"Ambry Genetics"[submitter] AND "LOC129936902"[gene] - ClinVar - NCBI

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Items: 3

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2409592	NM_001064.4(TKT):c.84G>T (p.Gln28His)	TKT, LOC129936902 (Q28H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2380978	NM_001064.4(TKT):c.73A>G (p.Ser25Gly)	LOC129936902, TKT (S25G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2521567	NM_001064.4(TKT):c.52A>G (p.Thr18Ala)	LOC129936902, TKT (T18A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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