Overview

This tab shows an overview (JBrowse graphic) for the non-coding variant (NCV) [more details]
Mutation ID ( COSV )
100022598
Legacy Mutation ID ( COSN )
COSN30169317
FATHMM-MKL Score
0.1968 (not functionally significant)
Genomic Summary

Details

This tab shows the deatils for the non-coding variant (NCV) [more details]
Mutation ID (COSV)
100022598
Syntax
17:g.759994G>C
Type
Substitution
Sample/Tissue
TCGA-E9-A1R4-01 / Breast
References
Studies
414
Genome Location
17:759994..759994
Browser Links