| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA08g16600 | A08 | 13727111 | G | A | upstream_gene_variant | MODIFIER | c.-3009G>A| |
S174 S39 |
| 2 | BAA08g16600 | A08 | 13727738 | C | T | upstream_gene_variant | MODIFIER | c.-2382C>T| |
S134 |
| 3 | BAA08g16600 | A08 | 13729740 | C | T | upstream_gene_variant | MODIFIER | c.-380C>T| |
S44 |
| 4 | BAA08g16600 | A08 | 13729749 | G | A | upstream_gene_variant | MODIFIER | c.-371G>A| |
S97 |
| 5 | BAA08g16600 | A08 | 13731898 | C | T | synonymous_variant | LOW | c.1030C>T|p.Leu344Leu |
S173 |
| 6 | BAA08g16600 | A08 | 13731934 | G | A | missense_variant | MODERATE | c.1066G>A|p.Ala356Thr |
S281 |
| 7 | BAA08g16600 | A08 | 13732604 | G | A | missense_variant | MODERATE | c.1432G>A|p.Gly478Ser |
S219 S72 |
| 8 | BAA08g16600 | A08 | 13732802 | C | T | synonymous_variant | LOW | c.1542C>T|p.Phe514Phe |
S135 |
| 9 | BAA08g16600 | A08 | 13732925 | C | T | splice_region_variant&intron_variant | LOW | c.1582-8C>T| |
S296 |
| 10 | BAA08g16600 | A08 | 13734326 | G | T | downstream_gene_variant | MODIFIER | c.*592G>T| |
S14 S234 S265 S80 |
| 11 | BAA08g16600 | A08 | 13735482 | C | T | downstream_gene_variant | MODIFIER | c.*1748C>T| |
S213 |