Cosmic » Non-Coding Variant » Overview » 99777048

Overview

This tab shows an overview (JBrowse graphic) for the non-coding variant (NCV) [more details]
Mutation ID ( COSV )
99777048
Legacy Mutation ID ( COSN )
COSN30509580
FATHMM-MKL Score
0.9530 (functionally significant)
Genomic Summary

Details

This tab shows the deatils for the non-coding variant (NCV) [more details]
Mutation ID (COSV)
99777048
Syntax
4:g.44705021T>A
Type
Substitution
Sample/Tissue
TCGA-EM-A1YB-01 / Thyroid
References
Studies
542
Genome Location
4:44705021..44705021
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