PCNA c.415A>G ;(p.M139V)

Variant ID: 20-5098283-T-C

NM_182649.1(PCNA):c.415A>G;(p.M139V)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Extensive disruption of protein interactions by genetic variants across the allele frequency spectrum in human populations.

Nature Communications
Fragoza, Robert R; Das, Jishnu J; Wierbowski, Shayne D SD; Liang, Jin J; Tran, Tina N TN; Liang, Siqi S; Beltran, Juan F JF; Rivera-Erick, Christen A CA; Ye, Kaixiong K; Wang, Ting-Yi TY; Yao, Li L; Mort, Matthew M; Stenson, Peter D PD; Cooper, David N DN; Wei, Xiaomu X; Keinan, Alon A; Schimenti, John C JC; Clark, Andrew G AG; Yu, Haiyuan H
Publication Date: 2019-09-12

Variant appearance in text: PCNA: 415A>G; M139V; rs376351202
PubMed Link: 31515488
Variant Present in the following documents:
  • 41467_2019_11959_MOESM11_ESM.xlsx, sheet 1
  • 41467_2019_11959_MOESM6_ESM.xlsx, sheet 1
View BVdb publication page



PCNA dependent cellular activities tolerate dramatic perturbations in PCNA client interactions.

Dna Repair
Wilson, Rosemary H C RH; Biasutto, Antonio J AJ; Wang, Lihao L; Fischer, Roman R; Baple, Emma L EL; Crosby, Andrew H AH; Mancini, Erika J EJ; Green, Catherine M CM
Publication Date: 2017-02

Variant appearance in text: PCNA: Met139Val; rs376351202
PubMed Link: 28073635
Variant Present in the following documents:
  • Main text
  • main.pdf
View BVdb publication page