| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 31301 | BAA01g21740 | A01 | 10822158 | C | T | upstream_gene_variant | MODIFIER | c.-1859G>A| |
S148 S30 S31 |
| 31302 | BAA01g21740 | A01 | 10822228 | C | T | upstream_gene_variant | MODIFIER | c.-1929G>A| |
S134 |
| 31303 | BAA01g21750 | A01 | 10822698 | G | A | synonymous_variant | LOW | c.405G>A|p.Pro135Pro |
S296 |
| 31304 | BAA01g21740 | A01 | 10822981 | C | T | upstream_gene_variant | MODIFIER | c.-2682G>A| |
S287 |
| 31305 | BAA01g21740 | A01 | 10824835 | C | T | upstream_gene_variant | MODIFIER | c.-4536G>A| |
S282 |
| 31306 | BAA01g21740 | A01 | 10824882 | G | A | upstream_gene_variant | MODIFIER | c.-4583C>T| |
S298 |
| 31307 | BAA01g21750 | A01 | 10826174 | C | T | downstream_gene_variant | MODIFIER | c.*3296C>T| |
S267 |
| 31308 | BAA01g21750 | A01 | 10826211 | G | A | downstream_gene_variant | MODIFIER | c.*3333G>A| |
S49 |
| 31309 | BAA01g21750 | A01 | 10826441 | C | T | downstream_gene_variant | MODIFIER | c.*3563C>T| |
S135 |
| 31310 | BAA01g21750 | A01 | 10826801 | C | T | downstream_gene_variant | MODIFIER | c.*3923C>T| |
S266 |
| 31311 | BAA01g21760 | A01 | 10828393 | G | A | downstream_gene_variant | MODIFIER | c.*2101C>T| |
S188 |
| 31312 | BAA01g21760 | A01 | 10829370 | G | A | downstream_gene_variant | MODIFIER | c.*1124C>T| |
S5 |
| 31313 | BAA01g21760 | A01 | 10829680 | G | A | downstream_gene_variant | MODIFIER | c.*814C>T| |
S259 |
| 31314 | BAA01g21760 | A01 | 10830032 | C | T | downstream_gene_variant | MODIFIER | c.*462G>A| |
S99 |
| 31315 | BAA01g21760 | A01 | 10830823 | C | T | missense_variant | MODERATE | c.175G>A|p.Val59Met |
S179 |
| 31316 | BAA01g21760 | A01 | 10830971 | G | A | synonymous_variant | LOW | c.27C>T|p.Pro9Pro |
S15 S3 |
| 31317 | BAA01g21770 | A01 | 10831055 | G | A | downstream_gene_variant | MODIFIER | c.*260C>T| |
S84 S93 |
| 31318 | BAA01g21770 | A01 | 10831596 | C | A | missense_variant | MODERATE | c.151G>T|p.Asp51Tyr |
S130 |
| 31319 | BAA01g21770 | A01 | 10831598 | C | G | missense_variant | MODERATE | c.149G>C|p.Arg50Thr |
S130 |
| 31320 | BAA01g21770 | A01 | 10831996 | G | A | missense_variant | MODERATE | c.17C>T|p.Ser6Phe |
S9 |
| 31321 | BAA01g21760 | A01 | 10832432 | C | T | upstream_gene_variant | MODIFIER | c.-1165G>A| |
S270 |
| 31322 | BAA01g21760 | A01 | 10833879 | C | T | upstream_gene_variant | MODIFIER | c.-2612G>A| |
S87 |
| 31323 | BAA01g21760 | A01 | 10834000 | C | T | upstream_gene_variant | MODIFIER | c.-2733G>A| |
S108 |
| 31324 | BAA01g21760 | A01 | 10834084 | G | A | upstream_gene_variant | MODIFIER | c.-2817C>T| |
S274 |
| 31325 | BAA01g21760 | A01 | 10834340 | C | T | upstream_gene_variant | MODIFIER | c.-3073G>A| |
S179 |