| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA07g08430 | A07 | 17484101 | G | A | downstream_gene_variant | MODIFIER | c.*4896C>T| |
S46 |
| 2 | BAA07g08430 | A07 | 17484107 | G | A | downstream_gene_variant | MODIFIER | c.*4890C>T| |
S65 |
| 3 | BAA07g08430 | A07 | 17484835 | C | T | downstream_gene_variant | MODIFIER | c.*4162G>A| |
S153 |
| 4 | BAA07g08430 | A07 | 17487828 | G | A | downstream_gene_variant | MODIFIER | c.*1169C>T| |
S158 |
| 5 | BAA07g08430 | A07 | 17489293 | G | A | missense_variant | MODERATE | c.25C>T|p.Leu9Phe |
S219 |
| 6 | BAA07g08430 | A07 | 17489789 | G | A | upstream_gene_variant | MODIFIER | c.-472C>T| |
S40 S49 |
| 7 | BAA07g08430 | A07 | 17489925 | G | A | upstream_gene_variant | MODIFIER | c.-608C>T| |
S237 |
| 8 | BAA07g08430 | A07 | 17489975 | C | T | upstream_gene_variant | MODIFIER | c.-658G>A| |
S289 S290 |
| 9 | BAA07g08430 | A07 | 17490241 | G | A | upstream_gene_variant | MODIFIER | c.-924C>T| |
S132 S137 S215 |
| 10 | BAA07g08430 | A07 | 17490443 | G | A | upstream_gene_variant | MODIFIER | c.-1126C>T| |
S139 |
| 11 | BAA07g08430 | A07 | 17490458 | T | C | upstream_gene_variant | MODIFIER | c.-1141A>G| |
S106 |
| 12 | BAA07g08430 | A07 | 17490537 | C | T | upstream_gene_variant | MODIFIER | c.-1220G>A| |
S303 |
| 13 | BAA07g08430 | A07 | 17490814 | G | A | upstream_gene_variant | MODIFIER | c.-1497C>T| |
S65 |
| 14 | BAA07g08430 | A07 | 17491540 | G | A | upstream_gene_variant | MODIFIER | c.-2223C>T| |
S251 |
| 15 | BAA07g08430 | A07 | 17492210 | C | T | upstream_gene_variant | MODIFIER | c.-2893G>A| |
S216 |
| 16 | BAA07g08430 | A07 | 17492977 | C | A | upstream_gene_variant | MODIFIER | c.-3660G>T| |
S53 |
| 17 | BAA07g08430 | A07 | 17493136 | G | A | upstream_gene_variant | MODIFIER | c.-3819C>T| |
S231 |