| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g14580 | A01 | 6927770 | C | T | missense_variant | MODERATE | c.859G>A|p.Asp287Asn |
S151 S263 |
| 2 | BAA01g14580 | A01 | 6928058 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.709-1G>A| |
S151 S263 |
| 3 | BAA01g14580 | A01 | 6928360 | C | T | missense_variant | MODERATE | c.616G>A|p.Ala206Thr |
S179 |
| 4 | BAA01g14580 | A01 | 6930041 | G | A | upstream_gene_variant | MODIFIER | c.-648C>T| |
S126 |
| 5 | BAA01g14580 | A01 | 6931651 | G | A | upstream_gene_variant | MODIFIER | c.-2258C>T| |
S297 |
| 6 | BAA01g14580 | A01 | 6931691 | C | T | upstream_gene_variant | MODIFIER | c.-2298G>A| |
S46 |
| 7 | BAA01g14580 | A01 | 6931892 | C | T | upstream_gene_variant | MODIFIER | c.-2499G>A| |
S208 S93 |
| 8 | BAA01g14580 | A01 | 6932206 | C | T | upstream_gene_variant | MODIFIER | c.-2813G>A| |
S46 |
| 9 | BAA01g14580 | A01 | 6932265 | G | A | upstream_gene_variant | MODIFIER | c.-2872C>T| |
S229 |
| 10 | BAA01g14580 | A01 | 6932697 | G | A | upstream_gene_variant | MODIFIER | c.-3304C>T| |
S15 S156 S2 S213 S3 S4 S6 |