| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g34840 | A09 | 43261203 | C | T | upstream_gene_variant | MODIFIER | c.-4546C>T| |
S183 S198 |
| 2 | BAA09g34840 | A09 | 43263611 | G | A | upstream_gene_variant | MODIFIER | c.-2138G>A| |
S166 |
| 3 | BAA09g34840 | A09 | 43263829 | C | T | upstream_gene_variant | MODIFIER | c.-1920C>T| |
S83 S88 |
| 4 | BAA09g34840 | A09 | 43263912 | G | A | upstream_gene_variant | MODIFIER | c.-1837G>A| |
S12 |
| 5 | BAA09g34840 | A09 | 43265932 | C | T | missense_variant | MODERATE | c.184C>T|p.Pro62Ser |
S273 |
| 6 | BAA09g34840 | A09 | 43266532 | C | T | intron_variant | MODIFIER | c.768+16C>T| |
S211 S227 |
| 7 | BAA09g34840 | A09 | 43267263 | G | A | missense_variant | MODERATE | c.1153G>A|p.Gly385Ser |
S170 |
| 8 | BAA09g34840 | A09 | 43267665 | G | A | downstream_gene_variant | MODIFIER | c.*391G>A| |
S142 |
| 9 | BAA09g34840 | A09 | 43267721 | C | T | downstream_gene_variant | MODIFIER | c.*447C>T| |
S152 |
| 10 | BAA09g34840 | A09 | 43271598 | C | T | downstream_gene_variant | MODIFIER | c.*4324C>T| |
S277 |