List of variants in gene BRIP1 reported as likely benign for Hereditary cancer

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_032043.3(BRIP1):c.2220G>T (p.Gln740His)	rs45589637	0.00041
NM_032043.3(BRIP1):c.728T>C (p.Ile243Thr)	rs587781860	0.00003
NM_032043.3(BRIP1):c.1014A>G (p.Glu338=)	rs1490732516
NM_032043.3(BRIP1):c.3275C>A (p.Pro1092Gln)	rs587780830
NM_032043.3(BRIP1):c.3651G>T (p.Trp1217Cys)	rs542698396
NM_032043.3(BRIP1):c.588C>G (p.Asn196Lys)	rs758851721

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