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FIGN c.1057G>T ;(p.D353Y)
Variant ID: 2-164467285-C-A
NM_018086.2(
FIGN
):c.1057G>T;(p.D353Y)
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: 1057G>T; D353Y
PubMed Link:
30602096
Variant Present in the following documents:
Main text
gi-2018-16-4-e35.pdf
View BVdb publication page