List of variants in gene TAF1 reported as likely pathogenic for not provided

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_004606.5(TAF1):c.428C>T (p.Pro143Leu)	rs767354861	0.00001
NM_004606.5(TAF1):c.1726C>T (p.Pro576Ser)	rs864321630
NM_004606.5(TAF1):c.2711A>G (p.Tyr904Cys)	rs2148347582
NM_004606.5(TAF1):c.2873C>T (p.Thr958Met)	rs2034628748
NM_004606.5(TAF1):c.2894C>T (p.Ser965Phe)	rs1057518019
NM_004606.5(TAF1):c.3184C>T (p.Arg1062Cys)	rs2034677583
NM_004606.5(TAF1):c.3648A>G (p.Gln1216=)	rs2034990430
NM_004606.5(TAF1):c.3676C>T (p.Arg1226Trp)	rs864321629
NM_004606.5(TAF1):c.3701G>A (p.Arg1234Gln)
NM_004606.5(TAF1):c.3973G>A (p.Val1325Ile)	rs1131691982
NM_004606.5(TAF1):c.4270C>T (p.Arg1424Trp)
NM_004606.5(TAF1):c.4316T>C (p.Leu1439Pro)	rs1555980614
NM_004606.5(TAF1):c.4394A>G (p.His1465Arg)	rs1064793874

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