| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA10g17770 | A10 | 16959453 | C | T | downstream_gene_variant | MODIFIER | c.*3163G>A| |
S83 S88 |
| 2 | BAA10g17770 | A10 | 16961501 | G | A | downstream_gene_variant | MODIFIER | c.*1115C>T| |
S203 |
| 3 | BAA10g17770 | A10 | 16962635 | G | A | missense_variant | MODERATE | c.1091C>T|p.Thr364Ile |
S3 |
| 4 | BAA10g17770 | A10 | 16963012 | C | T | missense_variant | MODERATE | c.799G>A|p.Val267Ile |
S283 |
| 5 | BAA10g17770 | A10 | 16963280 | G | A | synonymous_variant | LOW | c.531C>T|p.Ile177Ile |
S195 |
| 6 | BAA10g17770 | A10 | 16963693 | G | A | synonymous_variant | LOW | c.237C>T|p.Leu79Leu |
S286 |
| 7 | BAA10g17770 | A10 | 16964367 | C | T | upstream_gene_variant | MODIFIER | c.-124G>A| |
S130 |
| 8 | BAA10g17770 | A10 | 16964660 | C | T | upstream_gene_variant | MODIFIER | c.-417G>A| |
S50 |
| 9 | BAA10g17770 | A10 | 16965043 | C | T | upstream_gene_variant | MODIFIER | c.-800G>A| |
S103 |
| 10 | BAA10g17770 | A10 | 16965599 | C | T | upstream_gene_variant | MODIFIER | c.-1356G>A| |
S188 |
| 11 | BAA10g17770 | A10 | 16965614 | C | T | upstream_gene_variant | MODIFIER | c.-1371G>A| |
S23 |
| 12 | BAA10g17770 | A10 | 16965750 | G | A | upstream_gene_variant | MODIFIER | c.-1507C>T| |
S105 S106 |
| 13 | BAA10g17770 | A10 | 16967459 | C | T | upstream_gene_variant | MODIFIER | c.-3216G>A| |
S170 |
| 14 | BAA10g17770 | A10 | 16967490 | G | A | upstream_gene_variant | MODIFIER | c.-3247C>T| |
S53 |