"Ambry Genetics"[submitter] AND "LOC126863144"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2209328	NM_001039141.3(TRIOBP):c.5326G>A (p.Asp1776Asn)	LOC126863144, TRIOBP (D1776N +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2068946	NM_001039141.3(TRIOBP):c.5367C>G (p.Asp1789Glu)	LOC126863144, TRIOBP (D76E +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance