| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 158251 | BAA02g05900 | A02 | 2509183 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.281-1G>A| |
S33 |
| 158252 | BAA02g05880 | A02 | 2509410 | G | A | upstream_gene_variant | MODIFIER | c.-4224C>T| |
S297 |
| 158253 | BAA02g05880 | A02 | 2509668 | G | A | upstream_gene_variant | MODIFIER | c.-4482C>T| |
|
| 158254 | BAA02g05880 | A02 | 2509690 | G | A | upstream_gene_variant | MODIFIER | c.-4504C>T| |
S295 |
| 158255 | BAA02g05880 | A02 | 2509880 | A | G | upstream_gene_variant | MODIFIER | c.-4694T>C| |
S301 S304 |
| 158256 | BAA02g05890 | A02 | 2511103 | G | A | upstream_gene_variant | MODIFIER | c.-4994C>T| |
S136 |
| 158257 | BAA02g05910 | A02 | 2512061 | C | T | missense_variant | MODERATE | c.1381G>A|p.Gly461Ser |
S116 |
| 158258 | BAA02g05910 | A02 | 2512112 | G | A | synonymous_variant | LOW | c.1330C>T|p.Leu444Leu |
S132 S137 S215 |
| 158259 | BAA02g05910 | A02 | 2512160 | C | T | missense_variant | MODERATE | c.1282G>A|p.Gly428Arg |
S117 |
| 158260 | BAA02g05910 | A02 | 2512243 | G | A | missense_variant | MODERATE | c.1199C>T|p.Ser400Phe |
S132 S89 |
| 158261 | BAA02g05910 | A02 | 2512380 | G | A | synonymous_variant | LOW | c.1062C>T|p.Tyr354Tyr |
S7 |
| 158262 | BAA02g05910 | A02 | 2512656 | C | T | synonymous_variant | LOW | c.786G>A|p.Gln262Gln |
S185 |
| 158263 | BAA02g05910 | A02 | 2512724 | G | A | missense_variant | MODERATE | c.718C>T|p.Pro240Ser |
S266 |
| 158264 | BAA02g05900 | A02 | 2512967 | C | T | upstream_gene_variant | MODIFIER | c.-3197G>A| |
S152 |
| 158265 | BAA02g05910 | A02 | 2513212 | C | T | missense_variant | MODERATE | c.490G>A|p.Val164Ile |
S233 |
| 158266 | BAA02g05910 | A02 | 2513405 | G | A | synonymous_variant | LOW | c.297C>T|p.Asp99Asp |
S118 |
| 158267 | BAA02g05900 | A02 | 2513488 | C | T | upstream_gene_variant | MODIFIER | c.-3718G>A| |
S240 |
| 158268 | BAA02g05910 | A02 | 2513830 | C | T | synonymous_variant | LOW | c.60G>A|p.Ser20Ser |
S63 |
| 158269 | BAA02g05920 | A02 | 2515299 | C | T | missense_variant | MODERATE | c.997G>A|p.Gly333Arg |
S292 |
| 158270 | BAA02g05920 | A02 | 2516194 | G | A | synonymous_variant | LOW | c.102C>T|p.Leu34Leu |
S143 |
| 158271 | BAA02g05910 | A02 | 2516327 | C | T | upstream_gene_variant | MODIFIER | c.-2438G>A| |
S241 |
| 158272 | BAA02g05910 | A02 | 2516671 | C | T | upstream_gene_variant | MODIFIER | c.-2782G>A| |
S202 |
| 158273 | BAA02g05910 | A02 | 2518851 | C | T | upstream_gene_variant | MODIFIER | c.-4962G>A| |
S87 |
| 158274 | BAA02g05920 | A02 | 2519974 | G | A | upstream_gene_variant | MODIFIER | c.-3679C>T| |
S136 |
| 158275 | BAA02g05940 | A02 | 2520494 | G | A | synonymous_variant | LOW | c.216G>A|p.Lys72Lys |
S190 |