APC c.937G>C ;(p.E313Q)

Variant ID: 5-112154666-G-C

NM_000038.5(APC):c.937G>C;(p.E313Q)

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:

Mutation of the H-helix in antithrombin decreases heparin stimulation of protease inhibition.

Biochimica Et Biophysica Acta
Gonzales, Patrick R PR; Walston, Timothy D TD; Camacho, Laureano O LO; Kielar, Dana M DM; Church, Frank C FC; Rezaie, Alireza R AR; Cooper, Scott T ST
Publication Date: 2007-11

Variant appearance in text: APC: E313Q
PubMed Link: 17905675
Variant Present in the following documents:
  • Main text
View BVdb publication page