BRCA1 c.5387dup ;(p.S1797Ifs*33)

Variant ID: 17-41201156-T-TG

NM_007294.3(BRCA1):c.5387dup;(p.S1797Ifs*33)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


High likelihood of actionable pathogenic variant detection in breast cancer genes in women with very early onset breast cancer.

Journal Of Medical Genetics
Evans, D Gareth DG; van Veen, Elke Maria EM; Byers, Helen J HJ; Evans, Sarah J SJ; Burghel, George J GJ; Woodward, Emma Roisin ER; Harkness, Elaine F EF; Eccles, Diana M DM; Greville-Haygate, Stephanie L SL; Ellingford, Jamie M JM; Bowers, Naomi L NL; Pereira, Marta M; Wallace, Andrew J AJ; Howell, Sasha J SJ; Howell, Anthony A; Lalloo, Fiona F; Newman, William G WG; Smith, Miriam Jane MJ
Publication Date: 2022-02

Variant appearance in text: BRCA1: 5387dupC; Ser1797Ilefs*33
PubMed Link: 33758026
Variant Present in the following documents:
  • jmedgenet-2020-107347supp001.pdf
View BVdb publication page



High likelihood of actionable pathogenic variant detection in breast cancer genes in women with very early onset breast cancer.

Journal Of Medical Genetics
Evans, D Gareth DG; van Veen, Elke Maria EM; Byers, Helen J HJ; Evans, Sarah J SJ; Burghel, George J GJ; Woodward, Emma Roisin ER; Harkness, Elaine F EF; Eccles, Diana M DM; Greville-Haygate, Stephanie L SL; Ellingford, Jamie M JM; Bowers, Naomi L NL; Pereira, Marta M; Wallace, Andrew J AJ; Howell, Sasha J SJ; Howell, Anthony A; Lalloo, Fiona F; Newman, William G WG; Smith, Miriam Jane MJ
Publication Date: 2021-03-23

Variant appearance in text: BRCA1: 5387dupC; Ser1797Ilefs*33
PubMed Link: 33758026
Variant Present in the following documents:
  • jmedgenet-2020-107347supp001.pdf
View BVdb publication page