C10orf95-AS1[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 57116	GRCh38/hg38 10q23.33-25.3(chr10:95112607-116776637)x3	LOC130004500, LOC130004501 +821 more	Copy number gain	See cases	GPathogenic
Select item 59707	GRCh38/hg38 10q24.31-26.3(chr10:100194215-132432797)x3	EDRF1-AS1, EDRF1-DT +1036 more	Copy number gain	See cases	GPathogenic
Select item 148679	GRCh38/hg38 10q24.31-26.3(chr10:100600492-133622588)x3	GSTO1, GSTO2 +1097 more	Copy number gain	See cases	GPathogenic
Select item 58780	GRCh38/hg38 10q24.32-24.33(chr10:102243341-103929730)x1	ACTR1A, ARL3 +121 more	Copy number loss	See cases	GPathogenic
Select item 3572	NC_000010.11:g.(102444036_?)_(?_104726221)del	ACTR1A, ARL3 +135 more	Deletion	Desmoplastic/nodular medulloblastoma	GPathogenic
Select item 2376406	NM_001363580.1(C10orf95):c.507G>A (p.Gln169=)	C10orf95, C10orf95-AS1 +1 more	Single nucleotide variant (synonymous variant)	not specified	GUncertain significance
Select item 2207209	NM_001363580.1(C10orf95):c.440G>A (p.Arg147His)	C10orf95, C10orf95-AS1 +1 more (R147H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2404578	NM_001363580.1(C10orf95):c.410T>C (p.Leu137Pro)	C10orf95, C10orf95-AS1 +1 more (L137P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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