"Ambry Genetics"[submitter] AND "CD8B"[gene] - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3140706	NM_172213.5(CD8B):c.659A>G (p.Gln220Arg)	CD8B (Q190R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2468775	NM_004931.5(CD8B):c.607C>T (p.Arg203Cys)	CD8B (R173C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2339712	NM_004931.5(CD8B):c.568G>A (p.Ala190Thr)	CD8B (A190T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2340963	NM_004931.5(CD8B):c.508C>G (p.Pro170Ala)	CD8B (P170A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3140705	NM_004931.5(CD8B):c.482A>G (p.Glu161Gly)	CD8B (E161G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2251046	NM_004931.5(CD8B):c.380G>T (p.Gly127Val)	CD8B (G127V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140704	NM_004931.5(CD8B):c.379G>A (p.Gly127Arg)	CD8B (G127R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2224435	NM_004931.5(CD8B):c.358G>A (p.Gly120Arg)	CD8B (G120R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140703	NM_004931.5(CD8B):c.355G>A (p.Val119Ile)	CD8B (V119I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2300020	NM_004931.5(CD8B):c.350T>C (p.Met117Thr)	CD8B (M117T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140702	NM_004931.5(CD8B):c.331A>C (p.Ser111Arg)	CD8B (S111R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525621	NM_004931.5(CD8B):c.293G>A (p.Arg98Gln)	CD8B (R98Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2591344	NM_004931.5(CD8B):c.178G>A (p.Ala60Thr)	CD8B (A60T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2249433	NM_004931.5(CD8B):c.134T>C (p.Ile45Thr)	CD8B (I45T)	Single nucleotide variant (missense variant)	not specified	GLikely benign