Overview

This tab shows an overview (JBrowse graphic) for the non-coding variant (NCV) [more details]
Mutation ID ( COSV )
53906339
Legacy Mutation ID ( COSN )
COSN26859644
FATHMM-MKL Score
0.2946 (not functionally significant)
Genomic Summary

Details

This tab shows the deatils for the non-coding variant (NCV) [more details]
Mutation ID (COSV)
53906339
Syntax
17:g.81868419C>T
Type
Substitution
Sample/Tissue
W18T / Thyroid
References
Studies
676
Genome Location
17:81868419..81868419
Browser Links