14 | g.28767412_28767748delinsACCCACCGCCCC | CA2766230034 | FOXG1 | c.133_469delinsACCCACCGCCCC (p.Pro45ThrfsTer?)
| |
14 | g.28767517_28767625del | CA2801003621 | FOXG1 | c.238_346del (p.Pro80TrpfsTer?)
| |
14 | g.28767603_28767624del | CA2624398855 | FOXG1 | c.324_345del (p.Pro109TrpfsTer?)
| gnomAD v4 |
14 | g.28767615_28767624del | CA1139663424 | FOXG1 | c.336_345del (p.Ala113TrpfsTer?)
| ClinVar |
14 | g.28767620_28767631del | CA2624398965 | FOXG1 | c.341_352del (p.Ala114_Asp117del)
| gnomAD v4 |
14 | g.28767622G>A | CA389474901 | FOXG1 | c.343G>A (p.Ala115Thr)
| gnomAD v4 |
14 | g.28767622G>C | CA389474902 | FOXG1 | c.343G>C (p.Ala115Pro)
| |
14 | g.28767622G>T | CA389474903 | FOXG1 | c.343G>T (p.Ala115Ser)
| gnomAD v4 |
14 | g.28767623C>A | CA389474904 | FOXG1 | c.344C>A (p.Ala115Asp)
| gnomAD v4 |
14 | g.28767623C= | CA2125999201 | FOXG1 | c.344C= (p.Ala115=)
| |
14 | g.28767623C>G | CA258396560 | FOXG1 | c.344C>G (p.Ala115Gly)
| dbSNP |
14 | g.28767623C>T | CA314580 | FOXG1 | c.344C>T (p.Ala115Val)
| ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.28767624C>A | CA486098290 | FOXG1 | c.345C>A (p.Ala115=)
| |
14 | g.28767624C>G | CA486098291 | FOXG1 | c.345C>G (p.Ala115=)
| |
14 | g.28767624C>T | CA486098292 | FOXG1 | c.345C>T (p.Ala115=)
| gnomAD v4 |
14 | g.28767625C>A | CA389474906 | FOXG1 | c.346C>A (p.Leu116Met)
| gnomAD v4 |
14 | g.28767625C>G | CA389474905 | FOXG1 | c.346C>G (p.Leu116Val)
| |
14 | g.28767625C>T | CA486098294 | FOXG1 | c.346C>T (p.Leu116=)
| |
14 | g.28767626T>A | CA389474907 | FOXG1 | c.347T>A (p.Leu116Gln)
| gnomAD v4 |
14 | g.28767626T>C | CA389474908 | FOXG1 | c.347T>C (p.Leu116Pro)
| ClinVar dbSNP gnomAD v4 |
14 | g.28767626T>G | CA389474909 | FOXG1 | c.347T>G (p.Leu116Arg)
| ClinVar |
14 | g.28767626T= | CA2125999207 | FOXG1 | c.347T= (p.Leu116=)
| |
14 | g.28767627G>A | CA486098295 | FOXG1 | c.348G>A (p.Leu116=)
| gnomAD v4 |
14 | g.28767627G>C | CA486098296 | FOXG1 | c.348G>C (p.Leu116=)
| |
14 | g.28767627G>T | CA486098297 | FOXG1 | c.348G>T (p.Leu116=)
| gnomAD v4 |
14 | g.28767634_28767648del | CA2624398994 | FOXG1 | c.355_369del (p.Ala119_Gly123del)
| gnomAD v4 |
14 | g.28767628G>A | CA389474910 | FOXG1 | c.349G>A (p.Asp117Asn)
| dbSNP gnomAD v2 gnomAD v4 |
14 | g.28767628G>C | CA389474911 | FOXG1 | c.349G>C (p.Asp117His)
| |
14 | g.28767628G= | CA2125999211 | FOXG1 | c.349G= (p.Asp117=)
| |
14 | g.28767628G>T | CA389474912 | FOXG1 | c.349G>T (p.Asp117Tyr)
| gnomAD v4 |
14 | g.28767629A>C | CA389474913 | FOXG1 | c.350A>C (p.Asp117Ala)
| |
14 | g.28767629A>G | CA389474915 | FOXG1 | c.350A>G (p.Asp117Gly)
| ClinVar |
14 | g.28767629A>T | CA389474914 | FOXG1 | c.350A>T (p.Asp117Val)
| |
14 | g.28767630C>A | CA389474916 | FOXG1 | c.351C>A (p.Asp117Glu)
| gnomAD v4 |
14 | g.28767630C>G | CA389474917 | FOXG1 | c.351C>G (p.Asp117Glu)
| |
14 | g.28767630C>T | CA486098301 | FOXG1 | c.351C>T (p.Asp117=)
| ClinVar dbSNP gnomAD v4 |
14 | g.28767631G>A | CA389474918 | FOXG1 | c.352G>A (p.Gly118Arg)
| ClinVar dbSNP gnomAD v2 gnomAD v4 |
14 | g.28767631G>C | CA389474919 | FOXG1 | c.352G>C (p.Gly118Arg)
| gnomAD v4 |
14 | g.28767631G= | CA2125999214 | FOXG1 | c.352G= (p.Gly118=)
| |
14 | g.28767631G>T | CA389474920 | FOXG1 | c.352G>T (p.Gly118Trp)
| gnomAD v4 |
14 | g.28767632G>A | CA389474921 | FOXG1 | c.353G>A (p.Gly118Glu)
| gnomAD v4 |
14 | g.28767632G>C | CA389474922 | FOXG1 | c.353G>C (p.Gly118Ala)
| |
14 | g.28767632G>T | CA389474923 | FOXG1 | c.353G>T (p.Gly118Val)
| gnomAD v4 |
14 | g.28767633G>A | CA486098305 | FOXG1 | c.354G>A (p.Gly118=)
| dbSNP gnomAD v2 gnomAD v4 |
14 | g.28767633G>C | CA486098306 | FOXG1 | c.354G>C (p.Gly118=)
| ClinVar gnomAD v4 |
14 | g.28767633G= | CA2125999217 | FOXG1 | c.354G= (p.Gly118=)
| |
14 | g.28767633G>T | CA486098307 | FOXG1 | c.354G>T (p.Gly118=)
| |
14 | g.28767634G>A | CA389474924 | FOXG1 | c.355G>A (p.Ala119Thr)
| gnomAD v4 |
14 | g.28767634G>C | CA389474925 | FOXG1 | c.355G>C (p.Ala119Pro)
| |
14 | g.28767634G= | CA2125999220 | FOXG1 | c.355G= (p.Ala119=)
| |
14 | g.28767634G>T | CA314602 | FOXG1 | c.355G>T (p.Ala119Ser)
| ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.28767635del | CA2573149900 | FOXG1 | c.356del (p.Ala119ValfsTer?)
