| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 31351 | BAA01g21760 | A01 | 10834522 | C | T | upstream_gene_variant | MODIFIER | c.-3255G>A| |
S16 |
| 31352 | BAA01g21760 | A01 | 10834899 | G | A | upstream_gene_variant | MODIFIER | c.-3632C>T| |
S217 S248 |
| 31353 | BAA01g21760 | A01 | 10835203 | G | A | upstream_gene_variant | MODIFIER | c.-3936C>T| |
S172 S217 |
| 31354 | BAA01g21760 | A01 | 10835225 | C | T | upstream_gene_variant | MODIFIER | c.-3958G>A| |
S158 |
| 31355 | BAA01g21760 | A01 | 10835544 | C | T | upstream_gene_variant | MODIFIER | c.-4277G>A| |
S65 |
| 31356 | BAA01g21760 | A01 | 10835547 | C | T | upstream_gene_variant | MODIFIER | c.-4280G>A| |
S215 |
| 31357 | BAA01g21770 | A01 | 10836534 | C | T | upstream_gene_variant | MODIFIER | c.-4522G>A| |
S61 |
| 31358 | BAA01g21770-BAA01g21780 | A01 | 10837358 | G | A | intergenic_region | MODIFIER | n.10837358G>A| |
S263 |
| 31359 | BAA01g21780 | A01 | 10837920 | G | A | upstream_gene_variant | MODIFIER | c.-4541G>A| |
S275 |
| 31360 | BAA01g21780 | A01 | 10839220 | G | A | upstream_gene_variant | MODIFIER | c.-3241G>A| |
S244 |
| 31361 | BAA01g21780 | A01 | 10839893 | G | A | upstream_gene_variant | MODIFIER | c.-2568G>A| |
S272 S79 S91 |
| 31362 | BAA01g21780 | A01 | 10840229 | G | A | upstream_gene_variant | MODIFIER | c.-2232G>A| |
S241 |
| 31363 | BAA01g21780 | A01 | 10841040 | G | A | upstream_gene_variant | MODIFIER | c.-1421G>A| |
S217 S248 |
| 31364 | BAA01g21780 | A01 | 10841387 | C | T | upstream_gene_variant | MODIFIER | c.-1074C>T| |
S158 |
| 31365 | BAA01g21780 | A01 | 10841730 | C | T | upstream_gene_variant | MODIFIER | c.-731C>T| |
S19 |
| 31366 | BAA01g21780 | A01 | 10841823 | G | A | upstream_gene_variant | MODIFIER | c.-638G>A| |
S60 |
| 31367 | BAA01g21780 | A01 | 10842198 | C | T | upstream_gene_variant | MODIFIER | c.-263C>T| |
S259 |
| 31368 | BAA01g21780 | A01 | 10843182 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.358-1G>A| |
S144 |
| 31369 | BAA01g21780 | A01 | 10843307 | G | A | missense_variant | MODERATE | c.482G>A|p.Arg161Gln |
S192 |
| 31370 | BAA01g21790 | A01 | 10843677 | G | A | upstream_gene_variant | MODIFIER | c.-3124G>A| |
S129 |
| 31371 | BAA01g21790 | A01 | 10843778 | C | T | upstream_gene_variant | MODIFIER | c.-3023C>T| |
S87 |
| 31372 | BAA01g21790 | A01 | 10846176 | G | A | upstream_gene_variant | MODIFIER | c.-625G>A| |
S149 |
| 31373 | BAA01g21790 | A01 | 10846678 | C | T | upstream_gene_variant | MODIFIER | c.-123C>T| |
S259 |
| 31374 | BAA01g21790 | A01 | 10847865 | G | A | missense_variant | MODERATE | c.760G>A|p.Glu254Lys |
S57 |
| 31375 | BAA01g21790 | A01 | 10848023 | G | A | missense_variant | MODERATE | c.814G>A|p.Gly272Arg |
S149 |