| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g15630 | A09 | 8969634 | G | A | upstream_gene_variant | MODIFIER | c.-4104G>A| |
S178 |
| 2 | BAA09g15630 | A09 | 8970789 | C | T | upstream_gene_variant | MODIFIER | c.-2949C>T| |
S296 |
| 3 | BAA09g15630 | A09 | 8971367 | G | A | upstream_gene_variant | MODIFIER | c.-2371G>A| |
S252 |
| 4 | BAA09g15630 | A09 | 8973090 | G | A | upstream_gene_variant | MODIFIER | c.-648G>A| |
S288 |
| 5 | BAA09g15630 | A09 | 8973706 | C | T | upstream_gene_variant | MODIFIER | c.-32C>T| |
S75 S81 |
| 6 | BAA09g15630 | A09 | 8973964 | C | T | missense_variant | MODERATE | c.227C>T|p.Ser76Phe |
S134 |
| 7 | BAA09g15630 | A09 | 8973968 | G | A | synonymous_variant | LOW | c.231G>A|p.Lys77Lys |
S38 |
| 8 | BAA09g15630 | A09 | 8975372 | C | T | missense_variant | MODERATE | c.1321C>T|p.Leu441Phe |
S59 |
| 9 | BAA09g15630 | A09 | 8978325 | C | T | downstream_gene_variant | MODIFIER | c.*2425C>T| |
S62 |
| 10 | BAA09g15630 | A09 | 8978687 | G | A | downstream_gene_variant | MODIFIER | c.*2787G>A| |
S12 |
| 11 | BAA09g15630 | A09 | 8979226 | C | T | downstream_gene_variant | MODIFIER | c.*3326C>T| |
S186 |
| 12 | BAA09g15630 | A09 | 8979897 | C | T | downstream_gene_variant | MODIFIER | c.*3997C>T| |
S288 |
| 13 | BAA09g15630 | A09 | 8979969 | C | T | downstream_gene_variant | MODIFIER | c.*4069C>T| |
S43 |
| 14 | BAA09g15630 | A09 | 8980597 | G | A | downstream_gene_variant | MODIFIER | c.*4697G>A| |
S192 |