| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 195001 | BAA02g28320 | A02 | 15907397 | C | T | downstream_gene_variant | MODIFIER | c.*2929C>T| |
S49 |
| 195002 | BAA02g28320 | A02 | 15907796 | G | A | downstream_gene_variant | MODIFIER | c.*3328G>A| |
S35 |
| 195003 | BAA02g28320 | A02 | 15908153 | C | T | downstream_gene_variant | MODIFIER | c.*3685C>T| |
S66 |
| 195004 | BAA02g28320 | A02 | 15908464 | G | A | downstream_gene_variant | MODIFIER | c.*3996G>A| |
S291 |
| 195005 | BAA02g28320 | A02 | 15909191 | G | A | downstream_gene_variant | MODIFIER | c.*4723G>A| |
S144 |
| 195006 | BAA02g28330 | A02 | 15909569 | C | T | downstream_gene_variant | MODIFIER | c.*3613C>T| |
S258 |
| 195007 | BAA02g28330 | A02 | 15909968 | C | T | downstream_gene_variant | MODIFIER | c.*4012C>T| |
S207 |
| 195008 | BAA02g28330 | A02 | 15910220 | C | T | downstream_gene_variant | MODIFIER | c.*4264C>T| |
S177 |
| 195009 | BAA02g28330 | A02 | 15910594 | C | T | downstream_gene_variant | MODIFIER | c.*4638C>T| |
S140 |
| 195010 | BAA02g28340 | A02 | 15911018 | C | T | downstream_gene_variant | MODIFIER | c.*1123G>A| |
S178 |
| 195011 | BAA02g28340 | A02 | 15911240 | C | T | downstream_gene_variant | MODIFIER | c.*901G>A| |
S244 |
| 195012 | BAA02g28340 | A02 | 15911864 | C | T | downstream_gene_variant | MODIFIER | c.*277G>A| |
S88 |
| 195013 | BAA02g28340 | A02 | 15911934 | C | T | downstream_gene_variant | MODIFIER | c.*207G>A| |
S284 |
| 195014 | BAA02g28340 | A02 | 15912653 | C | T | synonymous_variant | LOW | c.243G>A|p.Gly81Gly |
S265 S39 |
| 195015 | BAA02g28340 | A02 | 15913280 | C | T | upstream_gene_variant | MODIFIER | c.-385G>A| |
S131 |
| 195016 | BAA02g28340 | A02 | 15914050 | G | A | upstream_gene_variant | MODIFIER | c.-1155C>T| |
S169 |
| 195017 | BAA02g28350 | A02 | 15914504 | C | T | synonymous_variant | LOW | c.2688G>A|p.Gly896Gly |
S113 S117 S122 S266 S297 S55 S65 S9 |
| 195018 | BAA02g28350 | A02 | 15914718 | G | A | missense_variant | MODERATE | c.2474C>T|p.Ala825Val |
S256 |
| 195019 | BAA02g28350 | A02 | 15915177 | G | A | missense_variant | MODERATE | c.2015C>T|p.Ser672Phe |
S247 |
| 195020 | BAA02g28350 | A02 | 15916648 | A | C | missense_variant | MODERATE | c.544T>G|p.Ser182Ala |
S289 S290 |
| 195021 | BAA02g28340 | A02 | 15917793 | G | A | upstream_gene_variant | MODIFIER | c.-4898C>T| |
S143 |
| 195022 | BAA02g28350 | A02 | 15918361 | G | A | upstream_gene_variant | MODIFIER | c.-1170C>T| |
S23 |
| 195023 | BAA02g28350 | A02 | 15918592 | A | T | upstream_gene_variant | MODIFIER | c.-1401T>A| |
S144 |
| 195024 | BAA02g28350 | A02 | 15919149 | C | T | upstream_gene_variant | MODIFIER | c.-1958G>A| |
S255 |
| 195025 | BAA02g28350 | A02 | 15920026 | C | T | upstream_gene_variant | MODIFIER | c.-2835G>A| |
S130 |