| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 81451 | BAA01g43110 | A01 | 28516556 | C | T | upstream_gene_variant | MODIFIER | c.-4746G>A| |
S32 |
| 81452 | BAA01g43110 | A01 | 28516673 | G | A | upstream_gene_variant | MODIFIER | c.-4863C>T| |
S71 |
| 81453 | BAA01g43130 | A01 | 28517192 | G | A | downstream_gene_variant | MODIFIER | c.*4831C>T| |
S226 |
| 81454 | BAA01g43130 | A01 | 28517227 | G | A | downstream_gene_variant | MODIFIER | c.*4796C>T| |
S169 |
| 81455 | BAA01g43130 | A01 | 28517792 | G | A | downstream_gene_variant | MODIFIER | c.*4231C>T| |
S280 |
| 81456 | BAA01g43120 | A01 | 28517885 | G | A | synonymous_variant | LOW | c.327C>T|p.Cys109Cys |
S2 |
| 81457 | BAA01g43120 | A01 | 28517980 | C | T | missense_variant | MODERATE | c.232G>A|p.Ala78Thr |
S48 |
| 81458 | BAA01g43130 | A01 | 28518247 | A | T | downstream_gene_variant | MODIFIER | c.*3776T>A| |
S139 |
| 81459 | BAA01g43130 | A01 | 28518250 | G | A | downstream_gene_variant | MODIFIER | c.*3773C>T| |
S139 |
| 81460 | BAA01g43120 | A01 | 28518646 | C | T | upstream_gene_variant | MODIFIER | c.-185G>A| |
S183 S198 |
| 81461 | BAA01g43120 | A01 | 28518753 | C | T | upstream_gene_variant | MODIFIER | c.-292G>A| |
S132 S215 S89 |
| 81462 | BAA01g43120 | A01 | 28518904 | G | A | upstream_gene_variant | MODIFIER | c.-443C>T| |
S294 |
| 81463 | BAA01g43120 | A01 | 28519346 | G | A | upstream_gene_variant | MODIFIER | c.-885C>T| |
S43 |
| 81464 | BAA01g43120 | A01 | 28520506 | T | C | upstream_gene_variant | MODIFIER | c.-2045A>G| |
S6 |
| 81465 | BAA01g43120 | A01 | 28521691 | C | T | upstream_gene_variant | MODIFIER | c.-3230G>A| |
S94 |
| 81466 | BAA01g43130 | A01 | 28522470 | C | T | missense_variant | MODERATE | c.1171G>A|p.Val391Met |
S32 |
| 81467 | BAA01g43130 | A01 | 28522596 | G | A | missense_variant | MODERATE | c.1045C>T|p.Pro349Ser |
S286 |
| 81468 | BAA01g43130 | A01 | 28522982 | G | A | missense_variant | MODERATE | c.659C>T|p.Ser220Phe |
S87 |
| 81469 | BAA01g43130 | A01 | 28523024 | G | A | missense_variant | MODERATE | c.617C>T|p.Pro206Leu |
S226 |
| 81470 | BAA01g43130 | A01 | 28523626 | C | T | missense_variant | MODERATE | c.226G>A|p.Glu76Lys |
S67 |
| 81471 | BAA01g43130 | A01 | 28523736 | C | T | missense_variant | MODERATE | c.116G>A|p.Gly39Glu |
S192 |
| 81472 | BAA01g43140 | A01 | 28523819 | G | A | downstream_gene_variant | MODIFIER | c.*927C>T| |
S251 |
| 81473 | BAA01g43140 | A01 | 28524819 | G | A | missense_variant | MODERATE | c.392C>T|p.Pro131Leu |
S151 S263 |
| 81474 | BAA01g43150 | A01 | 28527145 | C | T | missense_variant | MODERATE | c.1405G>A|p.Glu469Lys |
S88 |
| 81475 | BAA01g43150 | A01 | 28527794 | C | T | synonymous_variant | LOW | c.756G>A|p.Leu252Leu |
S169 |