ACOT13[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3137632	NM_018473.4(ACOT13):c.45G>A (p.Met15Ile)	ACOT13 (M15I)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2470465	NM_018473.4(ACOT13):c.45G>T (p.Met15Ile)	ACOT13 (M15I)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3137607	NM_018473.4(ACOT13):c.175T>G (p.Leu59Val)	ACOT13 (L59V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3137610	NM_018473.4(ACOT13):c.176T>G (p.Leu59Trp)	ACOT13 (L36W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2456284	NM_018473.4(ACOT13):c.185C>T (p.Thr62Met)	ACOT13 (T62M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2514319	NM_018473.4(ACOT13):c.299T>C (p.Ile100Thr)	ACOT13 (I100T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3261910	NM_018473.4(ACOT13):c.300A>G (p.Ile100Met)	ACOT13 (I100M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2336963	NM_018473.4(ACOT13):c.316G>C (p.Val106Leu)	ACOT13 (V83L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2251962	NM_018473.4(ACOT13):c.341C>A (p.Ala114Glu)	ACOT13 (A114E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2532081	NM_018473.4(ACOT13):c.406A>G (p.Lys136Glu)	ACOT13 (K113E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance