Overview

This tab shows an overview (JBrowse graphic) for the non-coding variant (NCV) [more details]
Mutation ID ( COSV )
100041569
Legacy Mutation ID ( COSN )
COSN30457909
FATHMM-MKL Score
0.2673 (not functionally significant)
Genomic Summary

Details

This tab shows the deatils for the non-coding variant (NCV) [more details]
Mutation ID (COSV)
100041569
Syntax
6:g.27223109C>T
Type
Substitution
Sample/Tissue
TCGA-BF-AAOX-01 / Skin
References
Studies
540
Genome Location
6:27223109..27223109
Browser Links