"Fulgent Genetics, Fulgent Genetics"[submitter] AND "COQ8B"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 385429	NM_024876.4(COQ8B):c.*10T>C	COQ8B	Single nucleotide variant (3 prime UTR variant)	Nephrotic syndrome, type 9 +1 more	GBenign/Likely benign
Select item 385863	NM_024876.4(COQ8B):c.1210-10G>A	COQ8B	Single nucleotide variant (intron variant)	Nephrotic syndrome, type 9 +2 more	GBenign/Likely benign
Select item 1315533	NM_024876.4(COQ8B):c.953C>T (p.Thr318Met)	COQ8B (T277M +1 more)	Single nucleotide variant (missense variant)	Nephrotic syndrome, type 9 +1 more	GUncertain significance

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