| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 182201 | BAA02g21270 | A02 | 11410628 | C | T | upstream_gene_variant | MODIFIER | c.-4836G>A| |
S18 |
| 182202 | BAA02g21280 | A02 | 11411100 | C | T | upstream_gene_variant | MODIFIER | c.-2797C>T| |
S181 |
| 182203 | BAA02g21280 | A02 | 11411125 | C | T | upstream_gene_variant | MODIFIER | c.-2772C>T| |
S53 |
| 182204 | BAA02g21280 | A02 | 11414405 | C | T | missense_variant | MODERATE | c.509C>T|p.Thr170Met |
S6 |
| 182205 | BAA02g21280 | A02 | 11415004 | G | A | synonymous_variant | LOW | c.639G>A|p.Gly213Gly |
S272 |
| 182206 | BAA02g21280 | A02 | 11415129 | G | A | missense_variant | MODERATE | c.764G>A|p.Gly255Glu |
S111 |
| 182207 | BAA02g21280 | A02 | 11415267 | G | A | missense_variant | MODERATE | c.902G>A|p.Gly301Glu |
S5 |
| 182208 | BAA02g21280 | A02 | 11416033 | C | T | downstream_gene_variant | MODIFIER | c.*399C>T| |
S218 |
| 182209 | BAA02g21280 | A02 | 11416237 | C | T | downstream_gene_variant | MODIFIER | c.*603C>T| |
S80 |
| 182210 | BAA02g21280 | A02 | 11416395 | C | T | downstream_gene_variant | MODIFIER | c.*761C>T| |
S178 |
| 182211 | BAA02g21280 | A02 | 11416474 | G | A | downstream_gene_variant | MODIFIER | c.*840G>A| |
S59 |
| 182212 | BAA02g21290 | A02 | 11418283 | G | A | upstream_gene_variant | MODIFIER | c.-354C>T| |
S295 |
| 182213 | BAA02g21300 | A02 | 11418785 | G | A | missense_variant | MODERATE | c.715C>T|p.Pro239Ser |
S238 |
| 182214 | BAA02g21300 | A02 | 11418828 | C | T | splice_region_variant&intron_variant | LOW | c.676-4G>A| |
S25 |
| 182215 | BAA02g21300 | A02 | 11419816 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.310-1G>A| |
S25 |
| 182216 | BAA02g21290 | A02 | 11422794 | G | A | upstream_gene_variant | MODIFIER | c.-4865C>T| |
S278 |
| 182217 | BAA02g21300 | A02 | 11424820 | G | A | upstream_gene_variant | MODIFIER | c.-2280C>T| |
S279 |
| 182218 | BAA02g21310 | A02 | 11425686 | G | A | missense_variant | MODERATE | c.20C>T|p.Ser7Leu |
S236 |
| 182219 | BAA02g21300 | A02 | 11426250 | G | A | upstream_gene_variant | MODIFIER | c.-3710C>T| |
S293 |
| 182220 | BAA02g21300 | A02 | 11426570 | G | A | upstream_gene_variant | MODIFIER | c.-4030C>T| |
S239 |
| 182221 | BAA02g21300 | A02 | 11426718 | G | A | upstream_gene_variant | MODIFIER | c.-4178C>T| |
S281 |
| 182222 | BAA02g21310 | A02 | 11428020 | G | A | upstream_gene_variant | MODIFIER | c.-2315C>T| |
S190 |
| 182223 | BAA02g21310 | A02 | 11428128 | C | T | upstream_gene_variant | MODIFIER | c.-2423G>A| |
S206 S9 |
| 182224 | BAA02g21310 | A02 | 11430352 | G | A | upstream_gene_variant | MODIFIER | c.-4647C>T| |
S159 S243 |
| 182225 | BAA02g21320 | A02 | 11432436 | C | T | upstream_gene_variant | MODIFIER | c.-441C>T| |
S107 |