STN1 c.41C>A ;(p.S14Y)

Variant ID: 10-105677312-G-T

NM_024928.4(STN1):c.41C>A;(p.S14Y)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Comparative sequencing analysis reveals high genomic concordance between matched primary and metastatic colorectal cancer lesions.

Genome Biology
Brannon, A Rose AR; Vakiani, Efsevia E; Sylvester, Brooke E BE; Scott, Sasinya N SN; McDermott, Gregory G; Shah, Ronak H RH; Kania, Krishan K; Viale, Agnes A; Oschwald, Dayna M DM; Vacic, Vladimir V; Emde, Anne-Katrin AK; Cercek, Andrea A; Yaeger, Rona R; Kemeny, Nancy E NE; Saltz, Leonard B LB; Shia, Jinru J; D'Angelica, Michael I MI; Weiser, Martin R MR; Solit, David B DB; Berger, Michael F MF
Publication Date: 2014-08-28

Variant appearance in text: OBFC1: 41C>A
PubMed Link: 25164765
Variant Present in the following documents:
  • 13059_2014_454_MOESM5_ESM.xlsx, sheet 1
View BVdb publication page