| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA07g04000 | A07 | 3285514 | C | T | downstream_gene_variant | MODIFIER | c.*4443G>A| |
S267 |
| 2 | BAA07g04000 | A07 | 3290231 | C | T | synonymous_variant | LOW | c.726G>A|p.Leu242Leu |
S78 |
| 3 | BAA07g04000 | A07 | 3290280 | G | A | missense_variant | MODERATE | c.677C>T|p.Ala226Val |
S166 |
| 4 | BAA07g04000 | A07 | 3290694 | C | T | missense_variant | MODERATE | c.479G>A|p.Arg160Lys |
S86 |
| 5 | BAA07g04000 | A07 | 3291248 | G | A | upstream_gene_variant | MODIFIER | c.-76C>T| |
S199 |
| 6 | BAA07g04000 | A07 | 3291343 | G | A | upstream_gene_variant | MODIFIER | c.-171C>T| |
S216 |
| 7 | BAA07g04000 | A07 | 3291593 | C | T | upstream_gene_variant | MODIFIER | c.-421G>A| |
S218 |
| 8 | BAA07g04000 | A07 | 3291628 | C | T | upstream_gene_variant | MODIFIER | c.-456G>A| |
S100 |
| 9 | BAA07g04000 | A07 | 3291733 | C | T | upstream_gene_variant | MODIFIER | c.-561G>A| |
S4 |
| 10 | BAA07g04000 | A07 | 3293081 | G | A | upstream_gene_variant | MODIFIER | c.-1909C>T| |
S15 S3 |