| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 164201 | BAA02g10750 | A02 | 4815537 | G | A | upstream_gene_variant | MODIFIER | c.-483C>T| |
S161 |
| 164202 | BAA02g10750 | A02 | 4816037 | C | T | upstream_gene_variant | MODIFIER | c.-983G>A| |
S128 |
| 164203 | BAA02g10750 | A02 | 4816288 | G | A | upstream_gene_variant | MODIFIER | c.-1234C>T| |
S133 |
| 164204 | BAA02g10750 | A02 | 4816946 | G | A | upstream_gene_variant | MODIFIER | c.-1892C>T| |
S159 S243 |
| 164205 | BAA02g10770 | A02 | 4817496 | C | T | missense_variant | MODERATE | c.571G>A|p.Asp191Asn |
S33 |
| 164206 | BAA02g10770 | A02 | 4817846 | G | A | missense_variant | MODERATE | c.221C>T|p.Ser74Leu |
S244 |
| 164207 | BAA02g10750 | A02 | 4818376 | C | T | upstream_gene_variant | MODIFIER | c.-3322G>A| |
S249 |
| 164208 | BAA02g10750 | A02 | 4819663 | G | A | upstream_gene_variant | MODIFIER | c.-4609C>T| |
S247 |
| 164209 | BAA02g10770 | A02 | 4820066 | G | A | upstream_gene_variant | MODIFIER | c.-2000C>T| |
S37 |
| 164210 | BAA02g10770 | A02 | 4820284 | C | T | upstream_gene_variant | MODIFIER | c.-2218G>A| |
S129 |
| 164211 | BAA02g10770 | A02 | 4820303 | G | A | upstream_gene_variant | MODIFIER | c.-2237C>T| |
S236 |
| 164212 | BAA02g10780 | A02 | 4822326 | C | T | missense_variant | MODERATE | c.333G>A|p.Met111Ile |
S19 |
| 164213 | BAA02g10770 | A02 | 4822708 | C | T | upstream_gene_variant | MODIFIER | c.-4642G>A| |
S278 |
| 164214 | BAA02g10780 | A02 | 4823257 | G | A | upstream_gene_variant | MODIFIER | c.-599C>T| |
S17 |
| 164215 | BAA02g10780 | A02 | 4824111 | T | A | upstream_gene_variant | MODIFIER | c.-1453A>T| |
S28 |
| 164216 | BAA02g10780 | A02 | 4824729 | G | A | upstream_gene_variant | MODIFIER | c.-2071C>T| |
S125 |
| 164217 | BAA02g10790 | A02 | 4826213 | G | A | missense_variant | MODERATE | c.317G>A|p.Arg106Lys |
S53 |
| 164218 | BAA02g10780 | A02 | 4827421 | C | T | upstream_gene_variant | MODIFIER | c.-4763G>A| |
S277 |
| 164219 | BAA02g10790 | A02 | 4827474 | C | T | missense_variant | MODERATE | c.1334C>T|p.Pro445Leu |
S299 |
| 164220 | BAA02g10790 | A02 | 4827605 | C | T | missense_variant | MODERATE | c.1465C>T|p.Pro489Ser |
S171 |
| 164221 | BAA02g10790 | A02 | 4828153 | C | T | synonymous_variant | LOW | c.2013C>T|p.Ile671Ile |
S157 |
| 164222 | BAA02g10790 | A02 | 4828307 | C | T | missense_variant | MODERATE | c.2167C>T|p.Leu723Phe |
S32 |
| 164223 | BAA02g10790 | A02 | 4828363 | C | T | synonymous_variant | LOW | c.2223C>T|p.Ile741Ile |
S255 |
| 164224 | BAA02g10800 | A02 | 4829316 | C | T | upstream_gene_variant | MODIFIER | c.-973C>T| |
S270 |
| 164225 | BAA02g10800 | A02 | 4829342 | C | T | upstream_gene_variant | MODIFIER | c.-947C>T| |
S171 |