"Ambry Genetics"[submitter] AND "TRIM9"[gene] - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2306259	NM_001387360.1(TRIM9):c.2195T>C (p.Ile732Thr)	TRIM9 (I530T +18 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2321348	NM_001387360.1(TRIM9):c.1580C>T (p.Thr527Ile)	TRIM9 (T454I +4 more)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2476774	NM_001387360.1(TRIM9):c.1559G>T (p.Gly520Val)	TRIM9 (G516V +4 more)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2339215	NM_001387360.1(TRIM9):c.1543G>T (p.Ala515Ser)	TRIM9 (A515S +4 more)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2261641	NM_001387360.1(TRIM9):c.1458A>C (p.Gln486His)	TRIM9 (Q449H +4 more)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2611391	NM_001387360.1(TRIM9):c.1414G>A (p.Ala472Thr)	TRIM9 (A399T +4 more)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2529065	NM_001387360.1(TRIM9):c.1208G>A (p.Gly403Asp)	TRIM9 (G366D +3 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2284502	NM_001387360.1(TRIM9):c.1201G>A (p.Gly401Ser)	TRIM9 (G364S +3 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2622823	NM_001387360.1(TRIM9):c.1007C>T (p.Ala336Val)	TRIM9 (A335V +1 more)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2321349	NM_001387360.1(TRIM9):c.925A>G (p.Ser309Gly)	TRIM9 (S308G +1 more)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2476684	NM_001387360.1(TRIM9):c.880T>C (p.Phe294Leu)	TRIM9 (F294L)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2389865	NM_001387360.1(TRIM9):c.847G>A (p.Gly283Arg)	TRIM9 (G283R)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2532632	NM_001387360.1(TRIM9):c.787G>C (p.Val263Leu)	TRIM9 (V263L)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2622283	NM_001387360.1(TRIM9):c.736A>G (p.Met246Val)	TRIM9 (M246V)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2219230	NM_001387360.1(TRIM9):c.622C>T (p.Arg208Cys)	TRIM9 (R208C)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2238949	NM_001387360.1(TRIM9):c.481A>G (p.Ser161Gly)	TRIM9 (S161G)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2486772	NM_001387360.1(TRIM9):c.386C>T (p.Pro129Leu)	TRIM9 (P129L)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2295871	NM_001387360.1(TRIM9):c.314C>T (p.Ala105Val)	TRIM9 (A105V)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance