"PreventionGenetics, part of Exact Sciences"[submitter] AND "TAT"[gene - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 710399	NM_000353.3(TAT):c.929T>C (p.Val310Ala)	TAT, TAT-AS1 (V310A)	Single nucleotide variant (missense variant)	TAT-related disorder +1 more	GLikely benign
Select item 788246	NM_000353.3(TAT):c.804C>T (p.Thr268=)	TAT, TAT-AS1	Single nucleotide variant (synonymous variant)	Tyrosinemia type II +1 more	GBenign/Likely benign
Select item 1539587	NM_000353.3(TAT):c.531G>A (p.Glu177=)	LOC111413029, TAT	Single nucleotide variant (synonymous variant)	Tyrosinemia type II +1 more	GLikely benign
Select item 255935	NM_000353.3(TAT):c.309G>A (p.Ser103=)	TAT	Single nucleotide variant (synonymous variant)	Tyrosinemia type II +2 more	GBenign
Select item 2632212	NM_000353.3(TAT):c.170G>A (p.Arg57Gln)	TAT (R57Q)	Single nucleotide variant (missense variant)	TAT-related disorder	GUncertain significance

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