| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA08g10000 | A08 | 9101450 | G | A | synonymous_variant | LOW | c.1363C>T|p.Leu455Leu |
S246 |
| 2 | BAA08g10000 | A08 | 9101862 | A | G | synonymous_variant | LOW | c.951T>C|p.Asn317Asn |
S162 |
| 3 | BAA08g10000 | A08 | 9102427 | G | A | synonymous_variant | LOW | c.555C>T|p.Leu185Leu |
S125 |
| 4 | BAA08g10000 | A08 | 9102519 | G | A | missense_variant | MODERATE | c.463C>T|p.Pro155Ser |
S65 |
| 5 | BAA08g10000 | A08 | 9104357 | C | T | upstream_gene_variant | MODIFIER | c.-1376G>A| |
S46 |
| 6 | BAA08g10000 | A08 | 9105335 | C | T | upstream_gene_variant | MODIFIER | c.-2354G>A| |
S82 S92 |
| 7 | BAA08g10000 | A08 | 9106504 | G | A | upstream_gene_variant | MODIFIER | c.-3523C>T| |
S245 |
| 8 | BAA08g10000 | A08 | 9107708 | G | A | upstream_gene_variant | MODIFIER | c.-4727C>T| |
S229 |
| 9 | BAA08g10000 | A08 | 9107960 | C | T | upstream_gene_variant | MODIFIER | c.-4979G>A| |
S160 |