| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 156101 | BAA02g04190 | A02 | 1817025 | C | T | missense_variant | MODERATE | c.844G>A|p.Glu282Lys |
S131 |
| 156102 | BAA02g04190 | A02 | 1817469 | C | T | missense_variant | MODERATE | c.400G>A|p.Asp134Asn |
S272 |
| 156103 | BAA02g04190 | A02 | 1822102 | C | T | upstream_gene_variant | MODIFIER | c.-4234G>A| |
S40 S49 |
| 156104 | BAA02g04190 | A02 | 1822238 | G | A | upstream_gene_variant | MODIFIER | c.-4370C>T| |
S4 |
| 156105 | BAA02g04200 | A02 | 1825081 | C | T | downstream_gene_variant | MODIFIER | c.*3601C>T| |
S95 |
| 156106 | BAA02g04220 | A02 | 1825440 | G | A | upstream_gene_variant | MODIFIER | c.-4877G>A| |
S223 |
| 156107 | BAA02g04220 | A02 | 1829910 | G | A | upstream_gene_variant | MODIFIER | c.-407G>A| |
S288 |
| 156108 | BAA02g04220 | A02 | 1830945 | C | T | missense_variant | MODERATE | c.629C>T|p.Pro210Leu |
S284 |
| 156109 | BAA02g04220 | A02 | 1831144 | G | A | synonymous_variant | LOW | c.828G>A|p.Gly276Gly |
S11 |
| 156110 | BAA02g04220 | A02 | 1831145 | A | T | stop_gained | HIGH | c.829A>T|p.Arg277* |
S236 |
| 156111 | BAA02g04220 | A02 | 1831190 | G | A | missense_variant | MODERATE | c.874G>A|p.Val292Ile |
S189 |
| 156112 | BAA02g04220 | A02 | 1831988 | G | A | downstream_gene_variant | MODIFIER | c.*493G>A| |
S271 |
| 156113 | BAA02g04220 | A02 | 1832702 | G | A | downstream_gene_variant | MODIFIER | c.*1207G>A| |
S205 |
| 156114 | BAA02g04220 | A02 | 1833459 | C | T | downstream_gene_variant | MODIFIER | c.*1964C>T| |
S1 S90 |
| 156115 | BAA02g04220 | A02 | 1834753 | G | A | downstream_gene_variant | MODIFIER | c.*3258G>A| |
S303 |
| 156116 | BAA02g04220 | A02 | 1835712 | G | A | downstream_gene_variant | MODIFIER | c.*4217G>A| |
S52 |
| 156117 | BAA02g04240 | A02 | 1843786 | G | A | downstream_gene_variant | MODIFIER | c.*1586C>T| |
S166 |
| 156118 | BAA02g04230 | A02 | 1844714 | G | A | synonymous_variant | LOW | c.930G>A|p.Glu310Glu |
S163 |
| 156119 | BAA02g04230 | A02 | 1844730 | G | A | missense_variant | MODERATE | c.946G>A|p.Gly316Ser |
S125 |
| 156120 | BAA02g04230 | A02 | 1844978 | G | A | downstream_gene_variant | MODIFIER | c.*93G>A| |
S223 |
| 156121 | BAA02g04230 | A02 | 1845085 | C | T | downstream_gene_variant | MODIFIER | c.*200C>T| |
S40 S49 |
| 156122 | BAA02g04240 | A02 | 1845791 | C | T | synonymous_variant | LOW | c.15G>A|p.Gln5Gln |
S240 |
| 156123 | BAA02g04240 | A02 | 1846888 | C | T | upstream_gene_variant | MODIFIER | c.-1083G>A| |
S201 |
| 156124 | BAA02g04240 | A02 | 1847366 | C | T | upstream_gene_variant | MODIFIER | c.-1561G>A| |
S274 |
| 156125 | BAA02g04240 | A02 | 1848012 | C | T | upstream_gene_variant | MODIFIER | c.-2207G>A| |
S167 S82 S92 |