Overview

This tab shows an overview (JBrowse graphic) for the non-coding variant (NCV) [more details]
Mutation ID ( COSV )
104386391
Legacy Mutation ID ( COSN )
COSN31849346
FATHMM-MKL Score
0.2181 (not functionally significant)
Genomic Summary

Details

This tab shows the deatils for the non-coding variant (NCV) [more details]
Mutation ID (COSV)
104386391
Syntax
7:g.33014689A>T
Type
Substitution
Sample/Tissue
MEN0093-P1 / Meninges
References
28713588
Studies
Genome Location
7:33014689..33014689
Browser Links