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. Author manuscript; available in PMC: 2020 Jan 1.
Published in final edited form as: Surgery. 2018 Oct 22;165(1):17–24. doi: 10.1016/j.surg.2018.04.062

Table 2.

Low allelic frequency and low malignancy risk mutations on ThyroSeq v2 considered to be “ThyroSeq negative” by institution. MSKCC, Memorial Sloan-Kettering Cancer Center; MCC, Moffitt Cancer Center; CSMC, Cedars-Sinai Medical Center; MSHS, Mount Sinai Health System.

MSKCC
(n=7)
MCC
(n=11)
CSMC
(n=0)
MSHS
(n=3)
Malignant
n (%)
“Benign” mutations
  NIS overexpression (n=1) 1 0
  PTH expression (n=2) 1 1 0
Low allelic frequency mutations
  EIF1AX (n=2) 1 1 0
  PTEN (n=1) 1 0
  RAS (n=11) 4 6 1 2(18)
  TERT promoter (n=1) 1 0
  TP53 indeterminate* (n=1) 1 0
  TSHR (n=2) 1 1 0
Malignant, n (%) 1 (14) 1 (9) 0 0 2 (10)
*

Indeterminate due to poor quality sequencing, suspicious for low allelic fraction mutation.