"Fulgent Genetics, Fulgent Genetics"[submitter] AND "LOC130006895"[gen - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 488171	NM_005188.4(CBL):c.93C>A (p.Asp31Glu)	CBL, LOC130006895 (D31E)	Single nucleotide variant (missense variant)	RASopathy +3 more	GUncertain significance
Select item 40400	NM_005188.4(CBL):c.107ACC[8] (p.His42dup)	CBL, LOC130006895	Microsatellite (inframe_insertion)	not specified +7 more	GBenign/Likely benign
Select item 180808	NM_005188.4(CBL):c.107ACC[6] (p.His42del)	CBL, LOC130006895 (H42del)	Microsatellite (inframe_deletion)	Juvenile myelomonocytic leukemia +2 more	GBenign/Likely benign

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ClinVar