Overview

This tab shows an overview (JBrowse graphic) for the non-coding variant (NCV) [more details]
Mutation ID ( COSV )
99388653
Legacy Mutation ID ( COSN )
COSN30498150
FATHMM-MKL Score
0.9444 (functionally significant)
Genomic Summary

Details

This tab shows the deatils for the non-coding variant (NCV) [more details]
Mutation ID (COSV)
99388653
Syntax
19:g.29823813C>T
Type
Substitution
Sample/Tissue
TCGA-BR-8487-01 / Stomach
References
Studies
541
Genome Location
19:29823813..29823813
Browser Links