Overview

This tab shows an overview (JBrowse graphic) for the non-coding variant (NCV) [more details]
Mutation ID ( COSV )
104401771
Legacy Mutation ID ( COSN )
COSN31813296
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)
104401771
Syntax
3:g.196557772_196557773insATTTT
Type
Insertion
Sample/Tissue
MEN0054G-P / Meninges
References
28713588
Studies
Genome Location
3:196557772..196557773
Browser Links