Overview

This tab shows an overview (JBrowse graphic) for the non-coding variant (NCV) [more details]
Mutation ID ( COSV )
105033494
Legacy Mutation ID ( COSN )
COSN32071702
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)
105033494
Syntax
17:g.81868793_81868794delinsGG
Type
Complex - compound substitution
Sample/Tissue
DD107_PT / Stomach
References
29703791
Studies
Genome Location
17:81868793..81868794
Browser Links