Overview

This tab shows an overview (JBrowse graphic) for the non-coding variant (NCV) [more details]
Mutation ID ( COSV )
105214599
Legacy Mutation ID ( COSN )
COSN32065788
FATHMM-MKL Score
0.7678 (functionally significant)
Genomic Summary

Details

This tab shows the deatils for the non-coding variant (NCV) [more details]
Mutation ID (COSV)
105214599
Syntax
2:g.178431899G>A
Type
Substitution
Sample/Tissue
ESCC_00221 / Oesophagus
References
27058444
Studies
Genome Location
2:178431899..178431899
Browser Links