ClinVar Miner

List of variants in gene FOXG1 reported as likely benign by GeneDx

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 96
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HGVS dbSNP gnomAD frequency
NM_005249.5(FOXG1):c.221C>A (p.Pro74Gln) rs796052452 0.01958
NM_005249.5(FOXG1):c.-269G>C rs973292843 0.00422
NM_005249.5(FOXG1):c.206C>A (p.Pro69Gln) rs727503933 0.00057
NM_005249.5(FOXG1):c.245C>A (p.Pro82Gln) rs796052453 0.00030
NM_005249.5(FOXG1):c.209A>C (p.Gln70Pro) rs587783633 0.00026
NM_005249.5(FOXG1):c.420C>A (p.Val140=) rs967306759 0.00023
NM_005249.5(FOXG1):c.181C>T (p.Pro61Ser) rs762634382 0.00021
NM_005249.5(FOXG1):c.304C>T (p.Leu102=) rs1343209225 0.00020
NM_005249.5(FOXG1):c.1200C>T (p.Tyr400=) rs138747073 0.00019
NM_005249.5(FOXG1):c.852G>A (p.Leu284=) rs537686463 0.00016
NM_005249.5(FOXG1):c.218A>C (p.Gln73Pro) rs760663911 0.00015
NM_005249.5(FOXG1):c.376G>A (p.Gly126Ser) rs796052455 0.00006
NM_005249.5(FOXG1):c.432G>C (p.Glu144Asp) rs547825816 0.00006
NM_005249.5(FOXG1):c.1254C>T (p.Phe418=) rs777770149 0.00005
NM_005249.5(FOXG1):c.1045T>G (p.Ser349Ala) rs796052472 0.00004
NM_005249.5(FOXG1):c.1273T>C (p.Ser425Pro) rs780242359 0.00004
NM_005249.5(FOXG1):c.1313C>T (p.Ala438Val) rs376242569 0.00004
NM_005249.5(FOXG1):c.188C>G (p.Pro63Arg) rs796052478 0.00004
NM_005249.5(FOXG1):c.251C>A (p.Pro84His) rs866815665 0.00004
NM_005249.5(FOXG1):c.455G>C (p.Gly152Ala) rs796052460 0.00004
NM_005249.5(FOXG1):c.1104C>A (p.Val368=) rs780806885 0.00003
NM_005249.5(FOXG1):c.1278G>A (p.Met426Ile) rs747138265 0.00003
NM_005249.5(FOXG1):c.335C>T (p.Pro112Leu) rs1285352804 0.00003
NM_005249.5(FOXG1):c.1341C>T (p.Ala447=) rs200639648 0.00002
NM_005249.5(FOXG1):c.221C>T (p.Pro74Leu) rs796052452 0.00002
NM_005249.5(FOXG1):c.326C>T (p.Pro109Leu) rs398124203 0.00002
NM_005249.5(FOXG1):c.*2A>T rs771359224 0.00001
NM_005249.5(FOXG1):c.105G>A (p.Ala35=) rs753859771 0.00001
NM_005249.5(FOXG1):c.1243A>G (p.Ser415Gly) rs1485738472 0.00001
NM_005249.5(FOXG1):c.1263C>G (p.Val421=) rs373079213 0.00001
NM_005249.5(FOXG1):c.1392G>C (p.Thr464=) rs755772051 0.00001
NM_005249.5(FOXG1):c.150C>T (p.His50=) rs532508999 0.00001
NM_005249.5(FOXG1):c.159C>T (p.His53=) rs769410384 0.00001
NM_005249.5(FOXG1):c.171C>A (p.His57Gln) rs1057522121 0.00001
NM_005249.5(FOXG1):c.240G>A (p.Pro80=) rs1057521165 0.00001
NM_005249.5(FOXG1):c.263G>A (p.Arg88Gln) rs1046668279 0.00001
NM_005249.5(FOXG1):c.318G>A (p.Pro106=) rs1035987967 0.00001
NM_005249.5(FOXG1):c.367G>C (p.Gly123Arg) rs758610493 0.00001
NM_005249.5(FOXG1):c.382G>T (p.Gly128Cys) rs1029176730 0.00001
NM_005249.5(FOXG1):c.504G>A (p.Gly168=) rs1057520499 0.00001
NM_005249.5(FOXG1):c.57C>T (p.Ser19=) rs372915038 0.00001
NM_005249.5(FOXG1):c.984C>T (p.Asn328=) rs774246700 0.00001
NM_005249.5(FOXG1):c.-18C>T rs1057523422
NM_005249.5(FOXG1):c.-210del rs542787885
NM_005249.5(FOXG1):c.-210dup rs542787885
