ClinVar Miner

List of variants in gene BCAP31 reported as uncertain significance for Inborn genetic diseases

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_001256447.2(BCAP31):c.119T>C (p.Leu40Pro)	rs1057518852
NM_001256447.2(BCAP31):c.493G>A (p.Gly165Arg)

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