Variants with conflicting interpretations "benign" from National Health Laboratory Service, Universitas Academic Hospital and University of the Free State and "likely benign" from any submitter

Minimum review status of the submission from National Health Laboratory Service, Universitas Academic Hospital and University of the Free State:		Collection method of the submission from National Health Laboratory Service, Universitas Academic Hospital and University of the Free State:
Minimum review status of the other submission:		Collection method of the other submission:
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 41

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HGVS	dbSNP	gnomAD frequency
NM_007294.4(BRCA1):c.3119G>A (p.Ser1040Asn)	rs4986852	0.01109
NM_000059.4(BRCA2):c.8487+19A>G	rs11571743	0.01055
NM_007294.4(BRCA1):c.3418A>G (p.Ser1140Gly)	rs2227945	0.01054
NM_007294.4(BRCA1):c.212+23T>A	rs8176128	0.01018
NM_000059.4(BRCA2):c.7319A>G (p.His2440Arg)	rs4986860	0.00984
NM_007294.4(BRCA1):c.2458A>G (p.Lys820Glu)	rs56082113	0.00964
NM_000059.4(BRCA2):c.3264T>C (p.Pro1088=)	rs36060526	0.00793
NM_000059.4(BRCA2):c.7017G>C (p.Lys2339Asn)	rs45574331	0.00792
NM_000059.4(BRCA2):c.9730G>A (p.Val3244Ile)	rs11571831	0.00792
NM_007294.4(BRCA1):c.4039A>G (p.Arg1347Gly)	rs28897689	0.00419
NM_000059.4(BRCA2):c.1275A>G (p.Glu425=)	rs34355306	0.00335
NM_000059.4(BRCA2):c.3869G>A (p.Cys1290Tyr)	rs41293485	0.00307
NM_007294.4(BRCA1):c.557C>A (p.Ser186Tyr)	rs55688530	0.00301
NM_000059.4(BRCA2):c.4068G>A (p.Leu1356=)	rs28897724	0.00295
NM_000059.4(BRCA2):c.4681C>A (p.His1561Asn)	rs2219594	0.00292
NM_000059.4(BRCA2):c.7805+6C>G	rs81002819	0.00290
NM_000059.4(BRCA2):c.6100C>T (p.Arg2034Cys)	rs1799954	0.00268
NM_000059.4(BRCA2):c.6220C>A (p.His2074Asn)	rs34309943	0.00264
NM_007294.4(BRCA1):c.4535G>T (p.Ser1512Ile)	rs1800744	0.00240
NM_000059.4(BRCA2):c.7150C>A (p.Gln2384Lys)	rs55977008	0.00203
NM_000059.4(BRCA2):c.231T>G (p.Thr77=)	rs114446594	0.00191
NM_007294.4(BRCA1):c.2814A>G (p.Pro938=)	rs80356851	0.00183
NM_007294.4(BRCA1):c.21C>T (p.Arg7=)	rs149402012	0.00165
NM_000059.4(BRCA2):c.125A>G (p.Tyr42Cys)	rs4987046	0.00158
NM_007294.4(BRCA1):c.4682C>T (p.Thr1561Ile)	rs56158747	0.00150
NM_007294.4(BRCA1):c.4600G>A (p.Val1534Met)	rs55815649	0.00145
NM_000059.4(BRCA2):c.9235G>A (p.Val3079Ile)	rs55933907	0.00106
NM_007294.4(BRCA1):c.3024G>A (p.Met1008Ile)	rs1800704	0.00065
NM_007294.4(BRCA1):c.301+8T>C	rs80358101	0.00054
NM_000059.4(BRCA2):c.317-22C>T	rs81002794	0.00024
NM_000059.4(BRCA2):c.467A>G (p.Asp156Gly)	rs68071147	0.00022
NM_000059.4(BRCA2):c.5312G>A (p.Gly1771Asp)	rs80358755	0.00021
NM_000059.4(BRCA2):c.1123C>T (p.Pro375Ser)	rs80358408	0.00019
NM_000059.4(BRCA2):c.517-4C>G	rs81002804	0.00008
NM_007294.4(BRCA1):c.593+3G>A	rs80358013	0.00007
NM_007294.4(BRCA1):c.4046C>T (p.Thr1349Met)	rs80357345	0.00005
NM_007294.4(BRCA1):c.2669G>T (p.Gly890Val)	rs80356874	0.00004
NM_000059.4(BRCA2):c.927A>G (p.Ser309=)	rs80359806	0.00001
NM_000059.4(BRCA2):c.987G>A (p.Arg329=)	rs561002197	0.00001
NM_000059.4(BRCA2):c.4143AGA[1] (p.Glu1382del)	rs80359432
NM_007294.4(BRCA1):c.663A>G (p.Ala221=)	rs375952040

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