Related gene-specific medical variations for Gene (Select 27098) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2539741	NM_001393344.1(CLUL1):c.1204A>G (p.Ile402Val)	CLUL1, LOC126862676 (I402V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2521156	NM_001393344.1(CLUL1):c.1033G>A (p.Glu345Lys)	CLUL1, LOC126862676 (E345K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2234412	NM_001393344.1(CLUL1):c.1009C>A (p.Pro337Thr)	CLUL1, LOC126862676 (P337T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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