| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA05g16060 | A05 | 8827283 | C | T | downstream_gene_variant | MODIFIER | c.*3328G>A| |
S111 |
| 2 | BAA05g16060 | A05 | 8827340 | C | T | downstream_gene_variant | MODIFIER | c.*3271G>A| |
S12 |
| 3 | BAA05g16060 | A05 | 8831339 | C | T | missense_variant | MODERATE | c.2686G>A|p.Asp896Asn |
S211 S227 |
| 4 | BAA05g16060 | A05 | 8831552 | C | T | missense_variant | MODERATE | c.2541G>A|p.Met847Ile |
S126 |
| 5 | BAA05g16060 | A05 | 8832653 | G | A | synonymous_variant | LOW | c.2046C>T|p.Tyr682Tyr |
S78 |
| 6 | BAA05g16060 | A05 | 8832872 | G | A | splice_region_variant&synonymous_variant | LOW | c.1941C>T|p.Phe647Phe |
S54 |
| 7 | BAA05g16060 | A05 | 8833049 | G | A | missense_variant | MODERATE | c.1853C>T|p.Pro618Leu |
S289 |
| 8 | BAA05g16060 | A05 | 8835113 | C | T | missense_variant | MODERATE | c.413G>A|p.Ser138Asn |
S5 |
| 9 | BAA05g16060 | A05 | 8835919 | G | A | upstream_gene_variant | MODIFIER | c.-86C>T| |
S260 |
| 10 | BAA05g16060 | A05 | 8836442 | C | T | upstream_gene_variant | MODIFIER | c.-609G>A| |
S265 |
| 11 | BAA05g16060 | A05 | 8837119 | C | T | upstream_gene_variant | MODIFIER | c.-1286G>A| |
S114 |
| 12 | BAA05g16060 | A05 | 8837734 | G | A | upstream_gene_variant | MODIFIER | c.-1901C>T| |
S150 |
| 13 | BAA05g16060 | A05 | 8837893 | C | T | upstream_gene_variant | MODIFIER | c.-2060G>A| |
S9 |
| 14 | BAA05g16060 | A05 | 8838026 | C | T | upstream_gene_variant | MODIFIER | c.-2193G>A| |
S46 |
| 15 | BAA05g16060 | A05 | 8838156 | C | T | upstream_gene_variant | MODIFIER | c.-2323G>A| |
S57 |
| 16 | BAA05g16060 | A05 | 8838283 | G | A | upstream_gene_variant | MODIFIER | c.-2450C>T| |
S132 S137 |
| 17 | BAA05g16060 | A05 | 8838562 | G | A | upstream_gene_variant | MODIFIER | c.-2729C>T| |
S303 |
| 18 | BAA05g16060 | A05 | 8838759 | G | A | upstream_gene_variant | MODIFIER | c.-2926C>T| |
S144 |
| 19 | BAA05g16060 | A05 | 8838854 | C | T | upstream_gene_variant | MODIFIER | c.-3021G>A| |
S188 |