Overview

This tab shows an overview (JBrowse graphic) for the non-coding variant (NCV) [more details]
Mutation ID ( COSV )
101017038
Legacy Mutation ID ( COSN )
COSN30102286
FATHMM-MKL Score
0.2796 (not functionally significant)
Genomic Summary

Details

This tab shows the deatils for the non-coding variant (NCV) [more details]
Mutation ID (COSV)
101017038
Syntax
13:g.30208452A>C
Type
Substitution
Sample/Tissue
TCGA-19-5956-01 / Central nervous system
References
Studies
329
Genome Location
13:30208452..30208452
Browser Links