| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA08g35600 | A08 | 22608942 | G | A | upstream_gene_variant | MODIFIER | c.-1721G>A| |
S263 |
| 2 | BAA08g35600 | A08 | 22609209 | A | G | upstream_gene_variant | MODIFIER | c.-1454A>G| |
S137 S138 S215 S237 S238 S288 |
| 3 | BAA08g35600 | A08 | 22609716 | C | T | upstream_gene_variant | MODIFIER | c.-947C>T| |
S198 |
| 4 | BAA08g35600 | A08 | 22610130 | G | A | upstream_gene_variant | MODIFIER | c.-533G>A| |
S139 |
| 5 | BAA08g35600 | A08 | 22610179 | C | T | upstream_gene_variant | MODIFIER | c.-484C>T| |
S70 |
| 6 | BAA08g35600 | A08 | 22610483 | G | A | upstream_gene_variant | MODIFIER | c.-180G>A| |
S77 S82 |
| 7 | BAA08g35600 | A08 | 22611260 | C | T | synonymous_variant | LOW | c.432C>T|p.Val144Val |
S161 |
| 8 | BAA08g35600 | A08 | 22611364 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.457-1G>A| |
S107 |
| 9 | BAA08g35600 | A08 | 22611398 | G | A | missense_variant | MODERATE | c.490G>A|p.Asp164Asn |
S212 |