PARP2 c.464A>G ;(p.N155S)

Variant ID: 14-20819248-A-G

NM_001042618.1(PARP2):c.464A>G;(p.N155S)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


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: rs3093906
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: rs3093906
PubMed Link: 18518984
Variant Present in the following documents:
  • Main text
  • 1471-2164-9-265.pdf
View BVdb publication page