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. 2015 Feb 24;10(2):e0117818. doi: 10.1371/journal.pone.0117818

Table 3. SNPs called in the HCC1954 cell line.

Gene Chromosome Position Variation
AKT1 14 105235824 rs58565216
AKT1 14 105236287 rs35416681
AKT1 14 105241304 rs2230506
CAV1 7 116200554 rs374946197
HER2 17 37855834 rs4252596
HER2 17 37869895 -
HER2 17 37870378 rs2934967
HER2 17 37871081 -
HER2 17 37876835 rs2952156
HER2 17 37877412 rs2952157
HER2 17 37877447 rs11653998
HER2 17 37878371 -
HER2 17 37878574 -
HER2 17 37878635 -
HER2 17 37879030 rs2088126
HER2 17 37884037 rs1058808, rs370420724, CM087578
HER2 17 37885332 rs2952158
IGFBP3 7 45957678 rs3793345
IGFBP3 7 45960645 rs2854746, CM057457
IL8 4 74609045 rs1126647, CR025956
MAPK1 22 22115004 rs6928
MAPK1 22 22115353 rs9340
MAPK1 22 22115498 rs3810610
MAPK1 22 22116202 rs13943
MAPK1 22 22116467 rs1063311
PIK3CA 3 178952085 rs121913279, COSM776, COSM775, COSM249874, COSM94987, COSM94986
PTGS2 1 186641626 rs2853805
PTGS2 1 186642429 rs2206593
PTGS2 1 186643058 rs5275

The table displays information about chromosomal location of the detected SNPs in the genes of interest as well as corresponding SNP ID numbers [8]. In case of missing ID numbers (‘-’), we likely inferred a novel mutation.