Related gene-specific medical variations for Gene (Select 89122) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3182433	NM_033091.3(TRIM4):c.247C>A (p.Pro83Thr)	LOC129998885, TRIM4 (P83T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2616208	NM_033091.3(TRIM4):c.164C>T (p.Pro55Leu)	LOC129998885, TRIM4 (P55L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2552785	NM_033091.3(TRIM4):c.209T>C (p.Leu70Pro)	LOC129998885, TRIM4 (L70P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2535706	NM_033091.3(TRIM4):c.295G>A (p.Glu99Lys)	LOC129998885, TRIM4 (E99K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2465630	NM_033091.3(TRIM4):c.197C>T (p.Ala66Val)	LOC129998885, TRIM4 (A66V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2317076	NM_033091.3(TRIM4):c.233G>C (p.Arg78Pro)	LOC129998885, TRIM4 (R78P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar