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. 2022 Sep 2;26(6):699–713. doi: 10.1007/s40291-022-00612-3

Table 2.

Evaluation of IDH1 status received from non-reference center (MLPA), with 3 molecular methods (NGS, qPCR, Sanger) received from reference oncology center

Patient ID Non-reference center Reference oncology center
Histopathological diagnosis IDH1 status MLPA IDH1 status NGS First verification qPCRa Second verification Sanger Protein change Concordance in IDH1 status
12 A3 wt wt wt wt p= Yes
13 A2 wt Pathogenic Mutant Mutant R132Lb No*
19 A2 Mutant Pathogenic Mutant Mutant R132Hc Yes
34 A2 Mutant Pathogenic Mutant Mutant R132Hc Yes

A2/3 astrocytoma grade 2/3, IDH1 isocitrate dehydrogenase 1, MLPA multiplex ligation-dependent probe amplification to detect 4 mutant variants (R132C, R132H, R172K, R172M), NGS next-generation sequencing, p= no protein change has been detected in analyzed sample, qPCR quantitative polymerase chain reaction, wt wildtype

aIDH1/2 Mutation Analysis Kit (EntroGen) is a screening qPCR test for the detection of the most common mutations in codon 132 and 100 of the IDH1 gene and in codon 172 and 140 of the IDH2 gene. IDH1: Codon 132 (the test cannot distinguish between the following mutations: c.395G>A; c.394C>T; c.394C>A; c.394C>G; c.395G>T; c.395G>C; c.394_395delinsGT); codon 100 (c.299G>A)

bNM_005896.2:c.395G>T

cNM_005896.2:c.395G>A

*MLPA test does not detect R132L variant