"Fulgent Genetics, Fulgent Genetics"[submitter] AND "TAF1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 697120	NM_004606.5(TAF1):c.422C>T (p.Pro141Leu)	TAF1 (P141L)	Single nucleotide variant (missense variant +1 more)	X-linked dystonia-parkinsonism +2 more	GBenign/Likely benign
Select item 700214	NM_004606.5(TAF1):c.4155G>A (p.Thr1385=)	TAF1	Single nucleotide variant (synonymous variant +1 more)	X-linked dystonia-parkinsonism +2 more	GBenign/Likely benign
Select item 698491	NM_004606.5(TAF1):c.4521G>A (p.Ala1507=)	TAF1	Single nucleotide variant (synonymous variant +1 more)	X-linked dystonia-parkinsonism +2 more	GBenign/Likely benign
Select item 695775	NM_004606.5(TAF1):c.4698G>A (p.Arg1566=)	TAF1	Single nucleotide variant (synonymous variant +1 more)	Intellectual disability, X-linked, syndromic 33 +2 more	GBenign/Likely benign
Select item 696096	NM_004606.5(TAF1):c.4708C>T (p.Leu1570=)	TAF1	Single nucleotide variant (synonymous variant +1 more)	X-linked dystonia-parkinsonism +2 more	GBenign
Select item 695493	NM_004606.5(TAF1):c.4754-4A>G	TAF1	Single nucleotide variant (intron variant)	Intellectual disability, X-linked, syndromic 33 +2 more	GLikely benign

ClinVar