| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA05g00660 | A05 | 372443 | C | T | missense_variant | MODERATE | c.1265G>A|p.Gly422Glu |
S195 |
| 2 | BAA05g00660 | A05 | 372591 | C | T | missense_variant | MODERATE | c.1201G>A|p.Glu401Lys |
S308 |
| 3 | BAA05g00660 | A05 | 373596 | G | A | missense_variant | MODERATE | c.704C>T|p.Pro235Leu |
S266 |
| 4 | BAA05g00660 | A05 | 373834 | C | T | intron_variant | MODIFIER | c.618+137G>A| |
S257 |
| 5 | BAA05g00660 | A05 | 374066 | C | T | missense_variant | MODERATE | c.523G>A|p.Ala175Thr |
S87 |
| 6 | BAA05g00660 | A05 | 375077 | C | T | missense_variant | MODERATE | c.118G>A|p.Asp40Asn |
S293 |
| 7 | BAA05g00660 | A05 | 375716 | C | T | upstream_gene_variant | MODIFIER | c.-522G>A| |
S201 |
| 8 | BAA05g00660 | A05 | 375797 | C | T | upstream_gene_variant | MODIFIER | c.-603G>A| |
S188 |
| 9 | BAA05g00660 | A05 | 376313 | G | A | upstream_gene_variant | MODIFIER | c.-1119C>T| |
S224 |
| 10 | BAA05g00660 | A05 | 376415 | G | A | upstream_gene_variant | MODIFIER | c.-1221C>T| |
S165 |
| 11 | BAA05g00660 | A05 | 376463 | C | T | upstream_gene_variant | MODIFIER | c.-1269G>A| |
S38 |
| 12 | BAA05g00660 | A05 | 378032 | G | A | upstream_gene_variant | MODIFIER | c.-2838C>T| |
S293 |
| 13 | BAA05g00660 | A05 | 379065 | G | A | upstream_gene_variant | MODIFIER | c.-3871C>T| |
S138 |
| 14 | BAA05g00660 | A05 | 379194 | G | A | upstream_gene_variant | MODIFIER | c.-4000C>T| |
S105 S106 |
| 15 | BAA05g00660 | A05 | 379360 | C | T | upstream_gene_variant | MODIFIER | c.-4166G>A| |
S13 S140 S168 |
| 16 | BAA05g00660 | A05 | 379679 | C | T | upstream_gene_variant | MODIFIER | c.-4485G>A| |
S61 |