| ClinVar dbSNP |
14 | g.28767635C>A | CA389474926 | FOXG1 | c.356C>A (p.Ala119Asp)
| gnomAD v4 |
14 | g.28767635C>G | CA389474928 | FOXG1 | c.356C>G (p.Ala119Gly)
| |
14 | g.28767635C>T | CA389474927 | FOXG1 | c.356C>T (p.Ala119Val)
| gnomAD v4 |
14 | g.28767636T>A | CA486098311 | FOXG1 | c.357T>A (p.Ala119=)
| |
14 | g.28767636T>C | CA486098312 | FOXG1 | c.357T>C (p.Ala119=)
| |
14 | g.28767636T>G | CA486098313 | FOXG1 | c.357T>G (p.Ala119=)
| dbSNP |
14 | g.28767636T= | CA2125999222 | FOXG1 | c.357T= (p.Ala119=)
| |
14 | g.28767637A>C | CA389474929 | FOXG1 | c.358A>C (p.Lys120Gln)
| |
14 | g.28767637A>G | CA389474931 | FOXG1 | c.358A>G (p.Lys120Glu)
| |
14 | g.28767637A>T | CA389474930 | FOXG1 | c.358A>T (p.Lys120Ter)
| |
14 | g.28767639del | CA2624399018 | FOXG1 | c.360del (p.Ala121ArgfsTer?)
| gnomAD v4 |
14 | g.28767638A= | CA2125999224 | FOXG1 | c.359A= (p.Lys120=)
| |
14 | g.28767638A>C | CA389474932 | FOXG1 | c.359A>C (p.Lys120Thr)
| |
14 | g.28767638A>G | CA389474933 | FOXG1 | c.359A>G (p.Lys120Arg)
| |
14 | g.28767638A>T | CA389474934 | FOXG1 | c.359A>T (p.Lys120Ile)
| dbSNP gnomAD v2 gnomAD v4 |
14 | g.28767639A>C | CA389474935 | FOXG1 | c.360A>C (p.Lys120Asn)
| |
14 | g.28767639A>G | CA486098319 | FOXG1 | c.360A>G (p.Lys120=)
| gnomAD v4 |
14 | g.28767639A>T | CA389474936 | FOXG1 | c.360A>T (p.Lys120Asn)
| |
14 | g.28767640G>A | CA389474937 | FOXG1 | c.361G>A (p.Ala121Thr)
| |
14 | g.28767640G>C | CA389474938 | FOXG1 | c.361G>C (p.Ala121Pro)
| ClinVar dbSNP gnomAD v4 |
14 | g.28767640G= | CA2125999227 | FOXG1 | c.361G= (p.Ala121=)
| |
14 | g.28767640G>T | CA389474939 | FOXG1 | c.361G>T (p.Ala121Ser)
| dbSNP |
14 | g.28767641C>A | CA389474940 | FOXG1 | c.362C>A (p.Ala121Glu)
| gnomAD v4 |
14 | g.28767641C>G | CA389474941 | FOXG1 | c.362C>G (p.Ala121Gly)
| ClinVar dbSNP |
14 | g.28767641C>T | CA389474942 | FOXG1 | c.362C>T (p.Ala121Val)
| gnomAD v4 |
14 | g.28767642G>A | CA486098330 | FOXG1 | c.363G>A (p.Ala121=)
| dbSNP gnomAD v3 gnomAD v4 |
14 | g.28767642G>C | CA486098327 | FOXG1 | c.363G>C (p.Ala121=)
| dbSNP gnomAD v4 |
14 | g.28767642G= | CA2125999229 | FOXG1 | c.363G= (p.Ala121=)
| |
14 | g.28767642G>T | CA486098325 | FOXG1 | c.363G>T (p.Ala121=)
| |
14 | g.28767643G>A | CA389474945 | FOXG1 | c.364G>A (p.Asp122Asn)
| |
14 | g.28767643G>C | CA389474943 | FOXG1 | c.364G>C (p.Asp122His)
| |
14 | g.28767643G>T | CA389474944 | FOXG1 | c.364G>T (p.Asp122Tyr)
| |
14 | g.28767644A>C | CA389474946 | FOXG1 | c.365A>C (p.Asp122Ala)
| gnomAD v4 |
14 | g.28767644A>G | CA389474947 | FOXG1 | c.365A>G (p.Asp122Gly)
| |
14 | g.28767644A>T | CA389474948 | FOXG1 | c.365A>T (p.Asp122Val)
| |
14 | g.28767645C>A | CA389474949 | FOXG1 | c.366C>A (p.Asp122Glu)
| dbSNP gnomAD v3 gnomAD v4 |
14 | g.28767645C= | CA2125999231 | FOXG1 | c.366C= (p.Asp122=)
| |
14 | g.28767645C>G | CA389474950 | FOXG1 | c.366C>G (p.Asp122Glu)
| |
14 | g.28767645C>T | CA486098095 | FOXG1 | c.366C>T (p.Asp122=)
| gnomAD v4 |
14 | g.28767646G>A | CA258396561 | FOXG1 | c.367G>A (p.Gly123Arg)
| ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.28767646G>C | CA7140595 | FOXG1 | c.367G>C (p.Gly123Arg)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.28767646G= | CA2125999233 | FOXG1 | c.367G= (p.Gly123=)
| |
14 | g.28767646G>T | CA389474951 | FOXG1 | c.367G>T (p.Gly123Trp)
| |
14 | g.28767647G>A | CA389474952 | FOXG1 | c.368G>A (p.Gly123Glu)
| |
14 | g.28767647G>C | CA389474953 | FOXG1 | c.368G>C (p.Gly123Ala)
| |
14 | g.28767647G>T | CA389474954 | FOXG1 | c.368G>T (p.Gly123Val)
| gnomAD v4 |
14 | g.28767648G>A | CA486098099 | FOXG1 | c.369G>A (p.Gly123=)
| gnomAD v4 |
14 | g.28767648G>C | CA486098100 | FOXG1 | c.369G>C (p.Gly123=)
| |
14 | g.28767648G>T | CA486098102 | FOXG1 | c.369G>T (p.Gly123=)
