"Ambry Genetics"[submitter] AND "LOC126861119"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3182558	NM_033034.3(TRIM5):c.508T>C (p.Trp170Arg)	LOC126861119, TRIM5 (W170R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3328807	NM_033034.3(TRIM5):c.449G>A (p.Arg150Lys)	LOC126861119, TRIM5 (R150K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2261861	NM_033034.3(TRIM5):c.400G>A (p.Val134Ile)	LOC126861119, TRIM5 (V134I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2367199	NM_033034.3(TRIM5):c.284G>C (p.Cys95Ser)	LOC126861119, TRIM5 (C95S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2387443	NM_033034.3(TRIM5):c.212G>A (p.Arg71Gln)	LOC126861119, TRIM5 (R71Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2211378	NM_033034.3(TRIM5):c.211C>T (p.Arg71Trp)	LOC126861119, TRIM5 (R71W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar