Overview

This tab shows an overview (JBrowse graphic) for the non-coding variant (NCV) [more details]
Mutation ID ( COSV )
52365237
Legacy Mutation ID ( COSN )
COSN23987494
FATHMM-MKL Score
0.3082 (not functionally significant)
Genomic Summary

Details

This tab shows the deatils for the non-coding variant (NCV) [more details]
Mutation ID (COSV)
52365237
Syntax
2:g.224471218G>C
Type
Substitution
Sample/Tissue
PTC_328 / Thyroid
References
Studies
589
Genome Location
2:224471218..224471218
Browser Links