Related gene-specific medical variations for Gene (Select 254251) - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3290312	NM_001394446.1(LCORL):c.32C>T (p.Ala11Val)	LCORL, LOC129992313 (A11V)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3181319	NM_022346.5(NCAPG):c.2882G>A (p.Arg961Lys)	LCORL, NCAPG (R961K)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3181316	NM_022346.5(NCAPG):c.2872G>C (p.Val958Leu)	LCORL, NCAPG (V958L)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3118150	NM_001394446.1(LCORL):c.69G>C (p.Gln23His)	LCORL, LOC129992313 (Q23H)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2472843	NM_022346.5(NCAPG):c.2971C>T (p.Pro991Ser)	LCORL, NCAPG (P991S)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2368312	NM_022346.5(NCAPG):c.2914G>A (p.Asp972Asn)	LCORL, NCAPG (D972N)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2362447	NM_001394446.1(LCORL):c.38C>T (p.Ala13Val)	LCORL, LOC129992313 (A13V)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2307067	NM_001394446.1(LCORL):c.41C>T (p.Ala14Val)	LCORL, LOC129992313 (A14V)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2257461	NM_001394446.1(LCORL):c.4G>A (p.Asp2Asn)	LCORL, LOC129992313 (D2N)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2213599	NM_022346.5(NCAPG):c.2980G>A (p.Ala994Thr)	LCORL, NCAPG (A994T)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance