Overview

This tab shows an overview (JBrowse graphic) for the non-coding variant (NCV) [more details]
Mutation ID ( COSV )
57131545
Legacy Mutation ID ( COSN )
COSN8992555
FATHMM-MKL Score
0.7392 (functionally significant)
Genomic Summary

Details

This tab shows the deatils for the non-coding variant (NCV) [more details]
Mutation ID (COSV)
57131545
Syntax
19:g.12943967G>T
Type
Substitution
Sample/Tissue
PTC-28C / Thyroid
References
Studies
589
Genome Location
19:12943967..12943967
Browser Links