| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 10551 | BAA01g08470 | A01 | 3762231 | G | A | downstream_gene_variant | MODIFIER | c.*2309G>A| |
S121 |
| 10552 | BAA01g08470 | A01 | 3762794 | G | A | downstream_gene_variant | MODIFIER | c.*2872G>A| |
S229 |
| 10553 | BAA01g08470 | A01 | 3763082 | C | T | downstream_gene_variant | MODIFIER | c.*3160C>T| |
S184 |
| 10554 | BAA01g08470 | A01 | 3763639 | G | A | downstream_gene_variant | MODIFIER | c.*3717G>A| |
S14 |
| 10555 | BAA01g08470 | A01 | 3763776 | C | T | downstream_gene_variant | MODIFIER | c.*3854C>T| |
S67 |
| 10556 | BAA01g08470 | A01 | 3764048 | G | A | downstream_gene_variant | MODIFIER | c.*4126G>A| |
S229 |
| 10557 | BAA01g08470 | A01 | 3764161 | G | A | downstream_gene_variant | MODIFIER | c.*4239G>A| |
S37 |
| 10558 | BAA01g08470 | A01 | 3764179 | C | T | downstream_gene_variant | MODIFIER | c.*4257C>T| |
S246 |
| 10559 | BAA01g08470 | A01 | 3764405 | G | A | downstream_gene_variant | MODIFIER | c.*4483G>A| |
S196 |
| 10560 | BAA01g08470-BAA01g08480 | A01 | 3765207 | C | T | intergenic_region | MODIFIER | n.3765207C>T| |
S303 |
| 10561 | BAA01g08470-BAA01g08480 | A01 | 3765322 | G | A | intergenic_region | MODIFIER | n.3765322G>A| |
S195 |
| 10562 | BAA01g08470-BAA01g08480 | A01 | 3765383 | G | A | intergenic_region | MODIFIER | n.3765383G>A| |
S57 |
| 10563 | BAA01g08480 | A01 | 3766088 | C | T | upstream_gene_variant | MODIFIER | c.-4981C>T| |
S268 |
| 10564 | BAA01g08480 | A01 | 3767440 | C | T | upstream_gene_variant | MODIFIER | c.-3629C>T| |
S112 |
| 10565 | BAA01g08480 | A01 | 3767955 | C | T | upstream_gene_variant | MODIFIER | c.-3114C>T| |
S100 |
| 10566 | BAA01g08480 | A01 | 3768350 | C | T | upstream_gene_variant | MODIFIER | c.-2719C>T| |
S134 |
| 10567 | BAA01g08480 | A01 | 3770037 | G | A | upstream_gene_variant | MODIFIER | c.-1032G>A| |
S217 S248 |
| 10568 | BAA01g08480 | A01 | 3771640 | G | A | splice_region_variant&intron_variant | LOW | c.285+5G>A| |
S190 |
| 10569 | BAA01g08480 | A01 | 3773332 | G | A | downstream_gene_variant | MODIFIER | c.*483G>A| |
S159 S243 |
| 10570 | BAA01g08500 | A01 | 3774042 | G | A | upstream_gene_variant | MODIFIER | c.-4691G>A| |
S156 |
| 10571 | BAA01g08500 | A01 | 3774852 | G | A | upstream_gene_variant | MODIFIER | c.-3881G>A| |
S208 S219 |
| 10572 | BAA01g08500 | A01 | 3776958 | C | T | upstream_gene_variant | MODIFIER | c.-1775C>T| |
S210 |
| 10573 | BAA01g08500 | A01 | 3777474 | G | A | upstream_gene_variant | MODIFIER | c.-1259G>A| |
S207 |
| 10574 | BAA01g08500 | A01 | 3778001 | C | T | upstream_gene_variant | MODIFIER | c.-732C>T| |
S16 |
| 10575 | BAA01g08500 | A01 | 3778867 | G | A | missense_variant | MODERATE | c.62G>A|p.Arg21Gln |
S287 |