Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g22740 | A09 | 14302404 | C | T | upstream_gene_variant | MODIFIER | c.-2349C>T| |
S30 S31 |
2 | BAA09g22740 | A09 | 14302799 | T | G | upstream_gene_variant | MODIFIER | c.-1954T>G| |
S105 S128 S131 S149 S151 S161 S163 S206 S255 S257 S291 S296 S49 S74 S90 |
3 | BAA09g22740 | A09 | 14303051 | G | A | upstream_gene_variant | MODIFIER | c.-1702G>A| |
S289 |
4 | BAA09g22740 | A09 | 14303308 | C | T | upstream_gene_variant | MODIFIER | c.-1445C>T| |
S133 S273 |
5 | BAA09g22740 | A09 | 14303374 | G | A | upstream_gene_variant | MODIFIER | c.-1379G>A| |
S116 |
6 | BAA09g22740 | A09 | 14303586 | G | A | upstream_gene_variant | MODIFIER | c.-1167G>A| |
S129 |
7 | BAA09g22740 | A09 | 14303766 | G | A | upstream_gene_variant | MODIFIER | c.-987G>A| |
S1 S90 |
8 | BAA09g22740 | A09 | 14303841 | G | A | upstream_gene_variant | MODIFIER | c.-912G>A| |
S210 S225 |
9 | BAA09g22740 | A09 | 14303931 | G | A | upstream_gene_variant | MODIFIER | c.-822G>A| |
S180 |
10 | BAA09g22740 | A09 | 14305177 | G | A | missense_variant | MODERATE | c.316G>A|p.Ala106Thr |
S225 S73 |
11 | BAA09g22740 | A09 | 14305841 | G | A | missense_variant | MODERATE | c.485G>A|p.Gly162Glu |
S266 |
12 | BAA09g22740 | A09 | 14305919 | C | T | missense_variant | MODERATE | c.563C>T|p.Ser188Phe |
S183 |
13 | BAA09g22740 | A09 | 14306167 | G | A | missense_variant | MODERATE | c.682G>A|p.Ala228Thr |
S297 |
14 | BAA09g22740 | A09 | 14309105 | C | T | downstream_gene_variant | MODIFIER | c.*2446C>T| |
S172 S217 |
15 | BAA09g22740 | A09 | 14309397 | C | T | downstream_gene_variant | MODIFIER | c.*2738C>T| |
S64 |
16 | BAA09g22740 | A09 | 14310994 | C | T | downstream_gene_variant | MODIFIER | c.*4335C>T| |
S245 |
17 | BAA09g22740 | A09 | 14311651 | C | T | downstream_gene_variant | MODIFIER | c.*4992C>T| |
S48 |