"PreventionGenetics, part of Exact Sciences"[submitter] AND "CRAT"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1166275	NM_000755.5(CRAT):c.1335C>T (p.Tyr445=)	CRAT	Single nucleotide variant (synonymous variant)	CRAT-related disorder +1 more	GBenign
Select item 2634781	NM_000755.5(CRAT):c.1162G>A (p.Glu388Lys)	CRAT (E348K +3 more)	Single nucleotide variant (missense variant)	CRAT-related disorder	GUncertain significance
Select item 741916	NM_000755.5(CRAT):c.1036G>A (p.Ala346Thr)	CRAT (A325T +3 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 1168217	NM_000755.5(CRAT):c.954C>T (p.Ser318=)	CRAT	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 1168369	NM_000755.5(CRAT):c.354G>C (p.Ser118=)	CRAT	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 617562	NM_000755.5(CRAT):c.329A>G (p.Tyr110Cys)	CRAT (Y110C +3 more)	Single nucleotide variant (missense variant)	CRAT-related disorder +1 more	GLikely benign
Select item 2747927	NM_000755.5(CRAT):c.159G>A (p.Ala53=)	CRAT	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign

ClinVar