| gnomAD v4 |
14 | g.28767649C>A | CA389474956 | FOXG1 | c.370C>A (p.Leu124Met)
| |
14 | g.28767649C>G | CA389474955 | FOXG1 | c.370C>G (p.Leu124Val)
| |
14 | g.28767649C>T | CA486098105 | FOXG1 | c.370C>T (p.Leu124=)
| gnomAD v4 |
14 | g.28767650T>A | CA389474957 | FOXG1 | c.371T>A (p.Leu124Gln)
| gnomAD v4 |
14 | g.28767650T>C | CA389474958 | FOXG1 | c.371T>C (p.Leu124Pro)
| COSMIC |
14 | g.28767650T>G | CA389474959 | FOXG1 | c.371T>G (p.Leu124Arg)
| |
14 | g.28767650_28767668delinsTGGGCGGCAAGGGCGAGCC | CA2125999237 | FOXG1 | c.371_389delinsTGGGCGGCAAGGGCGAGCC (p.Leu124=)
| |
14 | g.28767651G>A | CA486098106 | FOXG1 | c.372G>A (p.Leu124=)
| |
14 | g.28767651G>C | CA486098107 | FOXG1 | c.372G>C (p.Leu124=)
| |
14 | g.28767651G>T | CA486098108 | FOXG1 | c.372G>T (p.Leu124=)
| COSMIC |
14 | g.28767658_28767675dup | CA2624399050 | FOXG1 | c.379_396dup (p.Gly132_Gly133insLysGlyGluProGlyGly)
| gnomAD v4 |
14 | g.28767658_28767675del | CA2125999239 | FOXG1 | c.379_396del (p.Lys127_Gly132del)
| ClinVar dbSNP gnomAD v4 |
14 | g.28767662_28767772del | CA2624399051 | FOXG1 | c.383_493del (p.Gly128_Lys164del)
| gnomAD v4 |
14 | g.28767652G>A | CA389474960 | FOXG1 | c.373G>A (p.Gly125Ser)
| |
14 | g.28767652G>C | CA389474961 | FOXG1 | c.373G>C (p.Gly125Arg)
| |
14 | g.28767652G>T | CA389474962 | FOXG1 | c.373G>T (p.Gly125Cys)
| |
14 | g.28767653G>A | CA389474963 | FOXG1 | c.374G>A (p.Gly125Asp)
| |
14 | g.28767653G>C | CA389474964 | FOXG1 | c.374G>C (p.Gly125Ala)
| |
14 | g.28767653G>T | CA389474965 | FOXG1 | c.374G>T (p.Gly125Val)
| |
14 | g.28767654C>A | CA486098110 | FOXG1 | c.375C>A (p.Gly125=)
| ClinVar dbSNP |
14 | g.28767654C= | CA2125999242 | FOXG1 | c.375C= (p.Gly125=)
| |
14 | g.28767654C>G | CA486098111 | FOXG1 | c.375C>G (p.Gly125=)
| |
14 | g.28767654C>T | CA486098112 | FOXG1 | c.375C>T (p.Gly125=)
| dbSNP gnomAD v2 gnomAD v4 |
14 | g.28767655G>A | CA314582 | FOXG1 | c.376G>A (p.Gly126Ser)
| ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.28767655G>C | CA389474966 | FOXG1 | c.376G>C (p.Gly126Arg)
| |
14 | g.28767655G= | CA2125999245 | FOXG1 | c.376G= (p.Gly126=)
| |
14 | g.28767655G>T | CA389474967 | FOXG1 | c.376G>T (p.Gly126Cys)
| |
14 | g.28767656G>A | CA389474970 | FOXG1 | c.377G>A (p.Gly126Asp)
| dbSNP gnomAD v4 |
14 | g.28767656G>C | CA389474969 | FOXG1 | c.377G>C (p.Gly126Ala)
| |
14 | g.28767656G= | CA2125999249 | FOXG1 | c.377G= (p.Gly126=)
| |
14 | g.28767656G>T | CA389474968 | FOXG1 | c.377G>T (p.Gly126Val)
| gnomAD v4 |
14 | g.28767657C>A | CA486098113 | FOXG1 | c.378C>A (p.Gly126=)
| |
14 | g.28767657C= | CA2125999255 | FOXG1 | c.378C= (p.Gly126=)
| |
14 | g.28767657C>G | CA486098114 | FOXG1 | c.378C>G (p.Gly126=)
| |
14 | g.28767657C>T | CA258396562 | FOXG1 | c.378C>T (p.Gly126=)
| ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.28767658A>C | CA389474971 | FOXG1 | c.379A>C (p.Lys127Gln)
| |
14 | g.28767658A>G | CA389474972 | FOXG1 | c.379A>G (p.Lys127Glu)
| ClinVar |
14 | g.28767658A>T | CA389474973 | FOXG1 | c.379A>T (p.Lys127Ter)
| |
14 | g.28767659A= | CA2125999266 | FOXG1 | c.380A= (p.Lys127=)
| |
14 | g.28767659A>C | CA389474974 | FOXG1 | c.380A>C (p.Lys127Thr)
| |
14 | g.28767659A>G | CA258396563 | FOXG1 | c.380A>G (p.Lys127Arg)
| dbSNP |
14 | g.28767659A>T | CA389474975 | FOXG1 | c.380A>T (p.Lys127Met)
| |
14 | g.28767660G>A | CA486098119 | FOXG1 | c.381G>A (p.Lys127=)
| dbSNP gnomAD v3 gnomAD v4 |
14 | g.28767660G>C | CA389474976 | FOXG1 | c.381G>C (p.Lys127Asn)
| gnomAD v4 |
14 | g.28767660G= | CA2125999273 | FOXG1 | c.381G= (p.Lys127=)
| |
14 | g.28767660G>T | CA389474977 | FOXG1 | c.381G>T (p.Lys127Asn)
| |
14 | g.28767662dup | CA314640 | FOXG1 | c.383dup (p.Glu129ArgfsTer?)
| ClinVar dbSNP |
14 | g.28767661G>A | CA389474978 | FOXG1 | c.382G>A (p.Gly128Ser)
| gnomAD v4 |
14 | g.28767661G>C | CA389474979 | FOXG1 | c.382G>C (p.Gly128Arg)
| |
14 | g.28767661G= | CA2125999280 | FOXG1 | c.382G= (p.Gly128=)
| |
14 | g.28767661G>T | CA258396564 | FOXG1 | c.382G>T (p.Gly128Cys)
| ClinVar dbSNP gnomAD v3 gnomAD v4 |
14 | g.28767665_28767676dup | CA314584 | FOXG1 | c.386_397dup (p.Gly132_Gly133insGluProGlyGly)
| ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.28767662G>A | CA389474982 | FOXG1 | c.383G>A (p.Gly128Asp)
| dbSNP |
14 | g.28767662G>C | CA389474981 | FOXG1 | c.383G>C (p.Gly128Ala)
| |
14 | g.28767662G= | CA2125999285 | FOXG1 | c.383G= (p.Gly128=)
| |
14 | g.28767662G>T | CA389474980 | FOXG1 | c.383G>T (p.Gly128Val)
| |
14 | g.28767663C>A | CA486098124 | FOXG1 | c.384C>A (p.Gly128=)
| gnomAD v4 |
14 | g.28767663C= | CA2125999287 | FOXG1 | c.384C= (p.Gly128=)
| |
14 | g.28767663C>G | CA258396565 | FOXG1 | c.384C>G (p.Gly128=)
| dbSNP gnomAD v4 |
14 | g.28767663C>T | CA486098123 | FOXG1 | c.384C>T (p.Gly128=)
| gnomAD v4 |
14 | g.28767664del | CA2573053890 | FOXG1 | c.385del (p.Glu129SerfsTer?)
| ClinVar dbSNP |
14 | g.28767664G>A | CA389474983 | FOXG1 | c.385G>A (p.Glu129Lys)
| |
14 | g.28767664G>C | CA389474985 | FOXG1 | c.385G>C (p.Glu129Gln)
| |
14 | g.28767664G= | CA2125999292 | FOXG1 | c.385G= (p.Glu129=)
| |
14 | g.28767664G>T | CA389474984 | FOXG1 | c.385G>T (p.Glu129Ter)
| ClinVar dbSNP |
14 | g.28767665A>C | CA389474986 | FOXG1 | c.386A>C (p.Glu129Ala)
| |
14 | g.28767665A>G | CA389474987 | FOXG1 | c.386A>G (p.Glu129Gly)
| |
14 | g.28767665A>T | CA389474988 | FOXG1 | c.386A>T (p.Glu129Val)
| |
14 | g.28767666G>A | CA486098126 | FOXG1 | c.387G>A (p.Glu129=)
| |
14 | g.28767666G>C | CA389474989 | FOXG1 | c.387G>C (p.Glu129Asp)
| |
14 | g.28767666G>T | CA389474990 | FOXG1 | c.387G>T (p.Glu129Asp)
| |
14 | g.28767667C>A | CA389474991 | FOXG1 | c.388C>A (p.Pro130Thr)
| gnomAD v4 |
14 | g.28767667C>G | CA389474992 | FOXG1 | c.388C>G (p.Pro130Ala)
| |
14 | g.28767667C>T | CA389474993 | FOXG1 | c.388C>T (p.Pro130Ser)
| gnomAD v4 |
14 | g.28767668del | CA2580087997 | FOXG1 | c.389del (p.Pro130ArgfsTer?)
| ClinVar |
14 | g.28767668C>A | CA389474994 | FOXG1 | c.389C>A (p.Pro130Gln)
| gnomAD v4 |
14 | g.28767668C>G | CA389474995 | FOXG1 | c.389C>G (p.Pro130Arg)
| gnomAD v4 |
14 | g.28767668C>T | CA389474996 | FOXG1 | c.389C>T (p.Pro130Leu)
| gnomAD v4 |
14 | g.28767669G>A | CA258396566 | FOXG1 | c.390G>A (p.Pro130=)
| ClinVar dbSNP gnomAD v3 gnomAD v4 |
14 | g.28767669G>C | CA486098128 | FOXG1 | c.390G>C (p.Pro130=)
| |
14 | g.28767669G= | CA2125999295 | FOXG1 | c.390G= (p.Pro130=)
| |
14 | g.28767669G>T | CA486098129 | FOXG1 | c.390G>T (p.Pro130=)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.28767671del | CA2695219190 | FOXG1 | c.392del (p.Gly131AlafsTer?)
| |
14 | g.28767670G>A | CA389474997 | FOXG1 | c.391G>A (p.Gly131Ser)
| gnomAD v4 |
14 | g.28767670G>C | CA389474998 | FOXG1 | c.391G>C (p.Gly131Arg)
| |
14 | g.28767670G>T | CA389474999 | FOXG1 | c.391G>T (p.Gly131Cys)
| |
14 | g.28767671G>A | CA389475000 | FOXG1 | c.392G>A (p.Gly131Asp)
| |
14 | g.28767671G>C | CA389475002 | FOXG1 | c.392G>C (p.Gly131Ala)
| ClinVar gnomAD v4 |
14 | g.28767671G>T | CA389475001 | FOXG1 | c.392G>T (p.Gly131Val)
| ClinVar gnomAD v4 |
14 | g.28767672_28767673del | CA2624399060 | FOXG1 | c.393_394del (p.Gly132ArgfsTer?)
| gnomAD v4 |
14 | g.28767672C>A | CA486098133 | FOXG1 | c.393C>A (p.Gly131=)
| |
14 | g.28767672C= | CA2125999297 | FOXG1 | c.393C= (p.Gly131=)
| |
14 | g.28767672C>G | CA486098134 | FOXG1 | c.393C>G (p.Gly131=)
| dbSNP |
14 | g.28767672C>T | CA486098135 | FOXG1 | c.393C>T (p.Gly131=)
| dbSNP gnomAD v4 |
14 | g.28767673G>A | CA389475003 | FOXG1 | c.394G>A (p.Gly132Ser)
| ClinVar dbSNP |
14 | g.28767673G>C | CA389475004 | FOXG1 | c.394G>C (p.Gly132Arg)
| |
14 | g.28767673G= | CA2125999303 | FOXG1 | c.394G= (p.Gly132=)
| |
14 | g.28767673G>T | CA389475005 | FOXG1 | c.394G>T (p.Gly132Cys)
| dbSNP gnomAD v4 |
14 | g.28767674G>A | CA389475006 | FOXG1 | c.395G>A (p.Gly132Asp)
| |
14 | g.28767674G>C | CA389475007 | FOXG1 | c.395G>C (p.Gly132Ala)
| |
14 | g.28767674G>T | CA389475008 | FOXG1 | c.395G>T (p.Gly132Val)
| |
14 | g.28767675C>A | CA486098136 | FOXG1 | c.396C>A (p.Gly132=)
| gnomAD v4 |
14 | g.28767675C>G | CA486098137 | FOXG1 | c.396C>G (p.Gly132=)
| |
14 | g.28767675C>T | CA486098139 | FOXG1 | c.396C>T (p.Gly132=)
| gnomAD v4 |
14 | g.28767675_28767676delinsCG | CA2125999307 | FOXG1 | c.396_397delinsCG (p.Gly132=)
| |
14 | g.28767676G>A | CA389475009 | FOXG1 | c.397G>A (p.Gly133Arg)
| |
14 | g.28767676G>C | CA389475010 | FOXG1 | c.397G>C (p.Gly133Arg)
| ClinVar dbSNP gnomAD v4 |
14 | g.28767676G>T | CA389475011 | FOXG1 | c.397G>T (p.Gly133Trp)
| |
14 | g.28767678del | CA314641 | FOXG1 | c.399del (p.Pro134ArgfsTer?)
| ClinVar dbSNP gnomAD v4 |
14 | g.28767677G>A | CA389475013 | FOXG1 | c.398G>A (p.Gly133Glu)
| ClinVar |
14 | g.28767677G>C | CA389475014 | FOXG1 | c.398G>C (p.Gly133Ala)
| |
14 | g.28767677G>T | CA389475012 | FOXG1 | c.398G>T (p.Gly133Val)
| |
14 | g.28767677_28767729delinsGGCCGGGGGAGCTGGCGCCCGTCGGGCCGGACGAGAAGGAGAAGGGCGCCGGC | CA2125999315 | FOXG1 | c.398_450delinsGGCCGGGGGAGCTGGCGCCCGTCGGGCCGGACGAGAAGGAGAAGGGCGCCGGC (p.Gly133=)
| |
14 | g.28767678G>A | CA486098142 | FOXG1 | c.399G>A (p.Gly133=)
| |
14 | g.28767678G>C | CA486098143 | FOXG1 | c.399G>C (p.Gly133=)
| |
14 | g.28767678G>T | CA486098144 | FOXG1 | c.399G>T (p.Gly133=)
| |
14 | g.28767686_28767737del | CA891844335 | FOXG1 | c.407_458del (p.Glu136GlyfsTer?)
| ClinVar dbSNP |
14 | g.28767679C>A | CA389475015 | FOXG1 | c.400C>A (p.Pro134Thr)
| |
14 | g.28767679C= | CA2125999320 | FOXG1 | c.400C= (p.Pro134=)
| |
14 | g.28767679C>G | CA389475016 | FOXG1 | c.400C>G (p.Pro134Ala)
| |
14 | g.28767679C>T | CA389475017 | FOXG1 | c.400C>T (p.Pro134Ser)
| ClinVar dbSNP gnomAD v4 |
14 | g.28767680C>A | CA389475018 | FOXG1 | c.401C>A (p.Pro134Gln)
| gnomAD v4 |
14 | g.28767680C>G | CA389475019 | FOXG1 | c.401C>G (p.Pro134Arg)
| ClinVar dbSNP gnomAD v4 |
14 | g.28767680C>T | CA389475020 | FOXG1 | c.401C>T (p.Pro134Leu)
| gnomAD v4 |
14 | g.28767680_28767681delinsCG | CA2125999325 | FOXG1 | c.401_402delinsCG (p.Pro134=)
| |
14 | g.28767681G>A | CA486098150 | FOXG1 | c.402G>A (p.Pro134=)
| ClinVar dbSNP gnomAD v2 gnomAD v4 |
14 | g.28767681G>C | CA486098148 | FOXG1 | c.402G>C (p.Pro134=)
| dbSNP |
14 | g.28767681G= | CA2125999331 | FOXG1 | c.402G= (p.Pro134=)
| |
14 | g.28767681G>T | CA486098149 | FOXG1 | c.402G>T (p.Pro134=)
| |
14 | g.28767685del | CA1139663425 | FOXG1 | c.406del (p.Glu136SerfsTer?)
| ClinVar dbSNP gnomAD v4 |
14 | g.28767682G>A | CA389475021 | FOXG1 | c.403G>A (p.Gly135Arg)
| dbSNP gnomAD v4 |
14 | g.28767682G>C | CA389475022 | FOXG1 | c.403G>C (p.Gly135Arg)
| |
14 | g.28767682G= | CA2125999335 | FOXG1 | c.403G= (p.Gly135=)
| |
14 | g.28767682G>T | CA389475023 | FOXG1 | c.403G>T (p.Gly135Trp)
| |
14 | g.28767683G>A | CA389475024 | FOXG1 | c.404G>A (p.Gly135Glu)
| dbSNP |
14 | g.28767683G>C | CA389475025 | FOXG1 | c.404G>C (p.Gly135Ala)
| |
14 | g.28767683G= | CA2125999339 | FOXG1 | c.404G= (p.Gly135=)
| |
14 | g.28767683G>T | CA389475026 | FOXG1 | c.404G>T (p.Gly135Val)
| ClinVar dbSNP gnomAD v3 gnomAD v4 |
14 | g.28767684G>A | CA486098156 | FOXG1 | c.405G>A (p.Gly135=)
| ClinVar dbSNP |
14 | g.28767684G>C | CA486098155 | FOXG1 | c.405G>C (p.Gly135=)
| dbSNP gnomAD v4 |
14 | g.28767684G= | CA2125999342 | FOXG1 | c.405G= (p.Gly135=)
| |
14 | g.28767684G>T | CA486098154 | FOXG1 | c.405G>T (p.Gly135=)
| gnomAD v4 |
14 | g.28767685G>A | CA389475028 | FOXG1 | c.406G>A (p.Glu136Lys)
| gnomAD v4 |
14 | g.28767685G>C | CA389475027 | FOXG1 | c.406G>C (p.Glu136Gln)
| |
14 | g.28767685G= | CA2125999349 | FOXG1 | c.406G= (p.Glu136=)
| |
14 | g.28767685G>T | CA16606550 | FOXG1 | c.406G>T (p.Glu136Ter)
| ClinVar dbSNP |
14 | g.28767688_28767711del | CA2580088000 | FOXG1 | c.409_432del (p.Leu137_Glu144del)
| ClinVar |
14 | g.28767687_28767748del | CA2832528760 | FOXG1 | c.408_469del (p.Leu137GlyfsTer?)
| |
14 | g.28767686A>C | CA389475029 | FOXG1 | c.407A>C (p.Glu136Ala)
| |
14 | g.28767686A>G | CA389475030 | FOXG1 | c.407A>G (p.Glu136Gly)
| |
14 | g.28767686A>T | CA389475031 | FOXG1 | c.407A>T (p.Glu136Val)
| |
14 | g.28767687G>A | CA486098157 | FOXG1 | c.408G>A (p.Glu136=)
| gnomAD v4 |
14 | g.28767687G>C | CA389475032 | FOXG1 | c.408G>C (p.Glu136Asp)
| |
14 | g.28767687G>T | CA389475033 | FOXG1 | c.408G>T (p.Glu136Asp)
| |
14 | g.28767688C>A | CA389475034 | FOXG1 | c.409C>A (p.Leu137Met)
| |
14 | g.28767688C= | CA2125999352 | FOXG1 | c.409C= (p.Leu137=)
| |
14 | g.28767688C>G | CA389475035 | FOXG1 | c.409C>G (p.Leu137Val)
| |
14 | g.28767688C>T | CA486098159 | FOXG1 | c.409C>T (p.Leu137=)
| dbSNP gnomAD v2 gnomAD v4 |
14 | g.28767689T>A | CA389475036 | FOXG1 | c.410T>A (p.Leu137Gln)
| |
14 | g.28767689T>C | CA389475037 | FOXG1 | c.410T>C (p.Leu137Pro)
| |
14 | g.28767689T>G | CA389475038 | FOXG1 | c.410T>G (p.Leu137Arg)
| |
14 | g.28767690G>A | CA7140597 | FOXG1 | c.411G>A (p.Leu137=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.28767690G>C | CA7140596 | FOXG1 | c.411G>C (p.Leu137=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.28767690G= | CA2125999354 | FOXG1 | c.411G= (p.Leu137=)
| |
14 | g.28767690G>T | CA486098160 | FOXG1 | c.411G>T (p.Leu137=)
| |
14 | g.28767691G>A | CA389475041 | FOXG1 | c.412G>A (p.Ala138Thr)
| ClinVar dbSNP gnomAD v3 gnomAD v4 |
14 | g.28767691G>C | CA389475040 | FOXG1 | c.412G>C (p.Ala138Pro)
| dbSNP gnomAD v3 gnomAD v4 |
14 | g.28767691G= | CA2125999358 | FOXG1 | c.412G= (p.Ala138=)
| |
14 | g.28767691G>T | CA389475039 | FOXG1 | c.412G>T (p.Ala138Ser)
| |
14 | g.28767692del | CA2697553884 | FOXG1 | c.413del (p.Ala138GlyfsTer?)
| ClinVar |
14 | g.28767692C>A | CA389475042 | FOXG1 | c.413C>A (p.Ala138Glu)
| |
14 | g.28767692C>G | CA389475043 | FOXG1 | c.413C>G (p.Ala138Gly)
| COSMIC |
14 | g.28767692C>T | CA389475044 | FOXG1 | c.413C>T (p.Ala138Val)
| ClinVar gnomAD v4 |
14 | g.28767693G>A | CA486098162 | FOXG1 | c.414G>A (p.Ala138=)
| |
14 | g.28767693G>C | CA486098163 | FOXG1 | c.414G>C (p.Ala138=)
| gnomAD v4 |
14 | g.28767693G= | CA2125999361 | FOXG1 | c.414G= (p.Ala138=)
| |
14 | g.28767693G>T | CA258396567 | FOXG1 | c.414G>T (p.Ala138=)
| ClinVar dbSNP gnomAD v2 gnomAD v4 |
14 | g.28767694C>A | CA389475045 | FOXG1 | c.415C>A (p.Pro139Thr)
| |
14 | g.28767694C= | CA2125999363 | FOXG1 | c.415C= (p.Pro139=)
| |
14 | g.28767694C>G | CA389475046 | FOXG1 | c.415C>G (p.Pro139Ala)
| |
14 | g.28767694C>T | CA389475047 | FOXG1 | c.415C>T (p.Pro139Ser)
| ClinVar dbSNP gnomAD v2 gnomAD v4 |
14 | g.28767695C>A | CA389475050 | FOXG1 | c.416C>A (p.Pro139His)
| |
14 | g.28767695C= | CA2125999365 | FOXG1 | c.416C= (p.Pro139=)
| |
14 | g.28767695C>G | CA389475049 | FOXG1 | c.416C>G (p.Pro139Arg)
| gnomAD v4 |
14 | g.28767695C>T | CA389475048 | FOXG1 | c.416C>T (p.Pro139Leu)
| dbSNP gnomAD v4 |
14 | g.28767696C>A | CA486098164 | FOXG1 | c.417C>A (p.Pro139=)
| dbSNP gnomAD v4 |
14 | g.28767696C= | CA2125999368 | FOXG1 | c.417C= (p.Pro139=)
| |
14 | g.28767696C>G | CA486098165 | FOXG1 | c.417C>G (p.Pro139=)
| ClinVar |
14 | g.28767696C>T | CA258396568 | FOXG1 | c.417C>T (p.Pro139=)
| ClinVar dbSNP gnomAD v4 |
14 | g.28767697G>A | CA389475051 | FOXG1 | c.418G>A (p.Val140Ile)
| ClinVar dbSNP gnomAD v2 gnomAD v4 |
14 | g.28767697G>C | CA389475052 | FOXG1 | c.418G>C (p.Val140Leu)
| |
14 | g.28767697G= | CA2125999371 | FOXG1 | c.418G= (p.Val140=)
| |
14 | g.28767697G>T | CA389475053 | FOXG1 | c.418G>T (p.Val140Phe)
| |
14 | g.28767698T>A | CA389475054 | FOXG1 | c.419T>A (p.Val140Asp)
| dbSNP |
14 | g.28767698T>C | CA389475055 | FOXG1 | c.419T>C (p.Val140Ala)
| |
14 | g.28767698T>G | CA389475056 | FOXG1 | c.419T>G (p.Val140Gly)
| |
14 | g.28767698T= | CA2125999375 | FOXG1 | c.419T= (p.Val140=)
| |
14 | g.28767699C>A | CA16607633 | FOXG1 | c.420C>A (p.Val140=)
| ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.28767699C= | CA2125999380 | FOXG1 | c.420C= (p.Val140=)
| |
14 | g.28767699C>G | CA486098167 | FOXG1 | c.420C>G (p.Val140=)
| |
14 | g.28767699C>T | CA16606973 | FOXG1 | c.420C>T (p.Val140=)
| ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.28767700G>A | CA389475057 | FOXG1 | c.421G>A (p.Gly141Arg)
| ClinVar dbSNP gnomAD v4 |
14 | g.28767700G>C | CA389475059 | FOXG1 | c.421G>C (p.Gly141Arg)
| dbSNP gnomAD v4 |
14 | g.28767700G= | CA2125999384 | FOXG1 | c.421G= (p.Gly141=)
| |
14 | g.28767700G>T | CA389475058 | FOXG1 | c.421G>T (p.Gly141Trp)
| gnomAD v4 |
14 | g.28767701G>A | CA389475060 | FOXG1 | c.422G>A (p.Gly141Glu)
| |
14 | g.28767701G>C | CA389475061 | FOXG1 | c.422G>C (p.Gly141Ala)
| |
14 | g.28767701G>T | CA389475062 | FOXG1 | c.422G>T (p.Gly141Val)
| ClinVar gnomAD v4 |
14 | g.28767702G>A | CA486098169 | FOXG1 | c.423G>A (p.Gly141=)
| gnomAD v4 |
14 | g.28767702G>C | CA486098171 | FOXG1 | c.423G>C (p.Gly141=)
| |
14 | g.28767702G>T | CA486098170 | FOXG1 | c.423G>T (p.Gly141=)
| ClinVar |
14 | g.28767703C>A | CA389475063 | FOXG1 | c.424C>A (p.Pro142Thr)
| gnomAD v4 |
14 | g.28767703C>G | CA389475064 | FOXG1 | c.424C>G (p.Pro142Ala)
| ClinVar |
14 | g.28767703C>T | CA389475065 | FOXG1 | c.424C>T (p.Pro142Ser)
| ClinVar dbSNP gnomAD v4 |
14 | g.28767704C>A | CA389475066 | FOXG1 | c.425C>A (p.Pro142Gln)
| gnomAD v4 |
14 | g.28767704C>G | CA389475067 | FOXG1 | c.425C>G (p.Pro142Arg)
| gnomAD v4 |
14 | g.28767704C>T | CA389475068 | FOXG1 | c.425C>T (p.Pro142Leu)
| gnomAD v4 |
14 | g.28767705G>A | CA486098172 | FOXG1 | c.426G>A (p.Pro142=)
| dbSNP gnomAD v4 |
14 | g.28767705G>C | CA486098173 | FOXG1 | c.426G>C (p.Pro142=)
| |
14 | g.28767705G= | CA2125999388 | FOXG1 | c.426G= (p.Pro142=)
| |
14 | g.28767705G>T | CA486098175 | FOXG1 | c.426G>T (p.Pro142=)
| ClinVar |
14 | g.28767706G>A | CA389475069 | FOXG1 | c.427G>A (p.Asp143Asn)
| |
14 | g.28767706G>C | CA389475070 | FOXG1 | c.427G>C (p.Asp143His)
| |
14 | g.28767706G>T | CA389475071 | FOXG1 | c.427G>T (p.Asp143Tyr)
| |
14 | g.28767707A>C | CA389475072 | FOXG1 | c.428A>C (p.Asp143Ala)
| |
14 | g.28767707A>G | CA389475074 | FOXG1 | c.428A>G (p.Asp143Gly)
| gnomAD v4 |
14 | g.28767707A>T | CA389475073 | FOXG1 | c.428A>T (p.Asp143Val)
| |
14 | g.28767708C>A | CA389475075 | FOXG1 | c.429C>A (p.Asp143Glu)
| dbSNP gnomAD v2 gnomAD v4 |
14 | g.28767708C= | CA2125999393 | FOXG1 | c.429C= (p.Asp143=)
| |
14 | g.28767708C>G | CA7140598 | FOXG1 | c.429C>G (p.Asp143Glu)
| ClinVar dbSNP ExAC gnomAD v4 |
14 | g.28767708C>T | CA486098178 | FOXG1 | c.429C>T (p.Asp143=)
| dbSNP gnomAD v2 gnomAD v4 |
14 | g.28767709G>A | CA206112 | FOXG1 | c.430G>A (p.Glu144Lys)
| ClinVar dbSNP |
14 | g.28767709G>C | CA389475076 | FOXG1 | c.430G>C (p.Glu144Gln)
| gnomAD v4 |
14 | g.28767709G= | CA2125999403 | FOXG1 | c.430G= (p.Glu144=)
| |
14 | g.28767709G>T | CA389475077 | FOXG1 | c.430G>T (p.Glu144Ter)
| ClinVar dbSNP |
14 | g.28767709_28767712delinsGAGA | CA2125999406 | FOXG1 | c.430_433delinsGAGA (p.Glu144=)
| |
14 | g.28767716_28767721dup | CA915948873 | FOXG1 | c.437_442dup (p.Lys147_Gly148insGluLys)
| ClinVar dbSNP |
14 | g.28767710A>C | CA389475078 | FOXG1 | c.431A>C (p.Glu144Ala)
| |
14 | g.28767710A>G | CA389475079 | FOXG1 | c.431A>G (p.Glu144Gly)
| |
14 | g.28767710A>T | CA389475080 | FOXG1 | c.431A>T (p.Glu144Val)
| gnomAD v4 |
14 | g.28767712_28767714del | CA613324872 | FOXG1 | c.433_435del (p.Lys145del)
| ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.28767711G>A | CA486098182 | FOXG1 | c.432G>A (p.Glu144=)
| gnomAD v4 |
14 | g.28767711G>C | CA314586 | FOXG1 | c.432G>C (p.Glu144Asp)
| ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.28767711G= | CA2125999411 | FOXG1 | c.432G= (p.Glu144=)
| |
14 | g.28767711G>T | CA389475081 | FOXG1 | c.432G>T (p.Glu144Asp)
| |
14 | g.28767712A= | CA2125999416 | FOXG1 | c.433A= (p.Lys145=)
| |
14 | g.28767712A>C | CA389475082 | FOXG1 | c.433A>C (p.Lys145Gln)
| |
14 | g.28767712A>G | CA389475083 | FOXG1 | c.433A>G (p.Lys145Glu)
| dbSNP gnomAD v3 gnomAD v4 |
14 | g.28767712A>T | CA389475084 | FOXG1 | c.433A>T (p.Lys145Ter)
| |
14 | g.28767712_28767715delinsAAGG | CA2125999415 | FOXG1 | c.433_436delinsAAGG (p.Lys145=)
| |
14 | g.28767713A= | CA2125999419 | FOXG1 | c.434A= (p.Lys145=)
| |
14 | g.28767713A>C | CA389475087 | FOXG1 | c.434A>C (p.Lys145Thr)
| dbSNP gnomAD v3 gnomAD v4 |
14 | g.28767713A>G | CA389475085 | FOXG1 | c.434A>G (p.Lys145Arg)
| gnomAD v4 |
14 | g.28767713A>T | CA389475086 | FOXG1 | c.434A>T (p.Lys145Met)
| |
14 | g.28767715_28767717del | CA7140599 | FOXG1 | c.436_438del (p.Glu146del)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.28767714G>A | CA486098183 | FOXG1 | c.435G>A (p.Lys145=)
| dbSNP gnomAD v2 gnomAD v4 |
14 | g.28767714G>C | CA389475088 | FOXG1 | c.435G>C (p.Lys145Asn)
| |
14 | g.28767714G= | CA2125999421 | FOXG1 | c.435G= (p.Lys145=)
| |
14 | g.28767714G>T | CA389475089 | FOXG1 | c.435G>T (p.Lys145Asn)
| COSMIC |
14 | g.28767714_28767715del | CA2739291836 | FOXG1 | c.435_436del (p.Lys147GlyfsTer?)
| |
14 | g.28767715G>A | CA389475090 | FOXG1 | c.436G>A (p.Glu146Lys)
| |
14 | g.28767715G>C | CA389475091 | FOXG1 | c.436G>C (p.Glu146Gln)
| dbSNP gnomAD v4 |
14 | g.28767715G= | CA2125999424 | FOXG1 | c.436G= (p.Glu146=)
| |
14 | g.28767715G>T | CA389475092 | FOXG1 | c.436G>T (p.Glu146Ter)
| ClinVar dbSNP |
14 | g.28767716A= | CA2125999432 | FOXG1 | c.437A= (p.Glu146=)
| |
14 | g.28767716A>C | CA389475093 | FOXG1 | c.437A>C (p.Glu146Ala)
| gnomAD v4 |
14 | g.28767716A>G | CA16607634 | FOXG1 | c.437A>G (p.Glu146Gly)
| ClinVar dbSNP |
14 | g.28767716A>T | CA258396569 | FOXG1 | c.437A>T (p.Glu146Val)
| dbSNP |
14 | g.28767717G>A | CA258396570 | FOXG1 | c.438G>A (p.Glu146=)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.28767717G>C | CA389475094 | FOXG1 | c.438G>C (p.Glu146Asp)
| gnomAD v4 |
14 | g.28767717G= | CA2125999436 | FOXG1 | c.438G= (p.Glu146=)
| |
14 | g.28767717G>T | CA389475095 | FOXG1 | c.438G>T (p.Glu146Asp)
| |
14 | g.28767718A>C | CA389475096 | FOXG1 | c.439A>C (p.Lys147Gln)
| |
14 | g.28767718A>G | CA389475098 | FOXG1 | c.439A>G (p.Lys147Glu)
| |
14 | g.28767718A>T | CA389475097 | FOXG1 | c.439A>T (p.Lys147Ter)
| ClinVar |
14 | g.28767719A= | CA2125999440 | FOXG1 | c.440A= (p.Lys147=)
| |
14 | g.28767719A>C | CA389475099 | FOXG1 | c.440A>C (p.Lys147Thr)
| |
14 | g.28767719A>G | CA389475101 | FOXG1 | c.440A>G (p.Lys147Arg)
| ClinVar dbSNP |
14 | g.28767719A>T | CA389475100 | FOXG1 | c.440A>T (p.Lys147Met)
| ClinVar dbSNP |
14 | g.28767720G>A | CA486098186 | FOXG1 | c.441G>A (p.Lys147=)
| ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.28767720G>C | CA389475102 | FOXG1 | c.441G>C (p.Lys147Asn)
| |
14 | g.28767720G= | CA2125999442 | FOXG1 | c.441G= (p.Lys147=)
| |
14 | g.28767720G>T | CA389475103 | FOXG1 | c.441G>T (p.Lys147Asn)
| gnomAD v4 |
14 | g.28767721G>A | CA389475104 | FOXG1 | c.442G>A (p.Gly148Ser)
| |
14 | g.28767721G>C | CA389475105 | FOXG1 | c.442G>C (p.Gly148Arg)
| |
14 | g.28767721G= | CA2125999446 | FOXG1 | c.442G= (p.Gly148=)
| |
14 | g.28767721G>T | CA389475106 | FOXG1 | c.442G>T (p.Gly148Cys)
| dbSNP gnomAD v2 |
14 | g.28767729_28767734dup | CA7140600 | FOXG1 | c.450_455dup (p.Gly152_Gly153insAlaGly)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
14 | g.28767722G>A | CA389475107 | FOXG1 | c.443G>A (p.Gly148Asp)
| ClinVar dbSNP gnomAD v2 gnomAD v4 |
14 | g.28767722G>C | CA389475108 | FOXG1 | c.443G>C (p.Gly148Ala)
| ClinVar |
14 | g.28767722G= | CA2125999448 | FOXG1 | c.443G= (p.Gly148=)
| |
14 | g.28767722G>T | CA7140601 | FOXG1 | c.443G>T (p.Gly148Val)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |