"Ambry Genetics"[submitter] AND "LOC126862066"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2272722	NM_006035.4(CDC42BPB):c.3796G>C (p.Glu1266Gln)	CDC42BPB, LOC126862066 (E1240Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2359760	NM_006035.4(CDC42BPB):c.3784C>T (p.Leu1262Phe)	CDC42BPB, LOC126862066 (L1262F +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign