MAGEC1

History

%%{init: { 'logLevel': 'debug', 'theme': 'dark' } }%% timeline title Publication timing 2023-07-26 : Russler : FL

Relevance tier by entity

Entity Tier Description
FL 2 relevance in FL not firmly established

Mutation incidence in large patient cohorts (GAMBL reanalysis)

Entity source frequency (%)
FL GAMBL genomes 1.85

Mutation pattern and selective pressure estimates

Entity aSHM Significant selection dN/dS (missense) dN/dS (nonsense)
BL No Yes 26.895 0.000
DLBCL No No 1.032 4.703
FL No No 0.000 0.000

## MAGEC1 Hotspots

Chromosome Coordinate (hg19) ref>alt HGVSp
chrX 140993821 T>G L211V
chrX 140993827 A>C I213L
chrX 140994066 G>C Q292H
chrX 140994280 A>G T364A

View coding variants in ProteinPaint hg19 or hg38

View all variants in GenomePaint hg19 or hg38

MAGEC1 Expression

References

  1. Russler-Germain DA, Krysiak K, Ramirez CA, Mosior M, Watkins MP, Gomez F, Skidmore ZL, Trani L, Gao F, Geyer S, Cashen A, Mehta-Shah N, Kahl B, Bartlett N, Alderuccio J, Lossos I, Ondrejka S, Hsi E, Martin P, Leonard J, Griffith M, Griffith O, Fehniger T. Mutations associated with progression in follicular lymphoma predict inferior outcomes at diagnosis: Alliance A151303. Blood Advances. 2023;7:5524–5539.