"Ambry Genetics"[submitter] AND "TRIM7-AS2"[gene] - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2477881	NM_203293.3(TRIM7):c.1499T>C (p.Val500Ala)	TRIM7, TRIM7-AS2 (V318A +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2298293	NM_203293.3(TRIM7):c.1472A>G (p.Gln491Arg)	TRIM7, TRIM7-AS2 (Q309R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2522404	NM_203293.3(TRIM7):c.1462G>A (p.Val488Ile)	TRIM7, TRIM7-AS2 (V280I +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3182780	NM_203293.3(TRIM7):c.1454C>T (p.Thr485Ile)	TRIM7, TRIM7-AS2 (T303I +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2467991	NM_203293.3(TRIM7):c.1418C>T (p.Ser473Phe)	TRIM7, TRIM7-AS2 (S265F +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3182779	NM_203293.3(TRIM7):c.1360A>C (p.Ser454Arg)	TRIM7, TRIM7-AS2 (S246R +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2516522	NM_203293.3(TRIM7):c.1304T>A (p.Leu435Gln)	TRIM7, TRIM7-AS2 (L435Q +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2606271	NM_203293.3(TRIM7):c.1187G>C (p.Arg396Pro)	TRIM7, TRIM7-AS2 (R214P +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3182777	NM_203293.3(TRIM7):c.1112A>G (p.Gln371Arg)	TRIM7, TRIM7-AS2 (Q371R +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2528517	NM_203293.3(TRIM7):c.1106G>C (p.Arg369Pro)	TRIM7, TRIM7-AS2 (R161P +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2529534	NM_203293.3(TRIM7):c.1090G>T (p.Val364Leu)	TRIM7, TRIM7-AS2 (V156L +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance