| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 174701 | BAA02g17490 | A02 | 8714277 | C | T | missense_variant | MODERATE | c.1523C>T|p.Ser508Phe |
S44 |
| 174702 | BAA02g17490 | A02 | 8714773 | C | T | synonymous_variant | LOW | c.2019C>T|p.Ser673Ser |
S71 |
| 174703 | BAA02g17500 | A02 | 8716399 | G | A | upstream_gene_variant | MODIFIER | c.-1013G>A| |
S197 |
| 174704 | BAA02g17500 | A02 | 8716492 | C | T | upstream_gene_variant | MODIFIER | c.-920C>T| |
S121 |
| 174705 | BAA02g17500 | A02 | 8716680 | C | T | upstream_gene_variant | MODIFIER | c.-732C>T| |
S25 |
| 174706 | BAA02g17500 | A02 | 8716716 | C | T | upstream_gene_variant | MODIFIER | c.-696C>T| |
S271 |
| 174707 | BAA02g17500 | A02 | 8717230 | C | T | upstream_gene_variant | MODIFIER | c.-182C>T| |
S308 |
| 174708 | BAA02g17500 | A02 | 8717615 | G | A | synonymous_variant | LOW | c.204G>A|p.Arg68Arg |
S132 S215 |
| 174709 | BAA02g17500 | A02 | 8718264 | C | T | missense_variant | MODERATE | c.787C>T|p.Leu263Phe |
S119 |
| 174710 | BAA02g17500 | A02 | 8718292 | C | T | missense_variant | MODERATE | c.815C>T|p.Ser272Phe |
S242 |
| 174711 | BAA02g17510 | A02 | 8718959 | G | A | upstream_gene_variant | MODIFIER | c.-3348G>A| |
S122 |
| 174712 | BAA02g17500 | A02 | 8719807 | G | A | missense_variant | MODERATE | c.1811G>A|p.Arg604Lys |
S177 |
| 174713 | BAA02g17500 | A02 | 8720218 | G | A | splice_region_variant&intron_variant | LOW | c.2067-6G>A| |
S67 |
| 174714 | BAA02g17510 | A02 | 8720524 | G | A | upstream_gene_variant | MODIFIER | c.-1783G>A| |
S265 |
| 174715 | BAA02g17510 | A02 | 8720803 | C | T | upstream_gene_variant | MODIFIER | c.-1504C>T| |
S121 |
| 174716 | BAA02g17510 | A02 | 8722284 | C | T | upstream_gene_variant | MODIFIER | c.-23C>T| |
S139 |
| 174717 | BAA02g17510 | A02 | 8722382 | C | T | missense_variant | MODERATE | c.76C>T|p.Leu26Phe |
S44 |
| 174718 | BAA02g17510 | A02 | 8723320 | T | C | synonymous_variant | LOW | c.597T>C|p.Gly199Gly |
S20 |
| 174719 | BAA02g17500 | A02 | 8723623 | C | T | downstream_gene_variant | MODIFIER | c.*3243C>T| |
S271 |
| 174720 | BAA02g17500 | A02 | 8724033 | C | T | downstream_gene_variant | MODIFIER | c.*3653C>T| |
S272 S302 |
| 174721 | BAA02g17500 | A02 | 8724034 | C | T | downstream_gene_variant | MODIFIER | c.*3654C>T| |
S183 S198 |
| 174722 | BAA02g17500 | A02 | 8725080 | G | A | downstream_gene_variant | MODIFIER | c.*4700G>A| |
S291 |
| 174723 | BAA02g17510 | A02 | 8725406 | G | A | downstream_gene_variant | MODIFIER | c.*492G>A| |
S209 |
| 174724 | BAA02g17510 | A02 | 8725409 | G | A | downstream_gene_variant | MODIFIER | c.*495G>A| |
S229 |
| 174725 | BAA02g17510 | A02 | 8725782 | G | A | downstream_gene_variant | MODIFIER | c.*868G>A| |
S190 |