"Ambry Genetics"[submitter] AND "LOC130065239"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2373521	NM_005762.3(TRIM28):c.95G>T (p.Arg32Leu)	LOC130065239, TRIM28 (R32L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2294606	NM_005762.3(TRIM28):c.119C>G (p.Ala40Gly)	LOC130065239, TRIM28 (A40G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2347242	NM_005762.3(TRIM28):c.130G>C (p.Ala44Pro)	LOC130065239, TRIM28 (A44P)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2329138	NM_005762.3(TRIM28):c.137C>T (p.Ala46Val)	LOC130065239, TRIM28 (A46V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2540623	NM_005762.3(TRIM28):c.140C>T (p.Ala47Val)	LOC130065239, TRIM28 (A47V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3182335	NM_005762.3(TRIM28):c.155C>G (p.Ala52Gly)	LOC130065239, TRIM28 (A52G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2535218	NM_005762.3(TRIM28):c.287C>T (p.Ala96Val)	LOC130065239, TRIM28 (A96V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3182338	NM_005762.3(TRIM28):c.323C>T (p.Ala108Val)	LOC130065239, TRIM28 (A108V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar