PARP2 c.814A>G ;(p.I272V)

Variant ID: 14-20823018-A-G

NM_001042618.1(PARP2):c.814A>G;(p.I272V)

This variant was identified in 3 publications

View GRCh38 version.




Publications:


Discovery of actionable genetic alterations with targeted panel sequencing in children with relapsed or refractory solid tumors.

Plos One
Lee, Ji Won JW; Kim, Nayoung K D NKD; Lee, Soo Hyun SH; Cho, Hee Won HW; Ma, Youngeun Y; Ju, Hee Young HY; Yoo, Keon Hee KH; Sung, Ki Woong KW; Koo, Hong Hoe HH; Park, Woong-Yang WY
Publication Date: 2019

Variant appearance in text: rs3093925
PubMed Link: 31747416
Variant Present in the following documents:
  • pone.0224227.s002.xlsx, sheet 1
View BVdb publication page



Reproducible Analysis of Post-Translational Modifications in Proteomes--Application to Human Mutations.

Plos One
Holehouse, Alex S AS; Naegle, Kristen M KM
Publication Date: 2015

Variant appearance in text: rs3093925
PubMed Link: 26659599
Variant Present in the following documents:
  • pone.0144692.s002.xlsx, sheet 1
View BVdb publication page



Genome-wide survey of allele-specific splicing in humans.

Bmc Genomics
Nembaware, Victoria V; Lupindo, Bukiwe B; Schouest, Katherine K; Spillane, Charles C; Scheffler, Konrad K; Seoighe, Cathal C
Publication Date: 2008-06-02

Variant appearance in text: rs3093925
PubMed Link: 18518984
Variant Present in the following documents:
  • Main text
  • 1471-2164-9-265.pdf
View BVdb publication page