"Ambry Genetics"[submitter] AND "TRIM6"[gene] - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2365787	NM_001003818.3(TRIM6):c.506A>G (p.Gln169Arg)	TRIM5, TRIM6 (Q141R +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2252667	NM_001003818.3(TRIM6):c.1007A>G (p.His336Arg)	TRIM5, TRIM6 (H133R +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2336194	NM_001003818.3(TRIM6):c.1025T>C (p.Leu342Pro)	TRIM5, TRIM6 (L139P +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2313514	NM_001003818.3(TRIM6):c.1084T>C (p.Ser362Pro)	TRIM6, TRIM5 (S159P +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2550021	NM_001003818.3(TRIM6):c.1158G>C (p.Glu386Asp)	TRIM5, TRIM6 (E183D +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2225468	NM_001003818.3(TRIM6):c.1185G>C (p.Trp395Cys)	TRIM6, TRIM5 (W367C +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2621634	NM_001003818.3(TRIM6):c.1271A>G (p.Gln424Arg)	TRIM5, TRIM6 (Q221R +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2248200	NM_001003818.3(TRIM6):c.1376G>A (p.Arg459His)	TRIM5, TRIM6 (R256H +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2532518	NM_001003818.3(TRIM6):c.1391T>C (p.Phe464Ser)	TRIM5, TRIM6 (F261S +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2316016	NM_001003818.3(TRIM6):c.1427A>C (p.Asn476Thr)	TRIM6, TRIM5 (N448T +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2376827	NM_001003818.3(TRIM6):c.1504C>A (p.Pro502Thr)	TRIM5, TRIM6 (P299T +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2215033	NM_001003818.3(TRIM6):c.1534C>T (p.Arg512Cys)	TRIM6, TRIM5 (R512C +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2394048	NM_001003818.3(TRIM6):c.1538G>A (p.Arg513His)	TRIM5, TRIM6 (R485H +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance