List of variants in gene BRCA1 reported by Center of Medical Genetics and Primary Health Care

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_007294.4(BRCA1):c.3113A>G (p.Glu1038Gly)	rs16941	0.29115
NM_007294.4(BRCA1):c.1067A>G (p.Gln356Arg)	rs1799950	0.04695
NM_007294.4(BRCA1):c.4956G>A (p.Met1652Ile)	rs1799967	0.01348
NM_007294.4(BRCA1):c.5444G>A (p.Trp1815Ter)	rs80356962	0.00001
NM_007294.4(BRCA1):c.1504_1508del (p.Leu502fs)	rs80357888
NM_007294.4(BRCA1):c.211A>G (p.Arg71Gly)	rs80357382
NM_007294.4(BRCA1):c.2649_2650insGGCA (p.Thr884fs)	rs886038003
NM_007294.4(BRCA1):c.302-1G>A	rs80358116
NM_007294.4(BRCA1):c.4358-2A>G	rs1555582723
NM_007294.4(BRCA1):c.4837A>G (p.Ser1613Gly)	rs1799966
NM_007294.4(BRCA1):c.5191G>A (p.Glu1731Lys)	rs397507244
NM_007294.4(BRCA1):c.5360G>A (p.Cys1787Tyr)	rs1597801649
NM_007294.4(BRCA1):c.798_799del (p.Ser267fs)	rs80357724

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