Related gene-specific medical variations for Gene (Select 56658) - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3182426	NM_001199119.1(TRIM39-RPP21):c.1031G>A (p.Arg344Lys)	TRIM39, TRIM39-RPP21 (R374K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3182425	NM_001369521.2(TRIM39):c.804-172C>T	LOC126859643, TRIM39 +1 more (L289F)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3182424	NM_001369521.2(TRIM39):c.1288A>G (p.Ile430Val)	TRIM39, TRIM39-RPP21 (I460V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2593543	NM_001369521.2(TRIM39):c.804-232A>C	TRIM39, TRIM39-RPP21 (N269H)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2535979	NM_001369521.2(TRIM39):c.1150G>A (p.Val384Met)	TRIM39, TRIM39-RPP21 (V384M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2339535	NM_001369521.2(TRIM39):c.804-187C>T	LOC126859643, TRIM39 +1 more (R284W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2317468	NM_001369521.2(TRIM39):c.1340G>A (p.Arg447His)	TRIM39, TRIM39-RPP21 (R447H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2293761	NM_001369521.2(TRIM39):c.804-226C>T	TRIM39, TRIM39-RPP21 (P271S)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2284796	NM_001369521.2(TRIM39):c.1441A>G (p.Ile481Val)	TRIM39, TRIM39-RPP21 (I481V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance