Related gene-specific medical variations for Gene (Select 2181) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3262851	NM_004457.5(ACSL3):c.761A>T (p.His254Leu)	ACSL3, ACSL3-AS1 (H254L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2594647	NM_004457.5(ACSL3):c.802A>G (p.Met268Val)	ACSL3, ACSL3-AS1 (M268V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 724724	NM_004457.5(ACSL3):c.794A>G (p.Lys265Arg)	ACSL3, ACSL3-AS1 (K265R)	Single nucleotide variant (missense variant)	not provided	GLikely benign

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