"Ambry Genetics"[submitter] AND "LOC126805642"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3330698	NM_020765.3(UBR4):c.9713G>A (p.Arg3238His)	LOC126805642, UBR4 (R3238H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2221603	NM_020765.3(UBR4):c.9709G>A (p.Val3237Met)	LOC126805642, UBR4 (V3237M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance