| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 10851 | BAA01g08720 | A01 | 3856138 | C | T | downstream_gene_variant | MODIFIER | c.*3667C>T| |
S164 |
| 10852 | BAA01g08720 | A01 | 3856503 | C | T | downstream_gene_variant | MODIFIER | c.*4032C>T| |
S148 S30 S31 |
| 10853 | BAA01g08720 | A01 | 3856570 | C | T | downstream_gene_variant | MODIFIER | c.*4099C>T| |
S16 |
| 10854 | BAA01g08730 | A01 | 3857709 | C | T | upstream_gene_variant | MODIFIER | c.-4355C>T| |
S246 |
| 10855 | BAA01g08730 | A01 | 3858549 | G | A | upstream_gene_variant | MODIFIER | c.-3515G>A| |
S216 |
| 10856 | BAA01g08730 | A01 | 3858580 | G | A | upstream_gene_variant | MODIFIER | c.-3484G>A| |
S105 S106 |
| 10857 | BAA01g08740 | A01 | 3863893 | G | A | upstream_gene_variant | MODIFIER | c.-108C>T| |
S202 |
| 10858 | BAA01g08740 | A01 | 3865532 | C | T | upstream_gene_variant | MODIFIER | c.-1747G>A| |
S255 |
| 10859 | BAA01g08740 | A01 | 3866332 | G | A | upstream_gene_variant | MODIFIER | c.-2547C>T| |
S302 |
| 10860 | BAA01g08750 | A01 | 3867029 | C | T | synonymous_variant | LOW | c.435C>T|p.Asn145Asn |
S112 |
| 10861 | BAA01g08750 | A01 | 3867059 | G | A | stop_gained | HIGH | c.465G>A|p.Trp155* |
S207 |
| 10862 | BAA01g08750 | A01 | 3867255 | G | A | missense_variant | MODERATE | c.661G>A|p.Asp221Asn |
S86 |
| 10863 | BAA01g08740 | A01 | 3868712 | C | T | upstream_gene_variant | MODIFIER | c.-4927G>A| |
S260 |
| 10864 | BAA01g08760 | A01 | 3869836 | C | T | missense_variant | MODERATE | c.686C>T|p.Pro229Leu |
S260 |
| 10865 | BAA01g08760 | A01 | 3869854 | C | T | missense_variant | MODERATE | c.704C>T|p.Thr235Ile |
S205 |
| 10866 | BAA01g08760 | A01 | 3870432 | G | A | missense_variant | MODERATE | c.1282G>A|p.Ala428Thr |
S33 |
| 10867 | BAA01g08760 | A01 | 3870472 | C | T | missense_variant | MODERATE | c.1322C>T|p.Ser441Phe |
S282 |
| 10868 | BAA01g08770 | A01 | 3870673 | G | A | upstream_gene_variant | MODIFIER | c.-2674G>A| |
S137 S138 S237 |
| 10869 | BAA01g08770 | A01 | 3870842 | C | T | upstream_gene_variant | MODIFIER | c.-2505C>T| |
S200 |
| 10870 | BAA01g08770 | A01 | 3871690 | C | T | upstream_gene_variant | MODIFIER | c.-1657C>T| |
S125 |
| 10871 | BAA01g08770 | A01 | 3871764 | C | T | upstream_gene_variant | MODIFIER | c.-1583C>T| |
S266 |
| 10872 | BAA01g08770 | A01 | 3872223 | G | A | upstream_gene_variant | MODIFIER | c.-1124G>A| |
S14 |
| 10873 | BAA01g08770 | A01 | 3872465 | C | T | upstream_gene_variant | MODIFIER | c.-882C>T| |
S81 S85 |
| 10874 | BAA01g08770 | A01 | 3872546 | C | T | upstream_gene_variant | MODIFIER | c.-801C>T| |
S282 |
| 10875 | BAA01g08770 | A01 | 3872710 | C | T | upstream_gene_variant | MODIFIER | c.-637C>T| |
S182 |