PTPN22 c.796C>A ;(p.R266=)

Variant ID: 1-114394681-G-T

NM_015967.5(PTPN22):c.796C>A;(p.R266=)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


BaalChIP: Bayesian analysis of allele-specific transcription factor binding in cancer genomes.

Genome Biology
de Santiago, Ines I; Liu, Wei W; Yuan, Ke K; O'Reilly, Martin M; Chilamakuri, Chandra Sekhar Reddy CS; Ponder, Bruce A J BA; Meyer, Kerstin B KB; Markowetz, Florian F
Publication Date: 2017-02-24

Variant appearance in text: rs72650670
PubMed Link: 28235418
Variant Present in the following documents:
  • Main text
  • 13059_2017_Article_1165.pdf
View BVdb publication page