Overview

This tab shows an overview (JBrowse graphic) for the non-coding variant (NCV) [more details]
Mutation ID ( COSV )
53210700
Legacy Mutation ID ( COSN )
COSN23987328
FATHMM-MKL Score
0.9518 (functionally significant)
Genomic Summary

Details

This tab shows the deatils for the non-coding variant (NCV) [more details]
Mutation ID (COSV)
53210700
Syntax
19:g.17603125G>T
Type
Substitution
Sample/Tissue
PTC_514 / Thyroid
References
Studies
589
Genome Location
19:17603125..17603125
Browser Links