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Table 5 BRCA1 and BRCA2 variants of unknown significance detected in families with breast and ovarian cancer

From: Molecular analysis of BRCA1 and BRCA2 genes in La Rioja (Spain): five new variants

Gene

Exon

HGVS nomenclature

HGVS protein

ACMG classification

gnomAD exomes

gnomAD genomes

BRCA1

11

c.1661 A > G

p.Glu554Gly

Likely benign

No data

No data

 

11

c.3047 A > G

p.Asn1016Ser

Likely benign

No data

No data

 

11

c.4046 C > G

p.Thr1349Arg

Likely benign

No data

No data

 

17

c.5017_5019delCAC

p.His1673delHis

Uncertain significance

No data

No data

BRCA2

      
 

7

c.632–3 C > G

(intron 7)

Pathologic

0.00000411

No data

  

c.68-7del

 

Uncertain significance

No data

No data

 

7

c.565G > T

p.Asp189Tyr

Uncertain significance

No data

No data

 

10

c.1096T > G

p.Leu366Val

Likely benign

0.0000281

No data

 

11

c.3170 A > G

p.Lys1057Arg

Uncertain significance

No data

No data

 

11

c.3299 A > T

p.Asn1100Ile

Uncertain significance

0.0000131

No data

 

11

c.3794G > A

p.Cys1265Tyr

Likely benign

No data

No data

 

11

c.5729 A > T

p.Asn1910Ile

Likely benign

No data

0.0000318

 

26

c.9530 A > G

p.Glu3177Gly

Uncertain significance

0.00000796

No data