"Ambry Genetics"[submitter] AND "IL20RB-AS1"[gene] - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
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
Select item 2513526	NM_144717.4(IL20RB):c.176C>T (p.Ala59Val)	IL20RB, IL20RB-AS1 (A59V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3109299	NM_144717.4(IL20RB):c.205G>A (p.Glu69Lys)	IL20RB, IL20RB-AS1 (E69K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2595824	NM_144717.4(IL20RB):c.236C>T (p.Thr79Met)	IL20RB, IL20RB-AS1 (T79M)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign