Related gene-specific medical variations for Gene (Select 101929335) - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2978260	NM_182920.2(ADAMTS9):c.4560G>A (p.Arg1520=)	ADAMTS9, ADAMTS9-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2614510	NM_182920.2(ADAMTS9):c.4513G>T (p.Ala1505Ser)	ADAMTS9, ADAMTS9-AS1 (A1505S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2594444	NM_182920.2(ADAMTS9):c.4496C>T (p.Pro1499Leu)	ADAMTS9, ADAMTS9-AS1 (P1499L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2377200	NM_182920.2(ADAMTS9):c.4579G>A (p.Gly1527Arg)	ADAMTS9-AS1, ADAMTS9 (G1499R +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 1909859	NM_182920.2(ADAMTS9):c.4467G>A (p.Gly1489=)	ADAMTS9, ADAMTS9-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1652674	NM_182920.2(ADAMTS9):c.4524+16C>T	ADAMTS9, ADAMTS9-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1535005	NM_182920.2(ADAMTS9):c.4562A>T (p.His1521Leu)	ADAMTS9-AS1, ADAMTS9 (H1493L +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1374698	NM_182920.2(ADAMTS9):c.4513G>A (p.Ala1505Thr)	ADAMTS9, ADAMTS9-AS1 (A1505T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1344639	NM_182920.2(ADAMTS9):c.4575_4576del (p.Gln1525fs)	ADAMTS9, ADAMTS9-AS1 (Q1497fs +1 more)	Deletion (non-coding transcript variant +1 more)	Nephronophthisis	GLikely pathogenic
Select item 1286160	NM_182920.2(ADAMTS9):c.4698+76A>G	ADAMTS9, ADAMTS9-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 1266838	NM_182920.2(ADAMTS9):c.4525-75G>A	ADAMTS9, ADAMTS9-AS1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1262649	NM_182920.2(ADAMTS9):c.4357-48C>T	ADAMTS9, ADAMTS9-AS1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1248560	NM_182920.2(ADAMTS9):c.4525-50C>G	ADAMTS9, ADAMTS9-AS1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1242995	NM_182920.2(ADAMTS9):c.4357-43A>G	ADAMTS9, ADAMTS9-AS1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1229313	NM_182920.2(ADAMTS9):c.4524+81A>G	ADAMTS9, ADAMTS9-AS1	Single nucleotide variant (intron variant)	not provided	GBenign