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. 2017 Dec 23;109(1):225–230. doi: 10.1111/cas.13450

Table 1.

Targeted sequencing of MYD88 L265P for 14 PCNSL samples

Mutation ratio of MYD88 L265P (%)
Tumors Cell‐free DNAs in serum
NGS ddPCR NGS ddPCR
VAF (%) Reads showing the mutation/total reads FA (%) VAF Reads showing the mutation/total reads FA (%)
TP73 43.2 8584/19870 ND 0 0/19996 0
TP87 65.5 13070/19954 ND 0 0/19930 0.40
TP89 35.1 6979/19882 ND 0 0/19981 0.19
TP90 40.9 8137/19895 ND 0 0/19980 0.09
TP92 53.3 10534/19763 ND 0 0/19985 0.10
TP94 61.3 12233/19956 ND 0 0/19948 0.38
TP95 36.4 7230/19862 ND 0 0/19963 0.14
TP96 56.1 11122/19825 ND 0 0/19972 0.47
TP98 88.7 17736/19993 87 0 0/19987 0
TP99 56.6 11299/19974 55.9 0 0/19994 0.69
TP100 75.2 15025/19980 79 ND ND 0
TP101 9.2 1844/19988 10.5 0 0/12560 0
TP102 43 7260/16868 38.3 0 0/19991 0
TP103 19.7 3928/19973 17.1 0 0/19989 0

ddPCR, droplet digital PCR; FA, fractional abundance; ND, not done; NGS, next‐generation sequencing; PCNSL, primary central nervous system lymphoma; VAF, variant allele frequency.