"Ambry Genetics"[submitter] AND "CD164"[gene] - ClinVar - NCBI

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Items: 8

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2623188	NM_006016.6(CD164):c.571G>A (p.Glu191Lys)	CD164 (E191K +3 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2226743	NM_006016.6(CD164):c.557T>A (p.Phe186Tyr)	CD164 (F167Y +3 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2218974	NM_006016.6(CD164):c.400A>G (p.Thr134Ala)	CD164 (T121A +2 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2550988	NM_006016.6(CD164):c.397T>C (p.Ser133Pro)	CD164 (S133P +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2226373	NM_006016.6(CD164):c.275C>T (p.Ser92Leu)	CD164 (S58L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2275701	NM_006016.6(CD164):c.263A>G (p.Glu88Gly)	CD164 (E88G +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2364879	NM_006016.6(CD164):c.233C>T (p.Thr78Ile)	CD164 (T78I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1968420	NM_006016.6(CD164):c.112C>G (p.Pro38Ala)	CD164 (P38A)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance