| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 152501 | BAA02g01080 | A02 | 509204 | G | A | downstream_gene_variant | MODIFIER | c.*1552G>A| |
S129 |
| 152502 | BAA02g01080 | A02 | 509457 | C | T | downstream_gene_variant | MODIFIER | c.*1805C>T| |
S2 |
| 152503 | BAA02g01080 | A02 | 510730 | C | T | downstream_gene_variant | MODIFIER | c.*3078C>T| |
S117 |
| 152504 | BAA02g01080 | A02 | 511090 | C | T | downstream_gene_variant | MODIFIER | c.*3438C>T| |
S2 |
| 152505 | BAA02g01090 | A02 | 515043 | G | A | upstream_gene_variant | MODIFIER | c.-2183G>A| |
S202 |
| 152506 | BAA02g01090 | A02 | 516155 | A | C | upstream_gene_variant | MODIFIER | c.-1071A>C| |
S172 S217 |
| 152507 | BAA02g01100 | A02 | 517533 | C | T | downstream_gene_variant | MODIFIER | c.*2965G>A| |
S77 S82 |
| 152508 | BAA02g01090 | A02 | 519165 | C | T | downstream_gene_variant | MODIFIER | c.*1084C>T| |
S70 |
| 152509 | BAA02g01100 | A02 | 520559 | G | A | missense_variant | MODERATE | c.539C>T|p.Thr180Ile |
S223 |
| 152510 | BAA02g01100 | A02 | 521461 | C | T | upstream_gene_variant | MODIFIER | c.-273G>A| |
S267 |
| 152511 | BAA02g01100 | A02 | 522179 | A | G | upstream_gene_variant | MODIFIER | c.-991T>C| |
S249 |
| 152512 | BAA02g01100 | A02 | 523075 | C | T | upstream_gene_variant | MODIFIER | c.-1887G>A| |
S40 S49 |
| 152513 | BAA02g01100 | A02 | 523581 | C | T | upstream_gene_variant | MODIFIER | c.-2393G>A| |
S142 |
| 152514 | BAA02g01100 | A02 | 524055 | G | A | upstream_gene_variant | MODIFIER | c.-2867C>T| |
S273 |
| 152515 | BAA02g01100 | A02 | 524192 | G | A | upstream_gene_variant | MODIFIER | c.-3004C>T| |
S265 |
| 152516 | BAA02g01100 | A02 | 525006 | G | A | upstream_gene_variant | MODIFIER | c.-3818C>T| |
S173 |
| 152517 | BAA02g01100 | A02 | 526014 | C | T | upstream_gene_variant | MODIFIER | c.-4826G>A| |
S207 |
| 152518 | BAA02g01110 | A02 | 527667 | C | T | upstream_gene_variant | MODIFIER | c.-1262C>T| |
S267 |
| 152519 | BAA02g01120 | A02 | 531765 | C | T | missense_variant | MODERATE | c.1858G>A|p.Asp620Asn |
S83 S88 |
| 152520 | BAA02g01120 | A02 | 532756 | A | G | synonymous_variant | LOW | c.867T>C|p.Leu289Leu |
S142 |
| 152521 | BAA02g01120 | A02 | 533080 | C | T | synonymous_variant | LOW | c.543G>A|p.Val181Val |
S112 |
| 152522 | BAA02g01120 | A02 | 533392 | G | A | synonymous_variant | LOW | c.231C>T|p.Phe77Phe |
S153 S213 |
| 152523 | BAA02g01120 | A02 | 533894 | G | A | upstream_gene_variant | MODIFIER | c.-272C>T| |
S162 |
| 152524 | BAA02g01130 | A02 | 534949 | C | T | synonymous_variant | LOW | c.936G>A|p.Ala312Ala |
S201 |
| 152525 | BAA02g01120 | A02 | 535052 | C | T | upstream_gene_variant | MODIFIER | c.-1430G>A| |
S177 |