| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 35101 | BAA01g23470 | A01 | 12109746 | C | T | downstream_gene_variant | MODIFIER | c.*4664G>A| |
S48 |
| 35102 | BAA01g23470 | A01 | 12110077 | C | T | downstream_gene_variant | MODIFIER | c.*4333G>A| |
S36 |
| 35103 | BAA01g23470 | A01 | 12110314 | G | A | downstream_gene_variant | MODIFIER | c.*4096C>T| |
S262 |
| 35104 | BAA01g23470 | A01 | 12110783 | G | A | downstream_gene_variant | MODIFIER | c.*3627C>T| |
S37 |
| 35105 | BAA01g23470 | A01 | 12110967 | C | T | downstream_gene_variant | MODIFIER | c.*3443G>A| |
S273 |
| 35106 | BAA01g23470 | A01 | 12111024 | G | A | downstream_gene_variant | MODIFIER | c.*3386C>T| |
S262 |
| 35107 | BAA01g23470 | A01 | 12113162 | C | T | downstream_gene_variant | MODIFIER | c.*1248G>A| |
S182 |
| 35108 | BAA01g23470 | A01 | 12117166 | C | T | upstream_gene_variant | MODIFIER | c.-1833G>A| |
S44 |
| 35109 | BAA01g23470 | A01 | 12117413 | C | T | upstream_gene_variant | MODIFIER | c.-2080G>A| |
S192 |
| 35110 | BAA01g23470 | A01 | 12118100 | G | A | upstream_gene_variant | MODIFIER | c.-2767C>T| |
S246 |
| 35111 | BAA01g23470 | A01 | 12118190 | C | T | upstream_gene_variant | MODIFIER | c.-2857G>A| |
S270 |
| 35112 | BAA01g23470 | A01 | 12118278 | C | T | upstream_gene_variant | MODIFIER | c.-2945G>A| |
S306 S308 |
| 35113 | BAA01g23470 | A01 | 12118309 | G | A | upstream_gene_variant | MODIFIER | c.-2976C>T| |
S274 |
| 35114 | BAA01g23470 | A01 | 12118913 | G | A | upstream_gene_variant | MODIFIER | c.-3580C>T| |
S163 |
| 35115 | BAA01g23470 | A01 | 12119429 | G | A | upstream_gene_variant | MODIFIER | c.-4096C>T| |
S203 |
| 35116 | BAA01g23470 | A01 | 12119477 | C | T | upstream_gene_variant | MODIFIER | c.-4144G>A| |
S231 |
| 35117 | BAA01g23480 | A01 | 12121031 | G | A | downstream_gene_variant | MODIFIER | c.*253C>T| |
S257 |
| 35118 | BAA01g23480 | A01 | 12121373 | C | T | missense_variant | MODERATE | c.235G>A|p.Val79Ile |
S107 |
| 35119 | BAA01g23480 | A01 | 12121649 | C | T | intron_variant | MODIFIER | c.97+110G>A| |
S62 |
| 35120 | BAA01g23480 | A01 | 12122341 | T | A | upstream_gene_variant | MODIFIER | c.-486A>T| |
S189 |
| 35121 | BAA01g23480 | A01 | 12122359 | C | T | upstream_gene_variant | MODIFIER | c.-504G>A| |
S211 S227 |
| 35122 | BAA01g23480 | A01 | 12122554 | C | T | upstream_gene_variant | MODIFIER | c.-699G>A| |
S153 |
| 35123 | BAA01g23480 | A01 | 12123169 | C | T | upstream_gene_variant | MODIFIER | c.-1314G>A| |
S211 |
| 35124 | BAA01g23480 | A01 | 12126509 | C | T | upstream_gene_variant | MODIFIER | c.-4654G>A| |
S146 |
| 35125 | BAA01g23480 | A01 | 12126778 | C | T | upstream_gene_variant | MODIFIER | c.-4923G>A| |
S234 |