Overview

This tab shows an overview (JBrowse graphic) for the non-coding variant (NCV) [more details]
Mutation ID ( COSV )
100327178
Legacy Mutation ID ( COSN )
COSN30134614
FATHMM-MKL Score
0.9399 (functionally significant)
Genomic Summary

Details

This tab shows the deatils for the non-coding variant (NCV) [more details]
Mutation ID (COSV)
100327178
Syntax
3:g.181713809A>G
Type
Substitution
Sample/Tissue
TCGA-AA-3984-01 / Large intestine
References
Studies
376
Genome Location
3:181713809..181713809
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