| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA08g05810 | A08 | 4477342 | G | A | upstream_gene_variant | MODIFIER | c.-4919G>A| |
S32 |
| 2 | BAA08g05810 | A08 | 4479976 | C | T | upstream_gene_variant | MODIFIER | c.-2285C>T| |
S132 S137 |
| 3 | BAA08g05810 | A08 | 4480173 | G | A | upstream_gene_variant | MODIFIER | c.-2088G>A| |
S122 |
| 4 | BAA08g05810 | A08 | 4481279 | C | T | upstream_gene_variant | MODIFIER | c.-982C>T| |
S148 S30 S31 |
| 5 | BAA08g05810 | A08 | 4481608 | T | G | upstream_gene_variant | MODIFIER | c.-653T>G| |
S260 |
| 6 | BAA08g05810 | A08 | 4482285 | G | A | missense_variant | MODERATE | c.25G>A|p.Glu9Lys |
S158 |
| 7 | BAA08g05810 | A08 | 4483141 | C | T | intron_variant | MODIFIER | c.257+528C>T| |
S134 |
| 8 | BAA08g05810 | A08 | 4483361 | G | A | intron_variant | MODIFIER | c.258-481G>A| |
S222 S227 S258 |
| 9 | BAA08g05810 | A08 | 4483852 | G | A | missense_variant | MODERATE | c.268G>A|p.Asp90Asn |
S238 |
| 10 | BAA08g05810 | A08 | 4484106 | G | A | intron_variant | MODIFIER | c.375-62G>A| |
S278 |
| 11 | BAA08g05810 | A08 | 4485732 | C | T | downstream_gene_variant | MODIFIER | c.*479C>T| |
S281 |
| 12 | BAA08g05810 | A08 | 4485876 | C | T | downstream_gene_variant | MODIFIER | c.*623C>T| |
S43 |
| 13 | BAA08g05810 | A08 | 4485980 | G | A | downstream_gene_variant | MODIFIER | c.*727G>A| |
S115 |
| 14 | BAA08g05810 | A08 | 4486015 | C | G | downstream_gene_variant | MODIFIER | c.*762C>G| |
S116 |
| 15 | BAA08g05810 | A08 | 4486045 | C | T | downstream_gene_variant | MODIFIER | c.*792C>T| |
S170 |
| 16 | BAA08g05810 | A08 | 4486257 | C | T | downstream_gene_variant | MODIFIER | c.*1004C>T| |
S156 |
| 17 | BAA08g05810 | A08 | 4486508 | G | A | downstream_gene_variant | MODIFIER | c.*1255G>A| |
S199 |