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

Minimum submission review status:		Collection method:
Minimum conflict level:
Gene type:		Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 35

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HGVS	dbSNP
NM_007294.3(BRCA1):c.81-13C>G	rs56328013
NM_007294.4(BRCA1):c.*1113G>A	rs111791349
NM_007294.4(BRCA1):c.*1327G>A	rs184237074
NM_007294.4(BRCA1):c.*1332G>A	rs8176320
NM_007294.4(BRCA1):c.*750A>G	rs138782023
NM_007294.4(BRCA1):c.*781C>T	rs8176319
NM_007294.4(BRCA1):c.*873del	rs59541324
NM_007294.4(BRCA1):c.1487G>A (p.Arg496His)	rs28897677
NM_007294.4(BRCA1):c.1511G>A (p.Arg504His)	rs56272539
NM_007294.4(BRCA1):c.199G>T (p.Asp67Tyr)	rs80357102
NM_007294.4(BRCA1):c.21C>T (p.Arg7=)	rs149402012
NM_007294.4(BRCA1):c.2315T>C (p.Val772Ala)	rs80357467
NM_007294.4(BRCA1):c.2521C>T (p.Arg841Trp)	rs1800709
NM_007294.4(BRCA1):c.2596C>T (p.Arg866Cys)	rs41286300
NM_007294.4(BRCA1):c.2733A>G (p.Gly911=)	rs1800740
NM_007294.4(BRCA1):c.3024G>A (p.Met1008Ile)	rs1800704
NM_007294.4(BRCA1):c.314A>G (p.Tyr105Cys)	rs28897673
NM_007294.4(BRCA1):c.3296C>T (p.Pro1099Leu)	rs80357201
NM_007294.4(BRCA1):c.3418A>G (p.Ser1140Gly)	rs2227945
NM_007294.4(BRCA1):c.3713C>T (p.Pro1238Leu)	rs28897688
NM_007294.4(BRCA1):c.3748G>A (p.Glu1250Lys)	rs28897686
NM_007294.4(BRCA1):c.396C>A (p.Asn132Lys)	rs80357413
NM_007294.4(BRCA1):c.4032T>C (p.Asp1344=)
NM_007294.4(BRCA1):c.4113G>A (p.Gly1371=)	rs147448807
NM_007294.4(BRCA1):c.4358-10C>T	rs80358111
NM_007294.4(BRCA1):c.4484+14A>G	rs80358022
NM_007294.4(BRCA1):c.4636G>A (p.Asp1546Asn)	rs28897691
NM_007294.4(BRCA1):c.4682C>T (p.Thr1561Ile)	rs56158747
NM_007294.4(BRCA1):c.4956G>A (p.Met1652Ile)	rs1799967
NM_007294.4(BRCA1):c.5252G>A (p.Arg1751Gln)	rs80357442
NM_007294.4(BRCA1):c.5406+8T>C	rs55946644
NM_007294.4(BRCA1):c.571G>A (p.Val191Ile)	rs80357090
NM_007294.4(BRCA1):c.591C>T (p.Cys197=)	rs1799965
NM_007294.4(BRCA1):c.811G>A (p.Val271Met)	rs80357244
NM_007294.4(BRCA1):c.981A>G (p.Thr327=)	rs1800063

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