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. 2012 Apr 30;7(4):e36084. doi: 10.1371/journal.pone.0036084

Table 1. KRAS mutations in 300 consecutive samples analyzed by Sanger sequencing and ASLNAqPCR.

Tissue KRAS No amplifiable DNA
Mutated by SSEQ (%) Mutated by ASLNA (%) SSEQ (%) ASLNA (%)
COLON CRC ( n = 234) 80/209 (38.3) 94/221 (44.8) 25/234 (10.7) 13/234 (5.6)
Primary (n = 163) 56/146 (38.4) 69/153 (45.1) 17/163 (10.4) 10/163 (6.1)
Metastatic (n = 71) 24/63 (38.1) 25/68 (36.7) 8/71 (11.3) 3/71 (4.2)
LUNG NSCLC ( n = 38) 16/38 (42.1) 17/37 (45.9) 0/38 (0) 1/38 (0)
Primary (n = 29) 9/29 (31.0) 12/29 (41.4) 0/29 (0) 0/29 (0)
Metastatic (n = 9) 7/9 (77.8) 5/8 (62.5) 0/9 (0) 1/9 (11.1)
PANCREAS (n = 21) 7/21 (33.3) 6/21 (28.6) 0/21 (0) 0/21 (0)
Carcinoma (n = 9) 4/9 (44.4) 4/9 (44.4) 0/9 (0) 0/9 (0)
Cyst Fluid (n = 12) 3/12 (25.0) 2/12 (16.7) 0/12 (0) 0/12 (0)
THYROID (n = 7) 0/6 (0) 0/7 (0) 1/7 (14.3) 0/7 (0)
PTC-Classic (n = 3) 0/3 (0) 0/3 (0) 0/3 (0) 0/3 (0)
PTC-Others (n = 4) 0/3 (0) 0/4 (0) 1/4 (25) 0/4 (0)

SSEQ, Sanger sequencing; ASLNA, allele specific quantitative PCR using 3′-locked nucleic acid modified primers (ASLNAqPCR); CRC, colonic adenocarcinoma; NSCLC, lung adenocarcinoma; PTC, papillary thyroid carcinoma.