C0025267[trait identifier] AND "Fulgent Genetics, Fulgent Genetics"[su - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 13951	NM_020975.6(RET):c.2671T>G (p.Ser891Ala)	RET (S891A +17 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 2 +10 more	GPathogenic
Select item 305308	NM_001370259.2(MEN1):c.*302C>T	MEN1	Single nucleotide variant (3 prime UTR variant)	Multiple endocrine neoplasia, type 1 +2 more	GBenign/Likely benign
Select item 136166	NM_001370259.2(MEN1):c.1508G>A (p.Gly503Asp)	MEN1 (G503D +3 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GBenign/Likely benign
Select item 220268	NM_001370259.2(MEN1):c.1166G>A (p.Arg389Gln)	MEN1 (R394Q +3 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GConflicting classifications of pathogenicity
Select item 485711	NM_001370259.2(MEN1):c.941G>A (p.Arg314Gln)	MEN1 (R314Q +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 403812	NM_001370259.2(MEN1):c.883C>T (p.Arg295Trp)	MEN1 (R300W +2 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1 +2 more	GUncertain significance
Select item 216819	NM_001370259.2(MEN1):c.803A>G (p.Tyr268Cys)	MEN1 (Y268C +2 more)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia, type 1 +2 more	GConflicting classifications of pathogenicity
Select item 200972	NM_001370259.2(MEN1):c.473C>A (p.Ala158Asp)	MEN1 (A158D +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GConflicting classifications of pathogenicity
Select item 305317	NM_000244.4(MEN1):c.-35A>T	MEN1	Single nucleotide variant (5 prime UTR variant +1 more)	not specified +3 more	GBenign