Table 2.

Variances between institutional and central laboratories

GeneTissue typeMutation present or absent (VAF % )VUS, SS, and other comments specific to the mutation identified
InstitutionCentralInstitutionCentral
FLT3      
BM BM P (14.41) FLT3 N676K, not ITD or TKD, not pathogenic and not in OSU panel 
PB PB P (3.66) FLT3 S543F, mutation not clearly pathogenic, not in OSU design 
IDH1      
PB PB P (49.71) IDH1 F32V, VUS 
IDH2      
BM BM P (40.3) IDH2 R172_H173delinsSA, complex indel 
BM BM P (2.29) IDH2 R140W, observed but below cutoff (2%) at OHSU laboratory 
DMNT3A      
PB PB P (44.20) DNMT3A SS 855+1G>A, SS calls are excluded in OSU panel 
BM BM P (50.00) DNMT3A G156E, VUS 
PB PB P (44.26) DNMT3A SS 2478+1G>A, SS calls are excluded in OSU panel 
BM BM P (20.2) DNMT3A R379C, VUS, low tumor purity at central laboratory 
TET2      
BM BM P (49.6) TET2 S1039L, benign SNP 
BM BM P (82.78) TET2 SS 4044+1G>A, SS calls are excluded in OSU panel 
BM BM P (47.0) TET2 I1873T, reported as a somatic pathogenic variant 
BM BM P (45.0, 49.0) TET2 I1873T, reported as a somatic pathogenic variant (45%); R814C is likely germ line variant (49%) 
WT1      
BM BM P (4.20) WT1 A382fs, VUS 
PB PB P (53.56) WT1 A5V, benign SNP 
BM BM P (52.82) WT1 G6OR, area not covered on OSU panel 
BM PB P (3.00) WT1 R462Q, tissue mismatch 
TP53      
BM BM P (10.37) TP53 P153fs, likely artifact owing to large insertion 
PB PB P (46.6) TP53 R205Q, VUS 
PB PB P (2.3) TP53 C124R, below cutoff at central laboratory 
PB PB P (3.44) TP53 L194R, below cutoff at institution laboratory (OSU) 
BM BM P (10.8) TP53 G245S, suboptimal tumor purity and sample quality at central laboratory 
PB PB P (69.55) TP53 C215G, area not covered on OSU panel 
BM BM P (49.85) TP53 T125T, detected by local laboratory (OHSU) but filtered as a synonymous variant. 
GeneTissue typeMutation present or absent (VAF % )VUS, SS, and other comments specific to the mutation identified
InstitutionCentralInstitutionCentral
FLT3      
BM BM P (14.41) FLT3 N676K, not ITD or TKD, not pathogenic and not in OSU panel 
PB PB P (3.66) FLT3 S543F, mutation not clearly pathogenic, not in OSU design 
IDH1      
PB PB P (49.71) IDH1 F32V, VUS 
IDH2      
BM BM P (40.3) IDH2 R172_H173delinsSA, complex indel 
BM BM P (2.29) IDH2 R140W, observed but below cutoff (2%) at OHSU laboratory 
DMNT3A      
PB PB P (44.20) DNMT3A SS 855+1G>A, SS calls are excluded in OSU panel 
BM BM P (50.00) DNMT3A G156E, VUS 
PB PB P (44.26) DNMT3A SS 2478+1G>A, SS calls are excluded in OSU panel 
BM BM P (20.2) DNMT3A R379C, VUS, low tumor purity at central laboratory 
TET2      
BM BM P (49.6) TET2 S1039L, benign SNP 
BM BM P (82.78) TET2 SS 4044+1G>A, SS calls are excluded in OSU panel 
BM BM P (47.0) TET2 I1873T, reported as a somatic pathogenic variant 
BM BM P (45.0, 49.0) TET2 I1873T, reported as a somatic pathogenic variant (45%); R814C is likely germ line variant (49%) 
WT1      
BM BM P (4.20) WT1 A382fs, VUS 
PB PB P (53.56) WT1 A5V, benign SNP 
BM BM P (52.82) WT1 G6OR, area not covered on OSU panel 
BM PB P (3.00) WT1 R462Q, tissue mismatch 
TP53      
BM BM P (10.37) TP53 P153fs, likely artifact owing to large insertion 
PB PB P (46.6) TP53 R205Q, VUS 
PB PB P (2.3) TP53 C124R, below cutoff at central laboratory 
PB PB P (3.44) TP53 L194R, below cutoff at institution laboratory (OSU) 
BM BM P (10.8) TP53 G245S, suboptimal tumor purity and sample quality at central laboratory 
PB PB P (69.55) TP53 C215G, area not covered on OSU panel 
BM BM P (49.85) TP53 T125T, detected by local laboratory (OHSU) but filtered as a synonymous variant. 

A, absent; SS, splice site; P, present.

†VAF % cutoff value for OSU is 2.0 and for FMI is 2.0.

Assume absent of mutation is equivalent to 0.00 VAF % unless otherwise specified.

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