| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 160551 | BAA02g07750 | A02 | 3334120 | G | A | upstream_gene_variant | MODIFIER | c.-2425C>T| |
S276 |
| 160552 | BAA02g07750 | A02 | 3334126 | G | A | upstream_gene_variant | MODIFIER | c.-2431C>T| |
S165 |
| 160553 | BAA02g07750 | A02 | 3334605 | C | T | upstream_gene_variant | MODIFIER | c.-2910G>A| |
S138 |
| 160554 | BAA02g07750 | A02 | 3335832 | G | A | upstream_gene_variant | MODIFIER | c.-4137C>T| |
S144 |
| 160555 | BAA02g07770 | A02 | 3340569 | G | A | downstream_gene_variant | MODIFIER | c.*4237C>T| |
S158 |
| 160556 | BAA02g07770 | A02 | 3341192 | G | A | downstream_gene_variant | MODIFIER | c.*3614C>T| |
S105 S106 |
| 160557 | BAA02g07760 | A02 | 3343121 | G | A | downstream_gene_variant | MODIFIER | c.*1411G>A| |
S265 |
| 160558 | BAA02g07780 | A02 | 3343689 | C | T | upstream_gene_variant | MODIFIER | c.-4878C>T| |
S33 |
| 160559 | BAA02g07770 | A02 | 3344988 | C | T | missense_variant | MODERATE | c.661G>A|p.Val221Ile |
S295 |
| 160560 | BAA02g07770 | A02 | 3345790 | G | A | missense_variant | MODERATE | c.128C>T|p.Ser43Phe |
S161 |
| 160561 | BAA02g07770 | A02 | 3346719 | C | T | upstream_gene_variant | MODIFIER | c.-802G>A| |
S81 |
| 160562 | BAA02g07770 | A02 | 3346866 | C | T | upstream_gene_variant | MODIFIER | c.-949G>A| |
S229 |
| 160563 | BAA02g07770 | A02 | 3347589 | C | T | upstream_gene_variant | MODIFIER | c.-1672G>A| |
S233 |
| 160564 | BAA02g07770 | A02 | 3347909 | C | T | upstream_gene_variant | MODIFIER | c.-1992G>A| |
S116 S229 |
| 160565 | BAA02g07780 | A02 | 3348751 | C | T | missense_variant&splice_region_variant | MODERATE | c.185C>T|p.Ser62Phe |
S8 |
| 160566 | BAA02g07780 | A02 | 3348979 | G | A | missense_variant | MODERATE | c.242G>A|p.Gly81Asp |
S57 |
| 160567 | BAA02g07770 | A02 | 3349021 | C | T | upstream_gene_variant | MODIFIER | c.-3104G>A| |
S8 |
| 160568 | BAA02g07770 | A02 | 3349120 | G | A | upstream_gene_variant | MODIFIER | c.-3203C>T| |
S163 |
| 160569 | BAA02g07770 | A02 | 3349202 | G | A | upstream_gene_variant | MODIFIER | c.-3285C>T| |
S127 |
| 160570 | BAA02g07770 | A02 | 3349346 | C | T | upstream_gene_variant | MODIFIER | c.-3429G>A| |
S287 |
| 160571 | BAA02g07770 | A02 | 3349930 | C | T | upstream_gene_variant | MODIFIER | c.-4013G>A| |
S9 |
| 160572 | BAA02g07780 | A02 | 3350601 | G | A | missense_variant | MODERATE | c.478G>A|p.Ala160Thr |
S126 |
| 160573 | BAA02g07770 | A02 | 3350678 | C | T | upstream_gene_variant | MODIFIER | c.-4761G>A| |
S216 |
| 160574 | BAA02g07770 | A02 | 3350782 | C | T | upstream_gene_variant | MODIFIER | c.-4865G>A| |
S245 |
| 160575 | BAA02g07780 | A02 | 3353055 | C | T | downstream_gene_variant | MODIFIER | c.*2422C>T| |
S243 |