Overview

This tab shows an overview (JBrowse graphic) for the non-coding variant (NCV) [more details]
Mutation ID ( COSV )
99509822
Legacy Mutation ID ( COSN )
COSN30479499
FATHMM-MKL Score
0.9023 (functionally significant)
Genomic Summary

Details

This tab shows the deatils for the non-coding variant (NCV) [more details]
Mutation ID (COSV)
99509822
Syntax
17:g.38974646G>T
Type
Substitution
Sample/Tissue
TCGA-EE-A2MM-06 / Skin
References
Studies
540
Genome Location
17:38974646..38974646
Browser Links