List of variants in gene BRCA1 reported as benign 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: 27

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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.2077G>A (p.Asp693Asn)	rs4986850	0.05782
NM_007294.4(BRCA1):c.5406+8T>C	rs55946644	0.00514
NM_007294.4(BRCA1):c.4535G>T (p.Ser1512Ile)	rs1800744	0.00240
NM_007294.4(BRCA1):c.114G>A (p.Lys38=)	rs1800062	0.00233
NM_007294.4(BRCA1):c.1137T>G (p.Ile379Met)	rs56128296	0.00158
NM_007294.4(BRCA1):c.3022A>G (p.Met1008Val)	rs56321129	0.00095
NM_007294.4(BRCA1):c.4840C>T (p.Pro1614Ser)	rs70953660	0.00065
NM_007294.4(BRCA1):c.4691T>C (p.Leu1564Pro)	rs56119278	0.00059
NM_007294.4(BRCA1):c.4358-10C>T	rs80358111	0.00024
NM_007294.4(BRCA1):c.1065G>A (p.Lys355=)	rs41286292	0.00011
NM_007294.4(BRCA1):c.2596C>T (p.Arg866Cys)	rs41286300	0.00011
NM_007294.4(BRCA1):c.314A>G (p.Tyr105Cys)	rs28897673	0.00009
NM_007294.4(BRCA1):c.75C>T (p.Pro25=)	rs80356839	0.00004
NM_007294.4(BRCA1):c.1001C>T (p.Pro334Leu)	rs41286290	0.00002
NM_007294.4(BRCA1):c.4347A>G (p.Thr1449=)	rs80356840	0.00001
NM_007294.4(BRCA1):c.*106C>G	rs189442183
NM_007294.4(BRCA1):c.-19-32AT[7]	rs273898667
NM_007294.4(BRCA1):c.2077G>T (p.Asp693Tyr)	rs4986850
NM_007294.4(BRCA1):c.2356C>T (p.Leu786=)	rs483353087
NM_007294.4(BRCA1):c.2612C>T (p.Pro871Leu)	rs799917
NM_007294.4(BRCA1):c.4185+11TG[5]	rs273900723
NM_007294.4(BRCA1):c.5113C>T (p.Leu1705=)	rs80356858
NM_007294.4(BRCA1):c.548-56del	rs1567804371
NM_007294.4(BRCA1):c.548-58del	rs8176144
NM_007294.4(BRCA1):c.548-68del	rs273902773

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