"PreventionGenetics, part of Exact Sciences"[submitter] AND "CD6"[gene - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3037569	NM_006725.5(CD6):c.49+8C>T	CD6	Single nucleotide variant (intron variant)	CD6-related disorder	GBenign
Select item 3059657	NM_006725.5(CD6):c.567T>C (p.Thr189=)	CD6	Single nucleotide variant (synonymous variant +1 more)	CD6-related disorder	GBenign
Select item 3056065	NM_006725.5(CD6):c.650C>T (p.Thr217Met)	CD6 (T217M)	Single nucleotide variant (missense variant +1 more)	CD6-related disorder	GBenign
Select item 3060458	NM_006725.5(CD6):c.673C>T (p.Arg225Trp)	CD6 (R225W)	Single nucleotide variant (missense variant +1 more)	CD6-related disorder	GBenign
Select item 3059536	NM_006725.5(CD6):c.770C>T (p.Ala257Val)	CD6 (A257V)	Single nucleotide variant (missense variant +1 more)	CD6-related disorder	GBenign
Select item 3059695	NM_006725.5(CD6):c.771G>C (p.Ala257=)	CD6	Single nucleotide variant (synonymous variant +1 more)	CD6-related disorder	GBenign
Select item 3060441	NM_006725.5(CD6):c.811G>A (p.Ala271Thr)	CD6 (A271T)	Single nucleotide variant (missense variant +1 more)	CD6-related disorder	GBenign
Select item 3057359	NM_006725.5(CD6):c.1299C>T (p.Pro433=)	CD6	Single nucleotide variant (synonymous variant +2 more)	CD6-related disorder	GLikely benign
Select item 3042003	NM_006725.5(CD6):c.1362G>A (p.Pro454=)	CD6	Single nucleotide variant (synonymous variant +2 more)	CD6-related disorder	GLikely benign
Select item 3059454	NM_006725.5(CD6):c.1704A>G (p.Ser568=)	CD6	Single nucleotide variant (synonymous variant +1 more)	CD6-related disorder	GBenign
Select item 3059147	NM_006725.5(CD6):c.1815C>T (p.Ala605=)	CD6	Single nucleotide variant (synonymous variant +1 more)	CD6-related disorder	GBenign
Select item 3055886	NM_006725.5(CD6):c.1816G>A (p.Gly606Ser)	CD6 (G565S +2 more)	Single nucleotide variant (missense variant +1 more)	CD6-related disorder	GBenign
Select item 3038452	NM_006725.5(CD6):c.1834T>C (p.Ser612Pro)	CD6 (S571P +2 more)	Single nucleotide variant (missense variant +1 more)	CD6-related disorder	GLikely benign
Select item 3038860	NM_006725.5(CD6):c.1875C>G (p.Ser625=)	CD6	Single nucleotide variant (synonymous variant +1 more)	CD6-related disorder	GBenign
Select item 3039701	NM_006725.5(CD6):c.1971C>T (p.Thr657=)	CD6	Single nucleotide variant (synonymous variant +1 more)	CD6-related disorder	GLikely benign