ClinVar Miner

List of variants in gene FOXG1 reported as pathogenic for not provided

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Gene type:
ClinVar version:
Total variants: 81
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HGVS dbSNP gnomAD frequency
NM_005249.5(FOXG1):c.239dup (p.Ala81fs) rs796052474 0.00001
GRCh37/hg19 14q12(chr14:28428064-29988744)x1
GRCh37/hg19 14q12(chr14:28484920-29691434)x1
GRCh37/hg19 14q12(chr14:28836918-29955663)x1
NM_005249.4(FOXG1):c.[563C>G(;)644_645delTCinsCT]
NM_005249.5(FOXG1):c.1014dup (p.Met339fs) rs1881816066
NM_005249.5(FOXG1):c.1058dup (p.Asn353fs) rs1555321400
NM_005249.5(FOXG1):c.1111G>T (p.Glu371Ter) rs2138661969
NM_005249.5(FOXG1):c.1160_1161delinsGTC (p.Ser387fs) rs1057518196
NM_005249.5(FOXG1):c.1168dup (p.Cys390fs) rs1881820386
NM_005249.5(FOXG1):c.1170C>A (p.Cys390Ter) rs1392520466
NM_005249.5(FOXG1):c.1178C>G (p.Ser393Trp) rs1085307753
NM_005249.5(FOXG1):c.1200C>A (p.Tyr400Ter) rs138747073
NM_005249.5(FOXG1):c.1200C>G (p.Tyr400Ter) rs138747073
NM_005249.5(FOXG1):c.1248C>G (p.Tyr416Ter) rs786204999
NM_005249.5(FOXG1):c.1344dup (p.Ser449fs) rs2138662268
NM_005249.5(FOXG1):c.1366_1375del (p.Arg457fs)
NM_005249.5(FOXG1):c.136C>T (p.Gln46Ter) rs786205000
NM_005249.5(FOXG1):c.136dup (p.Gln46fs) rs587783629
NM_005249.5(FOXG1):c.1402_1405del (p.Ser468fs) rs796052486
NM_005249.5(FOXG1):c.177_186dup (p.Pro63fs) rs1555321206
NM_005249.5(FOXG1):c.178_280del (p.Pro60fs) rs1594382930
NM_005249.5(FOXG1):c.214C>T (p.Gln72Ter) rs1555321237
NM_005249.5(FOXG1):c.217C>T (p.Gln73Ter) rs796052458
NM_005249.5(FOXG1):c.221_228delinsAGCCGCCCCC (p.Pro74fs) rs1594383056
NM_005249.5(FOXG1):c.225_226delinsACCG (p.Pro77fs) rs796052485
NM_005249.5(FOXG1):c.256C>T (p.Gln86Ter) rs398124202
NM_005249.5(FOXG1):c.256del (p.Gln86fs) rs786205001
NM_005249.5(FOXG1):c.256dup (p.Gln86fs) rs786205001
NM_005249.5(FOXG1):c.298del (p.Gln100fs) rs587783636
NM_005249.5(FOXG1):c.301C>T (p.Gln101Ter) rs1881788747
NM_005249.5(FOXG1):c.383dup (p.Glu129fs) rs796052476
NM_005249.5(FOXG1):c.385G>T (p.Glu129Ter) rs1555321264
NM_005249.5(FOXG1):c.399del (p.Pro134fs) rs796052477
NM_005249.5(FOXG1):c.406G>T (p.Glu136Ter) rs1057520663
NM_005249.5(FOXG1):c.436G>T (p.Glu146Ter) rs1555321279
NM_005249.5(FOXG1):c.460G>T (p.Glu154Ter) rs1057520780
NM_005249.5(FOXG1):c.460del (p.Glu154fs) rs398124204
NM_005249.5(FOXG1):c.460dup (p.Glu154fs) rs398124204
NM_005249.5(FOXG1):c.499del (p.Glu167fs)
NM_005249.5(FOXG1):c.506del (p.Gly169fs) rs1452295073
NM_005249.5(FOXG1):c.506dup (p.Lys170fs) rs1452295073
NM_005249.5(FOXG1):c.511G>T (p.Glu171Ter) rs1057517859
NM_005249.5(FOXG1):c.526_529dup (p.Gly177fs) rs1594383538
NM_005249.5(FOXG1):c.538G>T (p.Glu180Ter) rs1555321302
NM_005249.5(FOXG1):c.543G>T (p.Lys181Asn) rs767961672
NM_005249.5(FOXG1):c.552del (p.Phe184fs) rs1594383576
NM_005249.5(FOXG1):c.559A>T (p.Asn187Tyr) rs2138661139
NM_005249.5(FOXG1):c.561C>A (p.Asn187Lys) rs796052462
NM_005249.5(FOXG1):c.561C>G (p.Asn187Lys) rs796052462
NM_005249.5(FOXG1):c.565C>T (p.Leu189Phe) rs1555321308
NM_005249.5(FOXG1):c.585_586delinsTT (p.Gln196Ter) rs1064797030
NM_005249.5(FOXG1):c.586C>T (p.Gln196Ter) rs796052463
NM_005249.5(FOXG1):c.590G>T (p.Ser197Ile) rs1881802605
NM_005249.5(FOXG1):c.610C>T (p.Leu204Phe) rs786205006
NM_005249.5(FOXG1):c.622T>C (p.Tyr208His)
NM_005249.5(FOXG1):c.624C>G (p.Tyr208Ter) rs267606826
NM_005249.5(FOXG1):c.645C>G (p.Phe215Leu) rs1057518165
NM_005249.5(FOXG1):c.648_655del (p.Tyr217fs) rs727503934
NM_005249.5(FOXG1):c.651C>G (p.Tyr217Ter) rs796052464
NM_005249.5(FOXG1):c.653A>G (p.Tyr218Cys) rs1881804364
NM_005249.5(FOXG1):c.667C>T (p.Gln223Ter) rs796052465
NM_005249.5(FOXG1):c.676C>T (p.Gln226Ter) rs1131691540
NM_005249.5(FOXG1):c.695A>C (p.Asn232Thr)
NM_005249.5(FOXG1):c.695A>G (p.Asn232Ser) rs2138661390
NM_005249.5(FOXG1):c.703del (p.Leu235fs) rs1064793481
NM_005249.5(FOXG1):c.706A>G (p.Asn236Asp)
NM_005249.5(FOXG1):c.708C>A (p.Asn236Lys) rs796052468
NM_005249.5(FOXG1):c.748G>A (p.Gly250Ser)
NM_005249.5(FOXG1):c.748G>C (p.Gly250Arg) rs2138661461
NM_005249.5(FOXG1):c.755G>T (p.Gly252Val) rs587783640
NM_005249.5(FOXG1):c.758_761dup (p.Tyr254Ter) rs1594383773
NM_005249.5(FOXG1):c.763T>C (p.Trp255Arg)
NM_005249.5(FOXG1):c.770T>C (p.Leu257Pro) rs1555321353
NM_005249.5(FOXG1):c.797T>A (p.Ile266Asn) rs886041744
NM_005249.5(FOXG1):c.799G>A (p.Gly267Ser) rs587783643
NM_005249.5(FOXG1):c.855del (p.Phe286fs) rs1555321366
NM_005249.5(FOXG1):c.85C>T (p.Gln29Ter)
NM_005249.5(FOXG1):c.920dup (p.Tyr307Ter) rs1881812495
NM_005249.5(FOXG1):c.923G>A (p.Trp308Ter) rs2138661744
NM_005249.5(FOXG1):c.958del (p.Arg320fs) rs1555321382

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