List of variants in gene DOCK8 reported as uncertain significance by Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago

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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: 8

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HGVS	dbSNP	gnomAD frequency
NM_203447.4(DOCK8):c.4019A>G (p.Tyr1340Cys)	rs116920018	0.00276
NM_203447.4(DOCK8):c.380G>A (p.Arg127His)	rs150742426	0.00196
NM_203447.4(DOCK8):c.494C>T (p.Ser165Leu)	rs146490788	0.00061
NM_203447.4(DOCK8):c.3216C>G (p.Ile1072Met)	rs370250940	0.00020
NM_203447.4(DOCK8):c.2594T>C (p.Val865Ala)	rs373018701	0.00010
NM_203447.4(DOCK8):c.1609C>T (p.Arg537Trp)	rs544513633	0.00001
NM_203447.4(DOCK8):c.4703A>C (p.Glu1568Ala)	rs2056742806
NM_203447.4(DOCK8):c.5481T>C (p.His1827=)	rs1554708887

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