PICALM c.1361A>G ;(p.D454G)

Variant ID: 11-85701340-T-C

NM_007166.3(PICALM):c.1361A>G;(p.D454G)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Sequencing for germline mutations in Swedish breast cancer families reveals novel breast cancer risk genes.

Scientific Reports
Helgadottir, Hafdis T HT; Thutkawkorapin, Jessada J; Lagerstedt-Robinson, Kristina K; Lindblom, Annika A
Publication Date: 2021-07-19

Variant appearance in text: rs184756078
PubMed Link: 34282249
Variant Present in the following documents:
  • 41598_2021_94316_MOESM1_ESM.xlsx, sheet 2
View BVdb publication page