Overview

This tab shows an overview (JBrowse graphic) for the non-coding variant (NCV) [more details]
Mutation ID ( COSV )
52766188
Legacy Mutation ID ( COSN )
COSN26957284
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)
52766188
Syntax
9:g.92032456_92032457delinsAA
Type
Complex - compound substitution
Sample/Tissue
MCC_274 / Skin
References
26238782
Studies
Genome Location
9:92032456..92032457
Browser Links