ClinVar Miner

List of variants in gene FOXG1 reported as likely benign for X-linked syndromic intellectual disability

Included ClinVar conditions (212):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 43
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HGVS dbSNP
NM_005249.5(FOXG1):c.1122C>T (p.Tyr374=) rs777855975
NM_005249.5(FOXG1):c.1161G>A (p.Ser387=) rs147154860
NM_005249.5(FOXG1):c.1200C>T (p.Tyr400=) rs138747073
NM_005249.5(FOXG1):c.1320C>G (p.Ser440=) rs1057524328
NM_005249.5(FOXG1):c.1323C>T (p.Ser441=) rs144434028
NM_005249.5(FOXG1):c.1399C>T (p.Leu467=) rs371279404
NM_005249.5(FOXG1):c.141_143CCA[8] (p.His57dup) rs587783630
NM_005249.5(FOXG1):c.159C>T (p.His53=) rs769410384
NM_005249.5(FOXG1):c.164_166ACC[4] (p.His57dup) rs772407998
NM_005249.5(FOXG1):c.183_206del (p.Ala62_Pro69del) rs587783632
NM_005249.5(FOXG1):c.189G>T (p.Pro63=) rs796052451
NM_005249.5(FOXG1):c.196C>G (p.Pro66Ala)
NM_005249.5(FOXG1):c.201G>T (p.Pro67=) rs587780944
NM_005249.5(FOXG1):c.209_211AGC[5] (p.Gln73dup) rs398124201
NM_005249.5(FOXG1):c.209_229del (p.Gln70_Pro76del) rs1466028633
NM_005249.5(FOXG1):c.209_232del (p.Gln70_Pro77del) rs794726920
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.219_221GCC[5] (p.Pro80del) rs786200975
NM_005249.5(FOXG1):c.219_221GCC[7] (p.Pro80dup) rs786200975
NM_005249.5(FOXG1):c.233_247del (p.Pro78_Pro82del) rs1466765630
NM_005249.5(FOXG1):c.245C>A (p.Pro82Gln) rs796052453
NM_005249.5(FOXG1):c.246G>C (p.Pro82=) rs1555321242
NM_005249.5(FOXG1):c.281A>C (p.Asp94Ala) rs1206977063
NM_005249.5(FOXG1):c.287A>G (p.Asp96Gly)
NM_005249.5(FOXG1):c.323C>T (p.Pro108Leu) rs1594383213
NM_005249.5(FOXG1):c.324A>G (p.Pro108=) rs750512461
NM_005249.5(FOXG1):c.347T>C (p.Leu116Pro) rs1594383240
NM_005249.5(FOXG1):c.417C>T (p.Pro139=) rs1018810212
NM_005249.5(FOXG1):c.420C>A (p.Val140=) rs967306759
NM_005249.5(FOXG1):c.431_436AGAAGG[3] (p.144_145EK[3]) rs1594383335
NM_005249.5(FOXG1):c.432G>C (p.Glu144Asp) rs547825816
NM_005249.5(FOXG1):c.447C>T (p.Ala149=) rs112803404
NM_005249.5(FOXG1):c.456G>T (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.503G>C (p.Gly168Ala) rs148157138
NM_005249.5(FOXG1):c.555C>T (p.Ser185=) rs778154529
NM_005249.5(FOXG1):c.594C>G (p.Pro198=) rs141088742
NM_005249.5(FOXG1):c.618C>T (p.Gly206=) rs930327703
NM_005249.5(FOXG1):c.798C>T (p.Ile266=) rs753051078
NM_005249.5(FOXG1):c.852G>A (p.Leu284=) rs537686463
NM_005249.5(FOXG1):c.887G>T (p.Gly296Val)

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