Related gene-specific medical variations for Gene (Select 84458) - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2640730	NM_001346516.2(LCOR):c.2811T>G (p.Ala937=)	C10orf12, LCOR	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2399096	NM_001346516.2(LCOR):c.4454C>T (p.Ser1485Phe)	LCOR, C10orf12 (S1485F)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2343685	NM_001346516.2(LCOR):c.2308A>G (p.Ile770Val)	LCOR, C10orf12 (I770V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2260285	NM_001346516.2(LCOR):c.1783C>T (p.Pro595Ser)	C10orf12, LCOR (P595S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2258538	NM_001346516.2(LCOR):c.3872A>G (p.Glu1291Gly)	C10orf12, LCOR (E1291G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2253074	NM_001346516.2(LCOR):c.1438A>G (p.Thr480Ala)	LCOR, C10orf12 (T480A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2240353	NM_001346516.2(LCOR):c.4547G>A (p.Ser1516Asn)	C10orf12, LCOR (S1516N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2238969	NM_001346516.2(LCOR):c.4171C>A (p.Pro1391Thr)	C10orf12, LCOR (P1391T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2234530	NM_001346516.2(LCOR):c.3950G>A (p.Arg1317Gln)	C10orf12, LCOR (R1317Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2231979	NM_001346516.2(LCOR):c.4244C>A (p.Pro1415His)	LCOR, C10orf12 (P1415H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2211270	NM_001346516.2(LCOR):c.2912A>C (p.Asp971Ala)	C10orf12, LCOR (D971A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 219346	NM_001346516.2(LCOR):c.2564G>A (p.Arg855His)	C10orf12, LCOR (R855H)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance