Overview

This tab shows an overview (JBrowse graphic) for the non-coding variant (NCV) [more details]
Mutation ID ( COSV )
104997069
Legacy Mutation ID ( COSN )
COSN32057802
FATHMM-MKL Score
0.0973 (not functionally significant)
Genomic Summary

Details

This tab shows the deatils for the non-coding variant (NCV) [more details]
Mutation ID (COSV)
104997069
Syntax
7:g.156971153A>G
Type
Substitution
Sample/Tissue
CRC_47 / Large intestine
References
30239619
Studies
Genome Location
7:156971153..156971153
Browser Links