List of variants in gene BRCA1 reported as likely benign by Cancer Genetics and Genomics Laboratory, British Columbia Cancer Agency

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_007294.4(BRCA1):c.1036C>T (p.Pro346Ser)	rs80357015	0.00032
NM_007294.4(BRCA1):c.5332+13G>T	rs372391060	0.00007
NM_007294.4(BRCA1):c.1392C>T (p.Thr464=)	rs533802049	0.00006
NM_007294.4(BRCA1):c.795T>C (p.Ser265=)	rs201441987	0.00006
NM_007294.4(BRCA1):c.199G>T (p.Asp67Tyr)	rs80357102	0.00005
NM_007294.4(BRCA1):c.36A>G (p.Gln12=)	rs763230080	0.00004
NM_007294.4(BRCA1):c.396C>A (p.Asn132Lys)	rs80357413	0.00003
NM_007294.4(BRCA1):c.5310G>A (p.Gly1770=)	rs273901761	0.00003
NM_007294.4(BRCA1):c.154C>T (p.Leu52Phe)	rs80357084	0.00001
NM_007294.4(BRCA1):c.886A>G (p.Arg296Gly)	rs748675395	0.00001
NM_007294.4(BRCA1):c.2177T>C (p.Leu726Pro)	rs1135401827
NM_007294.4(BRCA1):c.426C>T (p.Pro142=)	rs542687218
NM_007294.4(BRCA1):c.511A>G (p.Ile171Val)	rs777515082
NM_007294.4(BRCA1):c.823G>A (p.Gly275Ser)	rs8176153
NM_007294.4(BRCA1):c.889A>C (p.Met297Leu)	rs80357196

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