FIGN c.2104G>C ;(p.V702L)

Variant ID: 2-164466238-C-G

NM_018086.2(FIGN):c.2104G>C;(p.V702L)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

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: FIGN: 2104G>C; V702L
PubMed Link: 30602096
Variant Present in the following documents:
  • Main text
  • gi-2018-16-4-e35.pdf
View BVdb publication page