| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 154351 | BAA02g02640 | A02 | 1199697 | G | A | missense_variant | MODERATE | c.3941C>T|p.Ser1314Leu |
S188 |
| 154352 | BAA02g02640 | A02 | 1200056 | G | A | missense_variant | MODERATE | c.3667C>T|p.Pro1223Ser |
S264 |
| 154353 | BAA02g02640 | A02 | 1201070 | G | A | missense_variant | MODERATE | c.2653C>T|p.Pro885Ser |
S274 |
| 154354 | BAA02g02640 | A02 | 1201217 | G | A | missense_variant | MODERATE | c.2506C>T|p.Pro836Ser |
S81 S85 |
| 154355 | BAA02g02640 | A02 | 1201289 | G | A | missense_variant | MODERATE | c.2434C>T|p.Pro812Ser |
S61 S98 |
| 154356 | BAA02g02640 | A02 | 1201658 | G | A | missense_variant | MODERATE | c.2065C>T|p.Pro689Ser |
S60 |
| 154357 | BAA02g02640 | A02 | 1202062 | G | A | missense_variant | MODERATE | c.1661C>T|p.Ser554Phe |
S48 |
| 154358 | BAA02g02640 | A02 | 1202161 | C | T | missense_variant | MODERATE | c.1562G>A|p.Gly521Glu |
S272 |
| 154359 | BAA02g02640 | A02 | 1202579 | G | A | missense_variant | MODERATE | c.1144C>T|p.His382Tyr |
S303 |
| 154360 | BAA02g02650 | A02 | 1203167 | C | T | downstream_gene_variant | MODIFIER | c.*3267G>A| |
S245 |
| 154361 | BAA02g02650 | A02 | 1203177 | C | T | downstream_gene_variant | MODIFIER | c.*3257G>A| |
S61 |
| 154362 | BAA02g02640 | A02 | 1203819 | G | A | synonymous_variant | LOW | c.390C>T|p.Gly130Gly |
S165 |
| 154363 | BAA02g02650 | A02 | 1204299 | G | A | downstream_gene_variant | MODIFIER | c.*2135C>T| |
S168 |
| 154364 | BAA02g02650 | A02 | 1204345 | C | T | downstream_gene_variant | MODIFIER | c.*2089G>A| |
S100 |
| 154365 | BAA02g02650 | A02 | 1204459 | G | A | downstream_gene_variant | MODIFIER | c.*1975C>T| |
S292 |
| 154366 | BAA02g02650 | A02 | 1206559 | G | A | synonymous_variant | LOW | c.1255C>T|p.Leu419Leu |
S206 S26 |
| 154367 | BAA02g02650 | A02 | 1206582 | G | A | missense_variant | MODERATE | c.1232C>T|p.Pro411Leu |
S276 |
| 154368 | BAA02g02650 | A02 | 1207013 | G | A | missense_variant | MODERATE | c.977C>T|p.Pro326Leu |
S131 |
| 154369 | BAA02g02640 | A02 | 1207201 | C | T | upstream_gene_variant | MODIFIER | c.-2438G>A| |
S219 |
| 154370 | BAA02g02640 | A02 | 1207230 | G | A | upstream_gene_variant | MODIFIER | c.-2467C>T| |
S171 |
| 154371 | BAA02g02650 | A02 | 1207992 | G | A | missense_variant | MODERATE | c.782C>T|p.Pro261Leu |
S204 |
| 154372 | BAA02g02650 | A02 | 1208022 | G | A | missense_variant | MODERATE | c.752C>T|p.Ser251Phe |
S308 |
| 154373 | BAA02g02650 | A02 | 1208520 | C | T | missense_variant | MODERATE | c.439G>A|p.Asp147Asn |
S13 |
| 154374 | BAA02g02640 | A02 | 1208982 | G | A | upstream_gene_variant | MODIFIER | c.-4219C>T| |
S57 |
| 154375 | BAA02g02650 | A02 | 1210027 | C | T | upstream_gene_variant | MODIFIER | c.-1069G>A| |
S251 |