Related gene-specific medical variations for Gene (Select 51703) - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3262947	NM_203379.2(ACSL5):c.1678A>C (p.Asn560His)	ACSL5, ZDHHC6 (N616H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3262924	NM_203379.2(ACSL5):c.1723G>A (p.Gly575Arg)	ACSL5, ZDHHC6 (G631R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3262898	NM_203379.2(ACSL5):c.2003A>G (p.Lys668Arg)	ACSL5, ZDHHC6 (K700R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3140065	NM_203379.2(ACSL5):c.1972A>C (p.Thr658Pro)	ACSL5, ZDHHC6 (T658P +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3140049	NM_203379.2(ACSL5):c.1735C>T (p.Arg579Trp)	ACSL5, ZDHHC6 (R635W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3140043	NM_203379.2(ACSL5):c.1673T>C (p.Ile558Thr)	ACSL5, ZDHHC6 (I614T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2529585	NM_203379.2(ACSL5):c.1814C>T (p.Ser605Phe)	ACSL5, ZDHHC6 (S661F +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2396424	NM_203379.2(ACSL5):c.1729A>C (p.Ser577Arg)	ACSL5, ZDHHC6 (S577R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2336692	NM_203379.2(ACSL5):c.1784C>T (p.Ser595Leu)	ACSL5, ZDHHC6 (S595L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2233770	NM_203379.2(ACSL5):c.1613T>C (p.Ile538Thr)	ACSL5, ZDHHC6 (I538T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance