Related gene-specific medical variations for Gene (Select 79870) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3259618	NM_024812.3(BAALC):c.104C>T (p.Ala35Val)	BAALC, BAALC-AS2 (A35V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3132738	NM_024812.3(BAALC):c.61C>G (p.Arg21Gly)	BAALC, BAALC-AS2 (R21G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2602493	NM_024812.3(BAALC):c.26A>T (p.Asp9Val)	BAALC, BAALC-AS2 +1 more (D9V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2489687	NM_024812.3(BAALC):c.40C>G (p.Arg14Gly)	BAALC, BAALC-AS2 +1 more (R14G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2333909	NM_024812.3(BAALC):c.125C>G (p.Pro42Arg)	BAALC, BAALC-AS2 (P42R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2208811	NM_024812.3(BAALC):c.54C>G (p.Ser18Arg)	BAALC, BAALC-AS2 (S18R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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