"Ambry Genetics"[submitter] AND "CD4"[gene] - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2459148	NM_000616.5(CD4):c.369C>A (p.Phe123Leu)	CD4 (F123L +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2476258	NM_000616.5(CD4):c.557T>C (p.Val186Ala)	CD4 (V131A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3140589	NM_000616.5(CD4):c.676G>A (p.Ala226Thr)	CD4 (A171T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2293145	NM_000616.5(CD4):c.982T>C (p.Cys328Arg)	CD4 (C273R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2360144	NM_000616.5(CD4):c.1055C>G (p.Ser352Trp)	CD4 (S297W +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2605865	NM_000616.5(CD4):c.1082T>C (p.Leu361Pro)	CD4 (L361P +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2529787	NM_000616.5(CD4):c.1183C>A (p.Gln395Lys)	CD4 (Q122K +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2278141	NM_000616.5(CD4):c.1219G>A (p.Gly407Ser)	CD4 (G228S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2377032	NM_000616.5(CD4):c.1330A>G (p.Thr444Ala)	CD4 (T171A +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140586	NM_000616.5(CD4):c.1347C>T (p.His449=)	CD4	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3140587	NM_000616.5(CD4):c.1348C>T (p.Arg450Trp)	CD4 (R395W +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance