Overview

This tab shows an overview (JBrowse graphic) for the non-coding variant (NCV) [more details]
Mutation ID ( COSV )
62686767
Legacy Mutation ID ( COSN )
COSN26856878
FATHMM-MKL Score
0.9695 (functionally significant)
Genomic Summary

Details

This tab shows the deatils for the non-coding variant (NCV) [more details]
Mutation ID (COSV)
62686767
Syntax
6:g.26376827G>A
Type
Substitution
Sample/Tissue
W5T / Thyroid
References
Studies
676
Genome Location
6:26376827..26376827
Browser Links