"Ambry Genetics"[submitter] AND "NCK1"[gene] - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3298765	NM_001291999.2(NCK1):c.98A>G (p.Asp33Gly)	NCK1 (D33G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3182226	NM_001291999.2(NCK1):c.179A>G (p.Asn60Ser)	NCK1 (N60S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2328857	NM_001291999.2(NCK1):c.188G>A (p.Arg63Gln)	NCK1 (R63Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2466435	NM_001291999.2(NCK1):c.391A>G (p.Thr131Ala)	NCK1 (T67A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2396131	NM_001291999.2(NCK1):c.433C>T (p.Arg145Cys)	NCK1 (R145C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2280126	NM_001291999.2(NCK1):c.496A>G (p.Ser166Gly)	NCK1 (S102G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2477241	NM_001291999.2(NCK1):c.512A>G (p.His171Arg)	NCK1 (H171R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3182242	NM_001291999.2(NCK1):c.554A>C (p.Asn185Thr)	NCK1 (N121T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3298764	NM_001291999.2(NCK1):c.620A>C (p.Glu207Ala)	NCK1 (E143A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2327036	NM_001291999.2(NCK1):c.817C>T (p.Leu273Phe)	IL20RB-AS1, NCK1 (L273F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2382990	NM_001291999.2(NCK1):c.955G>A (p.Val319Ile)	IL20RB-AS1, NCK1 (V255I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3182250	NM_001291999.2(NCK1):c.973G>A (p.Gly325Arg)	IL20RB-AS1, NCK1 (G325R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3182255	NM_001291999.2(NCK1):c.999A>T (p.Gln333His)	IL20RB-AS1, NCK1 (Q269H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2340182	NM_001291999.2(NCK1):c.1045A>T (p.Met349Leu)	IL20RB-AS1, NCK1 (M285L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2547676	NM_001291999.2(NCK1):c.1061A>G (p.Glu354Gly)	IL20RB-AS1, NCK1 (E290G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance