"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "ADAMTS9"[g - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2209821	NM_182920.2(ADAMTS9):c.4811G>A (p.Arg1604His)	ADAMTS9 (R1576H +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2653945	NM_182920.2(ADAMTS9):c.4716C>T (p.Gly1572=)	ADAMTS9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 774301	NM_182920.2(ADAMTS9):c.4356+4C>T	ADAMTS9	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 2653946	NM_182920.2(ADAMTS9):c.3591T>C (p.Thr1197=)	ADAMTS9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1879584	NM_182920.2(ADAMTS9):c.3525G>C (p.Arg1175Ser)	ADAMTS9 (R1147S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 770704	NM_182920.2(ADAMTS9):c.3475-7C>T	ADAMTS9	Single nucleotide variant (intron variant)	ADAMTS9-related condition +1 more	GBenign/Likely benign
Select item 2653947	NM_182920.2(ADAMTS9):c.3396G>A (p.Val1132=)	ADAMTS9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 707887	NM_182920.2(ADAMTS9):c.3102C>T (p.Asp1034=)	ADAMTS9	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 2653948	NM_182920.2(ADAMTS9):c.2475T>C (p.Ala825=)	ADAMTS9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2055165	NM_182920.2(ADAMTS9):c.846C>T (p.His282=)	ADAMTS9	Single nucleotide variant (synonymous variant)	ADAMTS9-related condition +1 more	GLikely benign
Select item 1344640	NM_182920.2(ADAMTS9):c.194C>G (p.Thr65Arg)	ADAMTS9, ADAMTS9-AS2 (T65R)	Single nucleotide variant (missense variant)	not provided	GConflicting classifications of pathogenicity