Overview

This tab shows an overview (JBrowse graphic) for the non-coding variant (NCV) [more details]
Mutation ID ( COSV )
104400092
Legacy Mutation ID ( COSN )
COSN31793028
FATHMM-MKL Score
0.0000 (not functionally significant)
Genomic Summary

Details

This tab shows the deatils for the non-coding variant (NCV) [more details]
Mutation ID (COSV)
104400092
Syntax
2:g.60923055_60923056del
Type
Deletion
Sample/Tissue
MEN0121-P4 / Meninges
References
28713588
Studies
Genome Location
2:60923055..60923056
Browser Links