Overview

This tab shows an overview (JBrowse graphic) for the non-coding variant (NCV) [more details]
Mutation ID ( COSV )
100041661
Legacy Mutation ID ( COSN )
COSN30495776
FATHMM-MKL Score
0.1865 (not functionally significant)
Genomic Summary

Details

This tab shows the deatils for the non-coding variant (NCV) [more details]
Mutation ID (COSV)
100041661
Syntax
6:g.27255326C>T
Type
Substitution
Sample/Tissue
TCGA-BR-8368-01 / Stomach
References
Studies
541
Genome Location
6:27255326..27255326
Browser Links