| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 11501 | BAA01g09250-BAA01g09260 | A01 | 4097844 | C | T | intergenic_region | MODIFIER | n.4097844C>T| |
S153 S213 |
| 11502 | BAA01g09250-BAA01g09260 | A01 | 4101447 | G | A | intergenic_region | MODIFIER | n.4101447G>A| |
S172 |
| 11503 | BAA01g09250-BAA01g09260 | A01 | 4101625 | G | A | intergenic_region | MODIFIER | n.4101625G>A| |
S271 |
| 11504 | BAA01g09260 | A01 | 4102273 | C | T | downstream_gene_variant | MODIFIER | c.*4611G>A| |
S244 |
| 11505 | BAA01g09260 | A01 | 4103046 | C | T | downstream_gene_variant | MODIFIER | c.*3838G>A| |
S280 |
| 11506 | BAA01g09260 | A01 | 4104053 | A | T | downstream_gene_variant | MODIFIER | c.*2831T>A| |
S18 S221 S293 S294 |
| 11507 | BAA01g09260 | A01 | 4104860 | C | T | downstream_gene_variant | MODIFIER | c.*2024G>A| |
S268 |
| 11508 | BAA01g09260 | A01 | 4104880 | C | T | downstream_gene_variant | MODIFIER | c.*2004G>A| |
S189 |
| 11509 | BAA01g09260 | A01 | 4104917 | C | T | downstream_gene_variant | MODIFIER | c.*1967G>A| |
S192 |
| 11510 | BAA01g09260 | A01 | 4105242 | C | T | downstream_gene_variant | MODIFIER | c.*1642G>A| |
S40 S49 |
| 11511 | BAA01g09260 | A01 | 4107794 | G | A | synonymous_variant | LOW | c.507C>T|p.Leu169Leu |
S274 |
| 11512 | BAA01g09260 | A01 | 4109044 | C | T | upstream_gene_variant | MODIFIER | c.-421G>A| |
S202 |
| 11513 | BAA01g09260 | A01 | 4109087 | G | A | upstream_gene_variant | MODIFIER | c.-464C>T| |
S241 |
| 11514 | BAA01g09260 | A01 | 4110666 | G | A | upstream_gene_variant | MODIFIER | c.-2043C>T| |
S247 |
| 11515 | BAA01g09260 | A01 | 4110969 | G | A | upstream_gene_variant | MODIFIER | c.-2346C>T| |
S306 S308 |
| 11516 | BAA01g09260 | A01 | 4111330 | G | A | upstream_gene_variant | MODIFIER | c.-2707C>T| |
S191 |
| 11517 | BAA01g09260 | A01 | 4111973 | G | A | upstream_gene_variant | MODIFIER | c.-3350C>T| |
S114 |
| 11518 | BAA01g09270 | A01 | 4112373 | C | T | missense_variant | MODERATE | c.1042G>A|p.Glu348Lys |
S53 |
| 11519 | BAA01g09270 | A01 | 4113111 | G | A | missense_variant | MODERATE | c.1004C>T|p.Pro335Leu |
S133 |
| 11520 | BAA01g09260 | A01 | 4113214 | C | T | upstream_gene_variant | MODIFIER | c.-4591G>A| |
S70 |
| 11521 | BAA01g09270 | A01 | 4114394 | G | A | intron_variant | MODIFIER | c.775-237C>T| |
S289 S290 |
| 11522 | BAA01g09270 | A01 | 4115515 | G | A | intron_variant | MODIFIER | c.312-52C>T| |
S199 |
| 11523 | BAA01g09270 | A01 | 4115789 | G | A | synonymous_variant | LOW | c.249C>T|p.Leu83Leu |
S92 |
| 11524 | BAA01g09270 | A01 | 4115966 | G | A | synonymous_variant | LOW | c.72C>T|p.Asn24Asn |
S242 |
| 11525 | BAA01g09270 | A01 | 4116686 | C | T | upstream_gene_variant | MODIFIER | c.-649G>A| |
S244 |