Overview

This tab shows an overview (JBrowse graphic) for the non-coding variant (NCV) [more details]
Mutation ID ( COSV )
100744568
Legacy Mutation ID ( COSN )
COSN30124801
FATHMM-MKL Score
0.0969 (not functionally significant)
Genomic Summary

Details

This tab shows the deatils for the non-coding variant (NCV) [more details]
Mutation ID (COSV)
100744568
Syntax
19:g.52065043T>A
Type
Substitution
Sample/Tissue
TCGA-AA-A022-01 / Large intestine
References
Studies
376
Genome Location
19:52065043..52065043
Browser Links