C3150275[trait identifier] AND "Fulgent Genetics, Fulgent Genetics"[su - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 906982	NM_000063.6(C2):c.749C>G (p.Ser250Cys)	C2 (S221C +2 more)	Single nucleotide variant (missense variant +1 more)	Complement component 2 deficiency +2 more	GUncertain significance
Select item 50634	NM_000063.6(C2):c.841_849+19del	C2 (V281fs)	Deletion (frameshift variant +2 more)	C2-related disorder +3 more	GConflicting classifications of pathogenicity
Select item 12130	NM_000063.6(C2):c.954G>C (p.Glu318Asp)	C2, C2-AS1 (E318D +3 more)	Single nucleotide variant (missense variant +1 more)	Complement component 2 deficiency +3 more	GBenign/Likely benign
Select item 1165861	NM_000063.6(C2):c.1567+22_1567+43del	C2	Deletion (intron variant)	not provided +2 more	GBenign/Likely benign
Select item 356258	NM_000063.6(C2):c.2046A>G (p.Ala682=)	C2, CFB	Single nucleotide variant (synonymous variant)	not provided +5 more	GBenign/Likely benign
Select item 16077	NM_001710.6(CFB):c.26T>A (p.Leu9His)	C2, CFB (L9H)	Single nucleotide variant (missense variant)	not provided +8 more	GBenign/Likely benign
Select item 16076	NM_001710.5(CFB):c.94C>T (p.Arg32Trp)	C2, CFB (R32W)	Single nucleotide variant (missense variant)	not provided +8 more	GBenign/Likely benign
Select item 16075	NM_001710.5(CFB):c.95G>A (p.Arg32Gln)	C2, CFB (R32Q)	Single nucleotide variant (missense variant)	not provided +7 more	GBenign/Likely benign
Select item 356284	NM_001710.6(CFB):c.1137C>T (p.Arg379=)	C2, CFB	Single nucleotide variant (synonymous variant)	Atypical hemolytic-uremic syndrome with B factor anomaly +9 more	GBenign/Likely benign
Select item 225313	NM_001710.6(CFB):c.1598A>G (p.Lys533Arg)	C2, CFB (K533R)	Single nucleotide variant (missense variant)	Age related macular degeneration 14 +7 more	GBenign/Likely benign