| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 152601 | BAA02g01170 | A02 | 551079 | G | A | missense_variant | MODERATE | c.196G>A|p.Glu66Lys |
S25 |
| 152602 | BAA02g01170 | A02 | 551178 | G | A | missense_variant | MODERATE | c.295G>A|p.Gly99Arg |
S111 S129 |
| 152603 | BAA02g01170 | A02 | 551191 | C | T | missense_variant | MODERATE | c.308C>T|p.Thr103Ile |
S211 |
| 152604 | BAA02g01170 | A02 | 552476 | C | T | missense_variant | MODERATE | c.907C>T|p.Leu303Phe |
S82 S92 |
| 152605 | BAA02g01160 | A02 | 553301 | G | A | upstream_gene_variant | MODIFIER | c.-4620C>T| |
S246 |
| 152606 | BAA02g01170 | A02 | 553413 | G | A | synonymous_variant | LOW | c.1434G>A|p.Glu478Glu |
S4 |
| 152607 | BAA02g01180 | A02 | 554208 | C | T | upstream_gene_variant | MODIFIER | c.-100C>T| |
S118 |
| 152608 | BAA02g01180 | A02 | 554809 | G | A | synonymous_variant | LOW | c.318G>A|p.Glu106Glu |
S64 |
| 152609 | BAA02g01180 | A02 | 555099 | G | A | missense_variant&splice_region_variant | MODERATE | c.418G>A|p.Val140Ile |
S5 S84 |
| 152610 | BAA02g01200 | A02 | 555207 | C | T | upstream_gene_variant | MODIFIER | c.-3592C>T| |
S278 |
| 152611 | BAA02g01190 | A02 | 555576 | C | T | missense_variant | MODERATE | c.1651G>A|p.Ala551Thr |
S142 |
| 152612 | BAA02g01190 | A02 | 556404 | C | T | missense_variant | MODERATE | c.1111G>A|p.Gly371Arg |
S278 |
| 152613 | BAA02g01200 | A02 | 557626 | G | A | upstream_gene_variant | MODIFIER | c.-1173G>A| |
S134 |
| 152614 | BAA02g01190 | A02 | 558053 | C | T | missense_variant | MODERATE | c.248G>A|p.Ser83Asn |
S274 |
| 152615 | BAA02g01190 | A02 | 558355 | C | T | missense_variant | MODERATE | c.34G>A|p.Val12Ile |
S167 |
| 152616 | BAA02g01200 | A02 | 559942 | G | A | missense_variant&splice_region_variant | MODERATE | c.839G>A|p.Gly280Glu |
S33 |
| 152617 | BAA02g01200 | A02 | 560105 | G | A | synonymous_variant | LOW | c.912G>A|p.Arg304Arg |
S87 |
| 152618 | BAA02g01200 | A02 | 560233 | C | T | missense_variant | MODERATE | c.1040C>T|p.Thr347Ile |
S277 |
| 152619 | BAA02g01190 | A02 | 560321 | G | A | upstream_gene_variant | MODIFIER | c.-1933C>T| |
S168 |
| 152620 | BAA02g01190 | A02 | 560390 | G | A | upstream_gene_variant | MODIFIER | c.-2002C>T| |
S136 |
| 152621 | BAA02g01190 | A02 | 560777 | G | A | upstream_gene_variant | MODIFIER | c.-2389C>T| |
S51 |
| 152622 | BAA02g01190 | A02 | 560896 | G | C | upstream_gene_variant | MODIFIER | c.-2508C>G| |
S170 |
| 152623 | BAA02g01190 | A02 | 562312 | G | A | upstream_gene_variant | MODIFIER | c.-3924C>T| |
S208 S93 |
| 152624 | BAA02g01190 | A02 | 562535 | C | T | upstream_gene_variant | MODIFIER | c.-4147G>A| |
S8 |
| 152625 | BAA02g01190 | A02 | 563321 | C | T | upstream_gene_variant | MODIFIER | c.-4933G>A| |
S179 |