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Its prevalence is mainly in Caucasians (about 5%), and this mutation is absent in Africans and Asians.
The BRAF V600E mutation is absent.
The BRAF V600E mutation is absent in SRPL.
However, this mutation is absent in primary total atherosclerotic lesion.
# Mutation is absent and also the region has not been annotated as ORF.
This mutation is absent in other DLBCL subtypes, including germinal centre B-cell-like DLBCL and Burkitt's lymphoma.
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In the case of VapA, this level was approximately 15 to 30-fold higher than the level of VapA present in cells where the nuclear mutation was absent.
The mutation co-segregated with the phenotype, as the mutation was absent from blood and muscle in the patient's healthy mother.
The mutation was absent from >140 healthy control individuals.
A lower frequency of haplotypes HHB (0.04) and HHF1 (0.09) was observed and HHG2 (bearing the Δ32 mutation) was absent (Figure 2).
In the first study, a mutation affecting the DIA1R signal peptide (a change of serine at position 24 to proline or 'S24P', using single amino acid abbreviations) was reported in a single XLMR patient, while the same mutation was absent in controls [122].
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