Overview

This tab shows an overview (JBrowse graphic) for the non-coding variant (NCV) [more details]
Mutation ID ( COSV )
105088699
Legacy Mutation ID ( COSN )
COSN32064889
FATHMM-MKL Score
0.6284 (not functionally significant)
Genomic Summary

Details

This tab shows the deatils for the non-coding variant (NCV) [more details]
Mutation ID (COSV)
105088699
Syntax
14:g.39182662G>C
Type
Substitution
Sample/Tissue
ESCC_00522 / Oesophagus
References
27058444
Studies
Genome Location
14:39182662..39182662
Browser Links