CCT6B - morinlab/LLMPP GitHub Wiki


bibliography: 'morinlab.bib' csl: 'NLM.csl' link-citations: true

CCT6B

Overview

Due to minimal support in the original primary data and very few mutations reported in subsequent studies, this gene is very unlikely to be relevant in BL.

<<Warn("The variants reported in this gene failed QC")>>

History

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timeline
    title Publication timing
      2012-12-01 : Love : BL

Relevance tier by entity

Entity Tier Description
BL 3 Retired, Failed QC[@loveGeneticLandscapeMutations2012]

Mutation incidence in large patient cohorts (GAMBL reanalysis)

Entity source frequency (%)
BL GAMBL genomes+capture 1.15
BL Thomas cohort NA
BL Panea cohort NA

Mutation pattern and selective pressure estimates

Entity aSHM Significant selection dN/dS (missense) dN/dS (nonsense)
BL No No 1.893 0
DLBCL No No 0.000 0
FL No No 0.000 0

View coding variants in ProteinPaint hg19 or hg38

View all variants in GenomePaint hg19 or hg38

CCT6B Expression

Representative Mutation

Although well supported in the data, this mutation is clearly germline

All Mutations

1096 1102 508 515 670

References