C4084709[trait identifier] AND "Fulgent Genetics, Fulgent Genetics"[su - ClinVar

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Items: 24

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 454188	NM_000245.4(MET):c.142G>A (p.Ala48Thr)	MET (A48T)	Single nucleotide variant (missense variant +1 more)	Autosomal recessive nonsyndromic hearing loss 97 +6 more	GConflicting classifications of pathogenicity
Select item 411909	NM_000245.4(MET):c.143C>G (p.Ala48Gly)	MET (A48G)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +5 more	GConflicting classifications of pathogenicity
Select item 142059	NM_000245.4(MET):c.406G>A (p.Val136Ile)	MET (V136I)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +8 more	GConflicting classifications of pathogenicity
Select item 824911	NM_000245.4(MET):c.446A>G (p.Asn149Ser)	MET (N149S)	Single nucleotide variant (missense variant +1 more)	Hepatocellular carcinoma +5 more	GUncertain significance
Select item 568449	NM_000245.4(MET):c.762A>C (p.Glu254Asp)	MET (E254D)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +6 more	GConflicting classifications of pathogenicity
Select item 411894	NM_000245.4(MET):c.799G>A (p.Glu267Lys)	MET (E267K)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +6 more	GUncertain significance
Select item 485734	NM_000245.4(MET):c.818C>A (p.Thr273Asn)	MET (T273N)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +6 more	GConflicting classifications of pathogenicity
Select item 41629	NM_000245.4(MET):c.948A>G (p.Ile316Met)	MET (I316M)	Single nucleotide variant (missense variant +1 more)	not specified +7 more	GBenign/Likely benign
Select item 185606	NM_000245.4(MET):c.1081G>T (p.Ala361Ser)	MET (A361S)	Single nucleotide variant (missense variant +1 more)	Autosomal recessive nonsyndromic hearing loss 97 +6 more	GConflicting classifications of pathogenicity
Select item 524881	NM_000245.4(MET):c.1157T>G (p.Leu386Arg)	MET (L386R)	Single nucleotide variant (missense variant +1 more)	Osteofibrous dysplasia +5 more	GUncertain significance
Select item 358684	NM_000245.4(MET):c.1174C>A (p.Pro392Thr)	MET (P392T)	Single nucleotide variant (missense variant +1 more)	Renal cell carcinoma +6 more	GUncertain significance
Select item 252899	NM_000245.4(MET):c.1336A>G (p.Ile446Val)	MET (I446V +1 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +6 more	GConflicting classifications of pathogenicity
Select item 216498	NM_000245.4(MET):c.1444G>A (p.Asp482Asn)	MET (D482N +1 more)	Single nucleotide variant (missense variant)	not provided +6 more	GUncertain significance
Select item 184358	NM_000245.4(MET):c.1669A>G (p.Thr557Ala)	MET (T557A +1 more)	Single nucleotide variant (missense variant)	Papillary renal cell carcinoma type 1 +7 more	GConflicting classifications of pathogenicity
Select item 524880	NM_000245.4(MET):c.1862C>T (p.Thr621Ile)	MET (T621I +1 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma +7 more	GConflicting classifications of pathogenicity
Select item 411891	NM_000245.4(MET):c.1933G>A (p.Gly645Arg)	MET (G645R +1 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma +6 more	GUncertain significance
Select item 411899	NM_000245.4(MET):c.2191C>T (p.Arg731Ter)	MET (R731* +1 more)	Single nucleotide variant (nonsense)	Renal cell carcinoma +5 more	GUncertain significance
Select item 524868	NM_000245.4(MET):c.2375A>G (p.His792Arg)	MET (H810R +2 more)	Single nucleotide variant (missense variant)	Osteofibrous dysplasia +5 more	GConflicting classifications of pathogenicity
Select item 219422	NM_000245.4(MET):c.2555T>A (p.Met852Lys)	MET (M870K +2 more)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +7 more	GConflicting classifications of pathogenicity
Select item 454219	NM_000245.4(MET):c.2684C>T (p.Thr895Met)	MET (T913M +2 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma +6 more	GConflicting classifications of pathogenicity
Select item 1480925	NM_000245.4(MET):c.2893G>A (p.Gly965Ser)	MET (G535S +2 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma +5 more	GUncertain significance
Select item 524889	NM_000245.4(MET):c.4034T>C (p.Ile1345Thr)	MET (I1363T +2 more)	Single nucleotide variant (missense variant)	not specified +7 more	GConflicting classifications of pathogenicity
Select item 485750	NM_000245.4(MET):c.4090C>T (p.Pro1364Ser)	MET (P1382S +2 more)	Single nucleotide variant (missense variant)	Osteofibrous dysplasia +6 more	GUncertain significance
Select item 971936	NM_000245.4(MET):c.4122C>A (p.Asn1374Lys)	MET (N1392K +2 more)	Single nucleotide variant (missense variant)	Renal cell carcinoma +6 more	GConflicting classifications of pathogenicity

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Items: 24