Cosmic » Non-Coding Variant » Overview » 100265829

Overview

This tab shows an overview (JBrowse graphic) for the non-coding variant (NCV) [more details]
Mutation ID ( COSV )
100265829
Legacy Mutation ID ( COSN )
COSN30122169
FATHMM-MKL Score
0.9183 (functionally significant)
Genomic Summary

Details

This tab shows the deatils for the non-coding variant (NCV) [more details]
Mutation ID (COSV)
100265829
Syntax
19:g.37738440C>T
Type
Substitution
Sample/Tissue
TCGA-DM-A0XF-01 / Large intestine
References
Studies
376
Genome Location
19:37738440..37738440
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