| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 154101 | BAA02g02470 | A02 | 1103810 | G | A | missense_variant | MODERATE | c.124G>A|p.Ala42Thr |
S163 |
| 154102 | BAA02g02470 | A02 | 1104251 | C | T | missense_variant | MODERATE | c.449C>T|p.Ala150Val |
S252 |
| 154103 | BAA02g02470 | A02 | 1104275 | G | A | missense_variant | MODERATE | c.473G>A|p.Ser158Asn |
S225 S73 |
| 154104 | BAA02g02470 | A02 | 1104284 | C | T | missense_variant | MODERATE | c.482C>T|p.Thr161Ile |
S81 S85 |
| 154105 | BAA02g02470 | A02 | 1104485 | C | T | missense_variant | MODERATE | c.683C>T|p.Ser228Leu |
S249 |
| 154106 | BAA02g02470 | A02 | 1104493 | G | A | missense_variant | MODERATE | c.691G>A|p.Gly231Ser |
S15 S2 S3 S34 |
| 154107 | BAA02g02470 | A02 | 1105055 | C | T | downstream_gene_variant | MODIFIER | c.*485C>T| |
S221 |
| 154108 | BAA02g02470 | A02 | 1106369 | C | T | downstream_gene_variant | MODIFIER | c.*1799C>T| |
S240 |
| 154109 | BAA02g02470 | A02 | 1107240 | C | T | downstream_gene_variant | MODIFIER | c.*2670C>T| |
S100 |
| 154110 | BAA02g02470 | A02 | 1107880 | C | T | downstream_gene_variant | MODIFIER | c.*3310C>T| |
S37 |
| 154111 | BAA02g02470 | A02 | 1108390 | G | A | downstream_gene_variant | MODIFIER | c.*3820G>A| |
S51 |
| 154112 | BAA02g02480 | A02 | 1112095 | G | A | upstream_gene_variant | MODIFIER | c.-4085G>A| |
S136 |
| 154113 | BAA02g02480 | A02 | 1114604 | G | A | upstream_gene_variant | MODIFIER | c.-1576G>A| |
S302 |
| 154114 | BAA02g02480 | A02 | 1115937 | A | T | upstream_gene_variant | MODIFIER | c.-243A>T| |
S252 |
| 154115 | BAA02g02480 | A02 | 1116081 | C | T | upstream_gene_variant | MODIFIER | c.-99C>T| |
S15 S2 S3 S34 |
| 154116 | BAA02g02480 | A02 | 1116163 | G | A | upstream_gene_variant | MODIFIER | c.-17G>A| |
S177 |
| 154117 | BAA02g02480 | A02 | 1116380 | C | T | synonymous_variant | LOW | c.201C>T|p.Phe67Phe |
S264 |
| 154118 | BAA02g02480 | A02 | 1116402 | G | A | missense_variant | MODERATE | c.223G>A|p.Asp75Asn |
S67 |
| 154119 | BAA02g02480 | A02 | 1117087 | C | T | intron_variant | MODIFIER | c.364+544C>T| |
S38 |
| 154120 | BAA02g02490 | A02 | 1117407 | C | T | downstream_gene_variant | MODIFIER | c.*4791G>A| |
S193 |
| 154121 | BAA02g02480 | A02 | 1118016 | G | A | missense_variant | MODERATE | c.581G>A|p.Arg194Lys |
S5 |
| 154122 | BAA02g02480 | A02 | 1118272 | G | A | synonymous_variant | LOW | c.837G>A|p.Glu279Glu |
S259 |
| 154123 | BAA02g02480 | A02 | 1118868 | G | A | missense_variant | MODERATE | c.1249G>A|p.Glu417Lys |
S293 |
| 154124 | BAA02g02480 | A02 | 1118920 | G | A | missense_variant | MODERATE | c.1301G>A|p.Arg434Lys |
S62 |
| 154125 | BAA02g02480 | A02 | 1119440 | G | A | downstream_gene_variant | MODIFIER | c.*414G>A| |
S163 |