"Ambry Genetics"[submitter] AND "ITGA9-AS1"[gene] - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2324263	NM_002207.3(ITGA9):c.2582C>T (p.Pro861Leu)	ITGA9, ITGA9-AS1 (P861L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2322434	NM_002207.3(ITGA9):c.2614A>G (p.Asn872Asp)	ITGA9, ITGA9-AS1 (N872D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2558767	NM_002207.3(ITGA9):c.2662G>A (p.Val888Ile)	ITGA9, ITGA9-AS1 (V888I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2608420	NM_002207.3(ITGA9):c.2814G>A (p.Met938Ile)	ITGA9, ITGA9-AS1 (M938I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3286752	NM_002207.3(ITGA9):c.2821G>A (p.Ala941Thr)	ITGA9, ITGA9-AS1 (A941T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2469010	NM_002207.3(ITGA9):c.2850G>C (p.Arg950Ser)	ITGA9, ITGA9-AS1 (R950S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2388727	NM_002207.3(ITGA9):c.2888C>T (p.Thr963Met)	ITGA9, ITGA9-AS1 (T963M)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2233065	NM_002207.3(ITGA9):c.2973C>G (p.Ile991Met)	ITGA9, ITGA9-AS1 (I991M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2347764	NM_002207.3(ITGA9):c.3061C>T (p.Arg1021Trp)	ITGA9, ITGA9-AS1 (R1021W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance