List of variants in gene BRCA1 reported as not provided by Breast Cancer Information Core (BIC) (BRCA1)

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: 32

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HGVS	dbSNP	gnomAD frequency
NM_007294.4(BRCA1):c.2082C>T (p.Ser694=)	rs1799949	0.30810
NM_007294.4(BRCA1):c.4987-68A>G	rs8176234	0.30809
NM_007294.4(BRCA1):c.4987-92A>G	rs8176233	0.30647
NM_007294.4(BRCA1):c.5152+66G>A	rs3092994	0.30314
NM_007294.4(BRCA1):c.4308T>C (p.Ser1436=)	rs1060915	0.29170
NM_007294.4(BRCA1):c.3113A>G (p.Glu1038Gly)	rs16941	0.29115
NM_007294.4(BRCA1):c.2311T>C (p.Leu771=)	rs16940	0.29035
NM_007294.4(BRCA1):c.442-34C>T	rs799923	0.15730
NM_007294.4(BRCA1):c.2814A>G (p.Pro938=)	rs80356851	0.00183
NM_007294.4(BRCA1):c.591C>T (p.Cys197=)	rs1799965	0.00117
NM_007294.4(BRCA1):c.-19-10T>C	rs201866997	0.00007
NM_007294.4(BRCA1):c.181T>G (p.Cys61Gly)	rs28897672	0.00004
NM_007294.4(BRCA1):c.5251C>T (p.Arg1751Ter)	rs80357123	0.00003
NM_007294.4(BRCA1):c.5531T>G (p.Leu1844Arg)	rs80357323	0.00002
NM_007294.4(BRCA1):c.135-1G>T	rs80358158	0.00001
NM_007294.4(BRCA1):c.1687C>T (p.Gln563Ter)	rs80356898	0.00001
NM_007294.4(BRCA1):c.212+3A>G	rs80358083	0.00001
NM_007294.4(BRCA1):c.4986+6T>C	rs80358086	0.00001
NM_007294.4(BRCA1):c.1016del (p.Lys339fs)	rs80357569
NM_007294.4(BRCA1):c.1204G>T (p.Glu402Ter)	rs273897655
NM_007294.4(BRCA1):c.2098_2099insA (p.Leu700fs)	rs483353086
NM_007294.4(BRCA1):c.2635G>T (p.Glu879Ter)	rs80357251
NM_007294.4(BRCA1):c.3112G>T (p.Glu1038Ter)	rs80357161
NM_007294.4(BRCA1):c.4372C>T (p.Gln1458Ter)	rs80356932
NM_007294.4(BRCA1):c.4656C>G (p.Tyr1552Ter)	rs80357151
NM_007294.4(BRCA1):c.470_471del (p.Leu156_Ser157insTer)	rs80357887
NM_007294.4(BRCA1):c.4837A>G (p.Ser1613Gly)	rs1799966
NM_007294.4(BRCA1):c.4986+6T>G	rs80358086
NM_007294.4(BRCA1):c.5406+1_5406+3del	rs397509277
NM_007294.4(BRCA1):c.5467G>A (p.Ala1823Thr)	rs80357212
NM_007294.4(BRCA1):c.962G>A (p.Trp321Ter)	rs80357292
NM_007294.4(BRCA1):c.981_982del (p.Thr327_Cys328insTer)	rs80357772

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