List of variants in gene BRCA1 reported as likely benign by Illumina Laboratory Services, Illumina

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: 30

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HGVS	dbSNP	gnomAD frequency
NM_007294.4(BRCA1):c.4956G>A (p.Met1652Ile)	rs1799967	0.01348
NM_007294.4(BRCA1):c.*1332G>A	rs8176320	0.01007
NM_007294.4(BRCA1):c.*781C>T	rs8176319	0.00732
NM_007294.4(BRCA1):c.5406+8T>C	rs55946644	0.00474
NM_007294.4(BRCA1):c.*1113G>A	rs111791349	0.00473
NM_007294.4(BRCA1):c.*750A>G	rs138782023	0.00424
NM_007294.4(BRCA1):c.21C>T (p.Arg7=)	rs149402012	0.00165
NM_007294.4(BRCA1):c.4682C>T (p.Thr1561Ile)	rs56158747	0.00150
NM_007294.4(BRCA1):c.2521C>T (p.Arg841Trp)	rs1800709	0.00137
NM_007294.4(BRCA1):c.4113G>A (p.Gly1371=)	rs147448807	0.00135
NM_007294.4(BRCA1):c.591C>T (p.Cys197=)	rs1799965	0.00117
NM_007294.4(BRCA1):c.*1327G>A	rs184237074	0.00099
NM_007294.4(BRCA1):c.2733A>G (p.Gly911=)	rs1800740	0.00066
NM_007294.4(BRCA1):c.981A>G (p.Thr327=)	rs1800063	0.00066
NM_007294.4(BRCA1):c.3024G>A (p.Met1008Ile)	rs1800704	0.00065
NM_007294.4(BRCA1):c.1487G>A (p.Arg496His)	rs28897677	0.00060
NM_007294.4(BRCA1):c.4484+14A>G	rs80358022	0.00036
NM_007294.4(BRCA1):c.4358-10C>T	rs80358111	0.00024
NM_007294.4(BRCA1):c.571G>A (p.Val191Ile)	rs80357090	0.00021
NM_007294.4(BRCA1):c.2315T>C (p.Val772Ala)	rs80357467	0.00012
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.199G>T (p.Asp67Tyr)	rs80357102	0.00006
NM_007294.4(BRCA1):c.4636G>A (p.Asp1546Asn)	rs28897691	0.00006
NM_007294.4(BRCA1):c.1511G>A (p.Arg504His)	rs56272539	0.00005
NM_007294.4(BRCA1):c.396C>A (p.Asn132Lys)	rs80357413	0.00003
NM_007294.4(BRCA1):c.5252G>A (p.Arg1751Gln)	rs80357442	0.00003
NM_007294.4(BRCA1):c.811G>A (p.Val271Met)	rs80357244	0.00003
NM_007294.4(BRCA1):c.*873del	rs59541324
NM_007294.4(BRCA1):c.81-13C>G	rs56328013

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