"Ambry Genetics"[submitter] AND "TRAT1"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3182060	NM_016388.4(TRAT1):c.139A>G (p.Ser47Gly)	TRAT1 (S10G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2495753	NM_016388.4(TRAT1):c.283G>C (p.Glu95Gln)	TRAT1 (E58Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3328557	NM_016388.4(TRAT1):c.296C>G (p.Ser99Cys)	TRAT1 (S99C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3182061	NM_016388.4(TRAT1):c.331G>A (p.Ala111Thr)	TRAT1 (A111T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3182062	NM_016388.4(TRAT1):c.438C>A (p.Ser146Arg)	TRAT1 (S109R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3182063	NM_016388.4(TRAT1):c.439G>A (p.Val147Ile)	TRAT1 (V147I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2301751	NM_016388.4(TRAT1):c.457G>A (p.Val153Ile)	TRAT1 (V116I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2545795	NM_016388.4(TRAT1):c.554T>C (p.Ile185Thr)	TRAT1 (I148T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar