List of variants in gene BRIP1 reported as uncertain significance by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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)
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_032043.3(BRIP1):c.1735C>T (p.Arg579Cys)	rs28997571	0.00034
NM_032043.3(BRIP1):c.139C>G (p.Pro47Ala)	rs28903098	0.00024
NM_032043.3(BRIP1):c.3444C>A (p.Asp1148Glu)	rs28997573	0.00011
NM_032043.3(BRIP1):c.2087C>T (p.Pro696Leu)	rs147755155	0.00006
NM_032043.3(BRIP1):c.3103C>T (p.Arg1035Cys)	rs45437094	0.00006
NM_032043.3(BRIP1):c.413T>C (p.Leu138Ser)	rs587780251	0.00006
NM_032043.3(BRIP1):c.2563C>T (p.Arg855Cys)	rs146031731	0.00004
NM_032043.3(BRIP1):c.1754C>A (p.Ala585Glu)	rs756946068	0.00001
NM_032043.3(BRIP1):c.1873T>C (p.Ser625Pro)	rs935011040	0.00001
NM_032043.3(BRIP1):c.2594G>A (p.Arg865Gln)	rs781609846	0.00001
NM_032043.3(BRIP1):c.3505G>T (p.Asp1169Tyr)	rs587782029	0.00001
NM_032043.3(BRIP1):c.1331G>C (p.Ser444Thr)	rs1603342140
NM_032043.3(BRIP1):c.1363T>C (p.Tyr455His)	rs587780826
NM_032043.3(BRIP1):c.629C>A (p.Pro210His)	rs140097800

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