
| |
14 | g.28768177A>G | CA389476096 | FOXG1 | c.898A>G (p.Met300Val)
| gnomAD v4 |
14 | g.28768177A>T | CA389476097 | FOXG1 | c.898A>T (p.Met300Leu)
| |
14 | g.28768178T>A | CA389476098 | FOXG1 | c.899T>A (p.Met300Lys)
| gnomAD v3 gnomAD v4 |
14 | g.28768178T>C | CA389476099 | FOXG1 | c.899T>C (p.Met300Thr)
| |
14 | g.28768178T>G | CA389476100 | FOXG1 | c.899T>G (p.Met300Arg)
| |