List of variants reported as likely pathogenic for Intellectual disability, X-linked, syndromic 33 by Genome Medicine, Institute for Basic Research in Developmental Disabilities

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Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_004606.5(TAF1):c.1520A>G (p.Asp507Gly)	rs1602481623
NM_004606.5(TAF1):c.1726C>T (p.Pro576Ser)	rs864321630
NM_004606.5(TAF1):c.1979G>A (p.Gly660Asp)	rs1602489684
NM_004606.5(TAF1):c.2359T>C (p.Cys787Arg)	rs864321628
NM_004606.5(TAF1):c.2608C>T (p.Arg870Cys)	rs1602506017
NM_004606.5(TAF1):c.2894C>T (p.Ser965Phe)	rs1057518019
NM_004606.5(TAF1):c.2975C>T (p.Thr992Ile)	rs1602520317
NM_004606.5(TAF1):c.3508C>T (p.Arg1170Cys)	rs1569301036
NM_004606.5(TAF1):c.3648A>G (p.Gln1216=)	rs2034990430
NM_004606.5(TAF1):c.3700C>T (p.Arg1234Trp)	rs1602538353
NM_004606.5(TAF1):c.3973G>A (p.Val1325Ile)	rs1131691982
NM_004606.5(TAF1):c.4382A>T (p.Asn1461Ile)	rs1602572645
NM_004606.5(TAF1):c.4394A>G (p.His1465Arg)	rs1064793874
NM_004606.5(TAF1):c.4520C>T (p.Ala1507Val)	rs1602624950

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