S. No / Locus / Gene / Base change / Ref. Sequence / Codon No. / Codon Position / Codon change / Amino acid changes
1 / 6023 / G>A / G / 40 / 3 / GAG>GAA / Glu>Glu
2 / 6026 / G>A / G / 41 / 3 / CTG>CTA / Lue>Lue
3 / 6029 / C>T / C / 42 / 3 / GGC> GTG / Gly>Gly
4 / 6032 / G>A / G / 43 / 3 / CAG> CAA / Gln>Gln
5 / 6035 / A>T / A / 44 / 3 / CCA> CCT / Pro>Pro
6 / 6071 / T>C / T / 56 / 3 / GTT> GTC / Val>VAl
7 / 6086 / T>C / T / 61 / 3 / CAT> CTC / His>His
8 / 6092 / T>C / T / 63 / 3 / TTT> TTC / Phe>Phe
9 / 6104 / C>T / C / 67 / 3 / TTC> TTT / Phy>Phy
10 / 6116 / A>G / A / 71 / 3 / ATA> ATG / Ile>Met
11 / 6128 / C>T / C / 75 / 3 / ATC> ATT / Ile>Ile
12 / 6134 / C>T / C / 77 / 3 / GGC>GGT / Gly>Gly
13 / 6143 / C>T / C / 80 / 3 / AAC>AAT / Asn>Asn
14 / 6149 / A>G / A / 82 / 3 / CTA>CTG / Leu>Leu
15 / 6152 / T>C / T / 83 / 3 / GTT>GTC / Val>Val
16 / 6158 / A>G / A / 85 / 3 / CTA>CTG / Leu>Leu
17 / 6164 / C>T / C / 87 / 3 / ATC>ATT / Ile>Ile
18 / 6167 / T>C / T / 88 / 3 / GGT>GGC / Gly>Gly
19 / 6173 / C>T / C / 90 / 3 / CCC>CCT / Pro>Pro
20 / 6176 / T>C / T / 91 / 3 / GAT>GAC / Asp>Asp
21 / 6182 / G>A / G / 93 / 3 / GCG>GCA / Ala>Ala
22 / 6197 / C>T / C / 98 / 3 / AAC>AAT / Asn>Asn
23 / 6212 / A>G / A / 103 / 3 / TGA>TGG / Ssp>Trp
24
25 / 6216 / *6218 / T>C and A>T / T and A / 105 / 1 and 3 / TTA>CTT / Leu>Leu
26 / 6221 / T>C / T / 106 / 3 / CCT>CCC / Pro>Pro
27 / *6236 / C>A / C / 111 / 3 / CTC>CTA / Leu>Leu
28 / 6242 / C>G / C / 113 / 3 / CTC>CTG / Leu>Leu
29 / 6260 / G>A / G / 119 / 3 / GAG>GAA / Glu>Glu
30 / 6263 / C>T / C / 120 / 3 / GCC>GCT / Ala>Ala
31 / * 6266 / A>T / A / 121 / 3 / GGA>GGT / Gly>Gly
32 / *6269 / A>C / A / 122 / 3 / GCA>GCC / Ala>Ala
33 / 6284 / A>G / A / 127 / 3 / ACA>ACG / Thr>Thr
34 / 6287 / C>T / C / 128 / 3 / GTC>GTT / Val>Val
35 / 6296 / C>T / C / 131 / 3 / CCC>CCT / Pro>Pro
36 / 6299 / A>G / A / 133 / 3 / TTA>TTG / Leu>Leu
37 / 6305 / G>A / G / 134 / 3 / GGG>GGA / Gly>Gly
38 / 6311 / C>T / C / 136 / 3 / TAC>TAT / Tyr>Tyr
39 / 6317 / C>T / C / 138 / 3 / CAC>CAT / His>His
40 / *6320 / T>A / T / 139 / 3 / CCT>CCA / Pro>Pro
41 / 6329 / C>T / C / 142 / 3 / TCC>TCT / Ser>Ser
42 / *6344 / C>T / C / 147 / 3 / ATC>ATT / Ile>Ile
43
44 / 6351 / *6353 / T>C and A>T / T and A / 150 / 1 and 3 / TTA>CTT / Leu>Leu
45 / *6356 / C>T / C / 151 / 3 / CAC>CAT / His>His
46 / 6377 / C>T / C / 158 / 3 / ATC>ATT / Ile>Ile
47 / 6378 / T>C / T / 159 / 1 / TTA>CTA / Leu>Leu
48 / 6383 / G>A / G / 160 / 3 / GGG>GGA / Gly>Gly
49 / 6386 / C>T / C / 161 / 3 / GCC>GCT / Ala>Ala
50 / 6389 / C>T / C / 162 / 3 / ATC>ATT / Ile>Ile
51 / *6401 / A>C / A / 166 / 3 / ACA>ACC / Thr>Thr
52 / 6410 / C>T / C / 169 / 3 / ATC>ATT / Ile>Ile
53 / 6413 / T>C / T / 170 / 3 / AAT>AAC / Asn>Asn
54 / 6455 / C>T / C / 184 / 3 / TTC>TTT / Phe>Phe
55 / 6464 / C>T / C / 187 / 3 / TCC>TCT / Ser>Ser
56 / 6476 / A>G / A / 191 / 3 / ACA>ACG / Thr>Thr
57 / 6488 / T>C / T / 195 / 3 / CTT>CTC / Leu>Leu
58 / * 6494 / A>C / A / 197 / 3 / CTA>CTC / Leu>Leu
59 / 6497 / T>C / T / 198 / 3 / TCT>TCC / Ser>ser
60 / 6500 / C>T / C / 199 / 3 / CTC>CTT / Leu>Leu
61
62 / *6507 / 6509 / C>T and A>G / C and A / 202 / 1 and 3 / CTA>TTG / Leu>Leu
63 / 6512 / T>C / T / 203 / 3 / GCT>GCC / Ala>Ala
64 / 6521 / C>T / C / 206 / 3 / ATC>ATT / Ile>Ile
65 / 6530 / A>G / A / 209 / 3 / CTA>CTG / Leu>Leu
66 / 6542 / C>T / C / 213 / 3 / CGC>CGT / Arg>Arg
67 / 6548 / C>T / C / 215 / 3 / CTC>CTT / Leu>Leu
68 / 6560 / C>T / C / 219 / 3 / AAC>AAT / Asn>Asn

Supplementary Table 1: Synonymous variation of COXI region of cancer sequences.

* represents new reported variation and mutations.