List of variants in gene BRCA1 reported as uncertain significance by Foulkes Cancer Genetics LDI, Lady Davis Institute for Medical Research

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_007294.4(BRCA1):c.5348T>C (p.Met1783Thr)	rs55808233	0.00058
NM_007294.4(BRCA1):c.2368A>G (p.Thr790Ala)	rs41286298	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.4132G>A (p.Val1378Ile)	rs28897690	0.00017
NM_007294.4(BRCA1):c.994C>T (p.Arg332Trp)	rs80357176	0.00002
NM_007294.4(BRCA1):c.212+3A>G	rs80358083	0.00001
NM_007294.4(BRCA1):c.3092T>G (p.Ile1031Ser)	rs863224758	0.00001
NM_007294.4(BRCA1):c.4816A>G (p.Lys1606Glu)	rs80356943	0.00001
NM_007294.4(BRCA1):c.5096G>A (p.Arg1699Gln)	rs41293459	0.00001
NM_007294.4(BRCA1):c.2392C>G (p.Pro798Ala)	rs398122658
NM_007294.4(BRCA1):c.5090G>A (p.Cys1697Tyr)	rs397507241
NM_007294.4(BRCA1):c.5216A>G (p.Asp1739Gly)	rs80357227
NM_007294.4(BRCA1):c.5236C>T (p.His1746Tyr)	rs80357146
NM_007294.4(BRCA1):c.74C>T (p.Pro25Leu)	rs876660096
NM_007294.4(BRCA1):c.754C>T (p.Arg252Cys)	rs273902786
NM_007294.4(BRCA1):c.97G>C (p.Glu33Gln)	rs80357066

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