ClinVar Miner

List of variants in gene SF3B1 reported as likely pathogenic for Hepatocellular carcinoma

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_012433.4(SF3B1):c.1996A>C (p.Lys666Gln)	rs754688962	0.00001
NM_012433.4(SF3B1):c.1996A>G (p.Lys666Glu)	rs754688962

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