| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 171001 | BAA02g15410 | A02 | 7411509 | C | T | downstream_gene_variant | MODIFIER | c.*1519C>T| |
S121 |
| 171002 | BAA02g15410 | A02 | 7411963 | G | A | downstream_gene_variant | MODIFIER | c.*1973G>A| |
S193 |
| 171003 | BAA02g15410 | A02 | 7411965 | G | A | downstream_gene_variant | MODIFIER | c.*1975G>A| |
S134 |
| 171004 | BAA02g15410 | A02 | 7412999 | C | T | downstream_gene_variant | MODIFIER | c.*3009C>T| |
S28 |
| 171005 | BAA02g15410 | A02 | 7413297 | G | A | downstream_gene_variant | MODIFIER | c.*3307G>A| |
S43 |
| 171006 | BAA02g15410 | A02 | 7414000 | C | T | downstream_gene_variant | MODIFIER | c.*4010C>T| |
S212 |
| 171007 | BAA02g15420 | A02 | 7415577 | C | T | downstream_gene_variant | MODIFIER | c.*807G>A| |
S195 |
| 171008 | BAA02g15420 | A02 | 7415674 | G | A | downstream_gene_variant | MODIFIER | c.*710C>T| |
S132 S137 S215 |
| 171009 | BAA02g15420 | A02 | 7416478 | C | T | missense_variant | MODERATE | c.632G>A|p.Gly211Glu |
S218 |
| 171010 | BAA02g15420 | A02 | 7419083 | G | A | upstream_gene_variant | MODIFIER | c.-1974C>T| |
S67 |
| 171011 | BAA02g15420 | A02 | 7420506 | C | T | upstream_gene_variant | MODIFIER | c.-3397G>A| |
S174 S27 |
| 171012 | BAA02g15420 | A02 | 7421445 | G | A | upstream_gene_variant | MODIFIER | c.-4336C>T| |
S124 |
| 171013 | BAA02g15420 | A02 | 7421683 | C | T | upstream_gene_variant | MODIFIER | c.-4574G>A| |
S138 |
| 171014 | BAA02g15420 | A02 | 7422023 | G | A | upstream_gene_variant | MODIFIER | c.-4914C>T| |
S177 |
| 171015 | BAA02g15430 | A02 | 7422350 | G | A | upstream_gene_variant | MODIFIER | c.-2324C>T| |
S45 |
| 171016 | BAA02g15430 | A02 | 7423718 | C | T | upstream_gene_variant | MODIFIER | c.-3692G>A| |
S212 |
| 171017 | BAA02g15430-BAA02g15440 | A02 | 7425185 | C | T | intergenic_region | MODIFIER | n.7425185C>T| |
S62 |
| 171018 | BAA02g15430-BAA02g15440 | A02 | 7427532 | G | A | intergenic_region | MODIFIER | n.7427532G>A| |
S37 |
| 171019 | BAA02g15430-BAA02g15440 | A02 | 7432441 | G | A | intergenic_region | MODIFIER | n.7432441G>A| |
S172 S217 |
| 171020 | BAA02g15430-BAA02g15440 | A02 | 7434096 | C | T | intergenic_region | MODIFIER | n.7434096C>T| |
S40 S49 |
| 171021 | BAA02g15430-BAA02g15440 | A02 | 7434211 | C | T | intergenic_region | MODIFIER | n.7434211C>T| |
S198 |
| 171022 | BAA02g15440 | A02 | 7435130 | G | A | downstream_gene_variant | MODIFIER | c.*4742C>T| |
S129 |
| 171023 | BAA02g15440 | A02 | 7439608 | C | T | downstream_gene_variant | MODIFIER | c.*264G>A| |
S174 S27 |
| 171024 | BAA02g15440 | A02 | 7439916 | C | T | missense_variant | MODERATE | c.1663G>A|p.Glu555Lys |
S152 |
| 171025 | BAA02g15440 | A02 | 7440344 | A | G | intron_variant | MODIFIER | c.1302+19T>C| |
S62 |