"PreventionGenetics, part of Exact Sciences"[submitter] AND "ACOT7"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3055694	NM_007274.4(ACOT7):c.1023C>T (p.Thr341=)	ACOT7	Single nucleotide variant (synonymous variant)	ACOT7-related disorder	GBenign
Select item 3048989	NM_007274.4(ACOT7):c.384G>A (p.Val128=)	ACOT7	Single nucleotide variant (synonymous variant)	ACOT7-related disorder	GBenign
Select item 3039510	NM_007274.4(ACOT7):c.306C>T (p.Phe102=)	ACOT7	Single nucleotide variant (synonymous variant)	ACOT7-related disorder	GLikely benign
Select item 3041235	NM_007274.4(ACOT7):c.144-8956C>T	ACOT7, LOC129929234	Single nucleotide variant (intron variant)	ACOT7-related disorder	GBenign
Select item 3034269	NM_007274.4(ACOT7):c.144-10787G>A	ACOT7	Single nucleotide variant (5 prime UTR variant +1 more)	ACOT7-related disorder	GLikely benign
Select item 3048654	NM_007274.4(ACOT7):c.143+7755T>C	ACOT7	Single nucleotide variant (synonymous variant +1 more)	ACOT7-related disorder	GLikely benign

ClinVar