List of variants in gene BRCA1 reported as likely benign by Institute for Biomarker Research, Medical Diagnostic Laboratories, L.L.C.

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: 29

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HGVS	dbSNP	gnomAD frequency
NM_007294.4(BRCA1):c.212+23T>A	rs8176128	0.01018
NM_007294.4(BRCA1):c.2458A>G (p.Lys820Glu)	rs56082113	0.00964
NM_007294.4(BRCA1):c.2167A>G (p.Asn723Asp)	rs4986845	0.00209
NM_007294.4(BRCA1):c.2814A>G (p.Pro938=)	rs80356851	0.00183
NM_007294.4(BRCA1):c.4682C>T (p.Thr1561Ile)	rs56158747	0.00150
NM_007294.4(BRCA1):c.3083G>A (p.Arg1028His)	rs80357459	0.00106
NM_007294.4(BRCA1):c.3024G>A (p.Met1008Ile)	rs1800704	0.00065
NM_007294.4(BRCA1):c.4992C>T (p.Leu1664=)	rs142459158	0.00061
NM_007294.4(BRCA1):c.1487G>A (p.Arg496His)	rs28897677	0.00060
NM_007294.4(BRCA1):c.5348T>C (p.Met1783Thr)	rs55808233	0.00058
NM_007294.4(BRCA1):c.2566T>C (p.Tyr856His)	rs80356892	0.00046
NM_007294.4(BRCA1):c.1648A>C (p.Asn550His)	rs56012641	0.00029
NM_007294.4(BRCA1):c.536A>G (p.Tyr179Cys)	rs56187033	0.00029
NM_007294.4(BRCA1):c.736T>G (p.Leu246Val)	rs28897675	0.00026
NM_007294.4(BRCA1):c.1486C>T (p.Arg496Cys)	rs28897676	0.00023
NM_007294.4(BRCA1):c.2477C>A (p.Thr826Lys)	rs28897683	0.00021
NM_007294.4(BRCA1):c.4484+14A>G	rs80358022	0.00019
NM_007294.4(BRCA1):c.1065G>A (p.Lys355=)	rs41286292	0.00011
NM_007294.4(BRCA1):c.4358-2725T>C	rs374519494	0.00011
NM_007294.4(BRCA1):c.693G>A (p.Thr231=)	rs62625298	0.00011
NM_007294.4(BRCA1):c.4882A>G (p.Met1628Val)	rs80357465	0.00008
NM_007294.4(BRCA1):c.75C>T (p.Pro25=)	rs80356839	0.00004
NM_007294.4(BRCA1):c.396C>A (p.Asn132Lys)	rs80357413	0.00003
NM_007294.4(BRCA1):c.5153-6C>A	rs80358129	0.00002
NM_007294.4(BRCA1):c.1401G>A (p.Lys467=)	rs786201323	0.00001
NM_007294.4(BRCA1):c.4204C>T (p.His1402Tyr)	rs80357365	0.00001
NM_007294.4(BRCA1):c.996G>T (p.Arg332=)	rs80356836	0.00001
NM_007294.4(BRCA1):c.1843TCT[1] (p.Ser616del)	rs80358329
NM_007294.4(BRCA1):c.81-14C>G	rs80358006

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