List of variants in gene BRCA1 reported as benign by Mendelics

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: 47

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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.3119G>A (p.Ser1040Asn)	rs4986852	0.01109
NM_007294.4(BRCA1):c.557C>A (p.Ser186Tyr)	rs55688530	0.00301
NM_007294.4(BRCA1):c.2167A>G (p.Asn723Asp)	rs4986845	0.00209
NM_007294.4(BRCA1):c.4682C>T (p.Thr1561Ile)	rs56158747	0.00150
NM_007294.4(BRCA1):c.4883T>C (p.Met1628Thr)	rs4986854	0.00098
NM_007294.4(BRCA1):c.3022A>G (p.Met1008Val)	rs56321129	0.00095
NM_007294.4(BRCA1):c.4691T>C (p.Leu1564Pro)	rs56119278	0.00059
NM_007294.4(BRCA1):c.4675+55A>G	rs934064952	0.00040
NM_007294.4(BRCA1):c.1036C>T (p.Pro346Ser)	rs80357015	0.00032
NM_007294.4(BRCA1):c.736T>G (p.Leu246Val)	rs28897675	0.00026
NM_007294.4(BRCA1):c.4484+14A>G	rs80358022	0.00019
NM_007294.4(BRCA1):c.5406+33A>T	rs80358092	0.00018
NM_007294.4(BRCA1):c.2315T>C (p.Val772Ala)	rs80357467	0.00012
NM_007294.4(BRCA1):c.4934G>C (p.Arg1645Thr)	rs70953661	0.00011
NM_007294.4(BRCA1):c.4882A>G (p.Met1628Val)	rs80357465	0.00008
NM_007294.4(BRCA1):c.1865C>T (p.Ala622Val)	rs56039126	0.00007
NM_007294.4(BRCA1):c.1392C>T (p.Thr464=)	rs533802049	0.00006
NM_007294.4(BRCA1):c.301+55G>A	rs868735744	0.00005
NM_007294.4(BRCA1):c.1511G>A (p.Arg504His)	rs56272539	0.00004
NM_007294.4(BRCA1):c.2286A>T (p.Arg762Ser)	rs273898682	0.00004
NM_007294.4(BRCA1):c.4261C>T (p.His1421Tyr)	rs80357013	0.00004
NM_007294.4(BRCA1):c.5252G>A (p.Arg1751Gln)	rs80357442	0.00004
NM_007294.4(BRCA1):c.811G>A (p.Val271Met)	rs80357244	0.00003
NM_007294.4(BRCA1):c.2006T>C (p.Met669Thr)	rs80356895	0.00002
NM_007294.4(BRCA1):c.5531T>G (p.Leu1844Arg)	rs80357323	0.00002
NM_007294.4(BRCA1):c.824G>A (p.Gly275Asp)	rs397509327	0.00002
NM_007294.4(BRCA1):c.1258G>T (p.Asp420Tyr)	rs80357488	0.00001
NM_007294.4(BRCA1):c.1401G>A (p.Lys467=)	rs786201323	0.00001
NM_007294.4(BRCA1):c.1797T>C (p.Asn599=)	rs756211343	0.00001
NM_007294.4(BRCA1):c.2468G>T (p.Arg823Ile)	rs876659731	0.00001
NM_007294.4(BRCA1):c.2597G>A (p.Arg866His)	rs80356911	0.00001
NM_007294.4(BRCA1):c.4166G>A (p.Ser1389Asn)	rs78951648	0.00001
NM_007294.4(BRCA1):c.4816A>G (p.Lys1606Glu)	rs80356943	0.00001
NM_007294.4(BRCA1):c.4910C>T (p.Pro1637Leu)	rs80357048	0.00001
NM_007294.4(BRCA1):c.5573T>C (p.Ile1858Thr)	rs755427809	0.00001
NM_007294.4(BRCA1):c.1106_1108del (p.Asp369del)	rs80358325
NM_007294.4(BRCA1):c.1912G>A (p.Glu638Lys)	rs80357005
NM_007294.4(BRCA1):c.2612C>T (p.Pro871Leu)	rs799917
NM_007294.4(BRCA1):c.2798G>C (p.Gly933Ala)	rs80356941
NM_007294.4(BRCA1):c.441+36_441+49del	rs373413425
NM_007294.4(BRCA1):c.5095C>A (p.Arg1699=)	rs55770810
NM_007294.4(BRCA1):c.5152+80del	rs902919427
NM_007294.4(BRCA1):c.577A>G (p.Lys193Glu)	rs878854962
NM_007294.4(BRCA1):c.652T>G (p.Leu218Val)	rs765950064
NM_007294.4(BRCA1):c.81-14C>T	rs80358006
NM_007294.4(BRCA1):c.823G>A (p.Gly275Ser)	rs8176153

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