NCAN c.1642G>T ;(p.V548L)

Variant ID: 19-19337864-G-T

NM_004386.2(NCAN):c.1642G>T;(p.V548L)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


The impact of tumor profiling approaches and genomic data strategies for cancer precision medicine.

Genome Medicine
Garofalo, Andrea A; Sholl, Lynette L; Reardon, Brendan B; Taylor-Weiner, Amaro A; Amin-Mansour, Ali A; Miao, Diana D; Liu, David D; Oliver, Nelly N; MacConaill, Laura L; Ducar, Matthew M; Rojas-Rudilla, Vanesa V; Giannakis, Marios M; Ghazani, Arezou A; Gray, Stacy S; Janne, Pasi P; Garber, Judy J; Joffe, Steve S; Lindeman, Neal N; Wagle, Nikhil N; Garraway, Levi A LA; Van Allen, Eliezer M EM
Publication Date: 2016-07-26

Variant appearance in text: NCAN: 1642G>T; V548L; rs150701551
PubMed Link: 27460824
Variant Present in the following documents:
  • 13073_2016_333_MOESM5_ESM.xlsx, sheet 1
View BVdb publication page



Exome-wide association study identifies a TM6SF2 variant that confers susceptibility to nonalcoholic fatty liver disease.

Nature Genetics
Kozlitina, Julia J; Smagris, Eriks E; Stender, Stefan S; Nordestgaard, Børge G BG; Zhou, Heather H HH; Tybjærg-Hansen, Anne A; Vogt, Thomas F TF; Hobbs, Helen H HH; Cohen, Jonathan C JC
Publication Date: 2014-04

Variant appearance in text: NCAN: V548L; rs150701551
PubMed Link: 24531328
Variant Present in the following documents:
  • NIHMS560851-supplement-1.pdf
View BVdb publication page