ATM c.2503_2507del ;(p.V835Ifs*5)

Variant ID: 11-108137932-AAGTAG-A

NM_000051.3(ATM):c.2503_2507del;(p.V835Ifs*5)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Reanalysis of BRCA1/2 negative high risk ovarian cancer patients reveals novel germline risk loci and insights into missing heritability.

Plos One
Stafford, Jaime L JL; Dyson, Gregory G; Levin, Nancy K NK; Chaudhry, Sophia S; Rosati, Rita R; Kalpage, Hasini H; Wernette, Courtney C; Petrucelli, Nancie N; Simon, Michael S MS; Tainsky, Michael A MA
Publication Date: 2017

Variant appearance in text: ATM: 2503_2507del
PubMed Link: 28591191
Variant Present in the following documents:
  • Main text
  • pone.0178450.pdf
View BVdb publication page



Use of Whole Genome Sequencing for Diagnosis and Discovery in the Cancer Genetics Clinic.

Ebiomedicine
Foley, Samantha B SB; Rios, Jonathan J JJ; Mgbemena, Victoria E VE; Robinson, Linda S LS; Hampel, Heather L HL; Toland, Amanda E AE; Durham, Leslie L; Ross, Theodora S TS
Publication Date: 2015-01

Variant appearance in text: N/A
PubMed Link: 26023681
Variant Present in the following documents:
View BVdb publication page