[CCDC42BPB]

Mutation tier

Entity Tier Description
FL 2 relevance in FL not firmly established

Mutation incidence

Entity source frequency (%)
FL GAMBL genomes NA

Mutation pattern

Entity aSHM Significant selection dN/dS (missense) dN/dS (nonsense)

[!NOTE] View coding variants in ProteinPaint hg19 or hg38

View all variants in GenomePaint hg19 or hg38

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