| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g18120 | A09 | 10864846 | C | T | upstream_gene_variant | MODIFIER | c.-3821C>T| |
S67 |
| 2 | BAA09g18120 | A09 | 10867836 | C | T | upstream_gene_variant | MODIFIER | c.-831C>T| |
S41 |
| 3 | BAA09g18120 | A09 | 10867862 | G | A | upstream_gene_variant | MODIFIER | c.-805G>A| |
S23 |
| 4 | BAA09g18120 | A09 | 10868007 | G | A | upstream_gene_variant | MODIFIER | c.-660G>A| |
S130 |
| 5 | BAA09g18120 | A09 | 10868249 | G | A | upstream_gene_variant | MODIFIER | c.-418G>A| |
S267 |
| 6 | BAA09g18120 | A09 | 10868535 | C | T | upstream_gene_variant | MODIFIER | c.-132C>T| |
S303 |
| 7 | BAA09g18120 | A09 | 10869110 | G | A | splice_region_variant&synonymous_variant | LOW | c.150G>A|p.Gly50Gly |
S121 |
| 8 | BAA09g18120 | A09 | 10869180 | G | A | splice_donor_variant&intron_variant | HIGH | c.219+1G>A| |
S308 |
| 9 | BAA09g18120 | A09 | 10869526 | G | A | missense_variant | MODERATE | c.385G>A|p.Asp129Asn |
S240 |