NM_005249.5(FOXG1):c.-26C>G rs1057522652
NM_005249.5(FOXG1):c.-329dup rs1555321095
NM_005249.5(FOXG1):c.115CAC[1] (p.His40del) rs756685121
NM_005249.5(FOXG1):c.1186T>A (p.Cys396Ser) rs1594384203
NM_005249.5(FOXG1):c.1203C>T (p.Ser401=) rs201024952
NM_005249.5(FOXG1):c.1224C>T (p.Asn408=) rs1555321425
NM_005249.5(FOXG1):c.1227G>T (p.Leu409=) rs1311321396
NM_005249.5(FOXG1):c.1320C>G (p.Ser440=) rs1057524328
NM_005249.5(FOXG1):c.132C>A (p.His44Gln) rs796052446
NM_005249.5(FOXG1):c.1395G>A (p.Thr465=) rs369183477
NM_005249.5(FOXG1):c.141CCA[4] (p.His55_His57del) rs587783630
NM_005249.5(FOXG1):c.141CCA[8] (p.His57dup) rs587783630
NM_005249.5(FOXG1):c.182_208del (p.Pro61_Pro69del) rs796052450
NM_005249.5(FOXG1):c.183_206del (p.Ala62_Pro69del) rs587783632
NM_005249.5(FOXG1):c.206C>T (p.Pro69Leu) rs727503933
NM_005249.5(FOXG1):c.206_214dup (p.Pro69_Gln71dup) rs1555321230
NM_005249.5(FOXG1):c.207_236del (p.Gln70_Pro79del) rs1064794158
NM_005249.5(FOXG1):c.209AGC[5] (p.Gln73dup) rs398124201
NM_005249.5(FOXG1):c.209_229del (p.Gln70_Pro76del) rs1466028633
NM_005249.5(FOXG1):c.209_235del (p.Gln70_Pro78del) rs587783634
NM_005249.5(FOXG1):c.209_235dup (p.Gln70_Pro78dup) rs587783634
NM_005249.5(FOXG1):c.213G>A (p.Gln71=) rs1057520541
NM_005249.5(FOXG1):c.227C>T (p.Pro76Leu) rs1381438340
NM_005249.5(FOXG1):c.233_247del (p.Pro78_Pro82del) rs1466765630
NM_005249.5(FOXG1):c.234_235insGCC (p.Pro78_Pro79insAla) rs2138660426
NM_005249.5(FOXG1):c.240G>C (p.Pro80=) rs1057521165
NM_005249.5(FOXG1):c.256C>G (p.Gln86Glu) rs398124202
NM_005249.5(FOXG1):c.268G>T (p.Ala90Ser) rs906816341
NM_005249.5(FOXG1):c.300G>A (p.Gln100=) rs2138660579
NM_005249.5(FOXG1):c.305T>C (p.Leu102Pro) rs1881789009
NM_005249.5(FOXG1):c.329C>G (p.Pro110Arg) rs2138660646
NM_005249.5(FOXG1):c.344C>T (p.Ala115Val) rs796052454
NM_005249.5(FOXG1):c.386_397dup (p.Glu129_Gly132dup) rs796052456
NM_005249.5(FOXG1):c.401C>G (p.Pro134Arg) rs2138660771
NM_005249.5(FOXG1):c.420C>T (p.Val140=) rs967306759
NM_005249.5(FOXG1):c.437A>G (p.Glu146Gly) rs923912596
NM_005249.5(FOXG1):c.447C>G (p.Ala149=) rs112803404
NM_005249.5(FOXG1):c.456G>C (p.Gly152=) rs587783637
NM_005249.5(FOXG1):c.459G>T (p.Gly153=) rs1057520968
NM_005249.5(FOXG1):c.477G>A (p.Ala159=) rs1057523583
NM_005249.5(FOXG1):c.506G>T (p.Gly169Val) rs796052480
NM_005249.5(FOXG1):c.639G>A (p.Lys213=) rs1555321320
NM_005249.5(FOXG1):c.759C>T (p.Asn253=) rs767873754
NM_005249.5(FOXG1):c.801C>A (p.Gly267=) rs1283306011
NM_005249.5(FOXG1):c.907G>A (p.Ala303Thr) rs779697567
NM_005249.5(FOXG1):c.915C>T (p.Ser305=) rs746727507
NM_005249.5(FOXG1):c.91G>A (p.Asp31Asn) rs2138659978
NM_005249.5(FOXG1):c.933G>T (p.Ser311=) rs1481653005
NM_005249.5(FOXG1):c.936C>T (p.Pro312=) rs1555321376
NM_005249.5(FOXG1):c.977G>A (p.Ser326Asn) rs748001255
NM_005249.5(FOXG1):c.9C>T (p.Asp3=) rs764914165

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