| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g35630 | A09 | 44023233 | C | T | upstream_gene_variant | MODIFIER | c.-4798C>T| |
S296 |
| 2 | BAA09g35630 | A09 | 44023980 | C | T | upstream_gene_variant | MODIFIER | c.-4051C>T| |
S132 S137 S138 S237 S288 |
| 3 | BAA09g35630 | A09 | 44024689 | T | G | upstream_gene_variant | MODIFIER | c.-3342T>G| |
S137 S138 S237 S288 |
| 4 | BAA09g35630 | A09 | 44025913 | C | T | upstream_gene_variant | MODIFIER | c.-2118C>T| |
S36 |
| 5 | BAA09g35630 | A09 | 44025984 | C | T | upstream_gene_variant | MODIFIER | c.-2047C>T| |
S259 |
| 6 | BAA09g35630 | A09 | 44027522 | C | T | upstream_gene_variant | MODIFIER | c.-509C>T| |
S240 |
| 7 | BAA09g35630 | A09 | 44027539 | C | T | upstream_gene_variant | MODIFIER | c.-492C>T| |
S156 |
| 8 | BAA09g35630 | A09 | 44028116 | G | A | missense_variant | MODERATE | c.86G>A|p.Gly29Glu |
S112 |
| 9 | BAA09g35630 | A09 | 44029048 | G | A | splice_donor_variant&intron_variant | HIGH | c.474+1G>A| |
S221 |
| 10 | BAA09g35630 | A09 | 44029492 | G | A | splice_region_variant&intron_variant | LOW | c.687+5G>A| |
S172 S217 |
| 11 | BAA09g35630 | A09 | 44030516 | G | A | synonymous_variant | LOW | c.1017G>A|p.Glu339Glu |
S76 |