C0018609[trait identifier] AND "Genetic Services Laboratory, Universit - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 130352	NM_001003841.3(SLC6A19):c.306T>C (p.Gly102=)	SLC6A19	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 2019	NM_001003841.3(SLC6A19):c.517G>A (p.Asp173Asn)	SLC6A19 (D173N)	Single nucleotide variant (missense variant)	Neutral 1 amino acid transport defect +5 more	GConflicting classifications of pathogenicity
Select item 130354	NM_001003841.3(SLC6A19):c.990A>G (p.Thr330=)	SLC6A19	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign

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