Overview

This tab shows an overview (JBrowse graphic) for the non-coding variant (NCV) [more details]
Mutation ID ( COSV )
99330774
Legacy Mutation ID ( COSN )
COSN30494176
FATHMM-MKL Score
0.2062 (not functionally significant)
Genomic Summary

Details

This tab shows the deatils for the non-coding variant (NCV) [more details]
Mutation ID (COSV)
99330774
Syntax
22:g.35393652T>C
Type
Substitution
Sample/Tissue
TCGA-HU-A4GH-01 / Stomach
References
Studies
541
Genome Location
22:35393652..35393652
Browser Links