RB1 c.1097T>G ;(p.V366G)

Variant ID: 13-48942710-T-G

NM_000321.2(RB1):c.1097T>G;(p.V366G)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Somatic Mutations from Whole Exome Sequencing Analysis of the Patients with Biliary Tract Cancer.

Genomics & Informatics
Yoon, Kyong-Ah KA; Woo, Sang Myung SM; Kim, Yun-Hee YH; Kong, Sun-Young SY; Han, Sung-Sik SS; Park, Sang-Jae SJ; Lee, Woo Jin WJ
Publication Date: 2018-12

Variant appearance in text: RB1: 1097T>G; V366G
PubMed Link: 30602096
Variant Present in the following documents:
  • Main text
  • gi-2018-16-4-e35.pdf
View BVdb publication page