| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 184051 | BAA02g22360 | A02 | 12089968 | G | A | upstream_gene_variant | MODIFIER | c.-3075C>T| |
S272 |
| 184052 | BAA02g22360 | A02 | 12090815 | G | A | upstream_gene_variant | MODIFIER | c.-3922C>T| |
S295 |
| 184053 | BAA02g22370 | A02 | 12094584 | G | A | upstream_gene_variant | MODIFIER | c.-2761G>A| |
S47 |
| 184054 | BAA02g22370 | A02 | 12096357 | C | T | upstream_gene_variant | MODIFIER | c.-988C>T| |
S135 |
| 184055 | BAA02g22370 | A02 | 12096360 | C | T | upstream_gene_variant | MODIFIER | c.-985C>T| |
S183 S198 |
| 184056 | BAA02g22370 | A02 | 12096854 | G | A | upstream_gene_variant | MODIFIER | c.-491G>A| |
S146 |
| 184057 | BAA02g22370 | A02 | 12097439 | C | T | missense_variant | MODERATE | c.95C>T|p.Ser32Leu |
S56 |
| 184058 | BAA02g22370 | A02 | 12097711 | C | T | missense_variant | MODERATE | c.367C>T|p.Pro123Ser |
S108 |
| 184059 | BAA02g22370 | A02 | 12101184 | C | T | downstream_gene_variant | MODIFIER | c.*3204C>T| |
S49 |
| 184060 | BAA02g22370 | A02 | 12102664 | C | T | downstream_gene_variant | MODIFIER | c.*4684C>T| |
S266 |
| 184061 | BAA02g22370 | A02 | 12102931 | G | A | downstream_gene_variant | MODIFIER | c.*4951G>A| |
S297 |
| 184062 | BAA02g22370-BAA02g22380 | A02 | 12103109 | C | T | intergenic_region | MODIFIER | n.12103109C>T| |
S53 |
| 184063 | BAA02g22370-BAA02g22380 | A02 | 12103144 | C | T | intergenic_region | MODIFIER | n.12103144C>T| |
S87 |
| 184064 | BAA02g22380 | A02 | 12103615 | G | A | upstream_gene_variant | MODIFIER | c.-4794G>A| |
S45 |
| 184065 | BAA02g22380 | A02 | 12104886 | T | C | upstream_gene_variant | MODIFIER | c.-3523T>C| |
S148 S210 |
| 184066 | BAA02g22380 | A02 | 12106754 | G | A | upstream_gene_variant | MODIFIER | c.-1655G>A| |
S261 S303 |
| 184067 | BAA02g22380 | A02 | 12107534 | C | T | upstream_gene_variant | MODIFIER | c.-875C>T| |
S267 |
| 184068 | BAA02g22380 | A02 | 12108178 | G | A | upstream_gene_variant | MODIFIER | c.-231G>A| |
S288 |
| 184069 | BAA02g22380 | A02 | 12109100 | G | A | intron_variant | MODIFIER | c.80-581G>A| |
S28 |
| 184070 | BAA02g22380 | A02 | 12109187 | G | A | intron_variant | MODIFIER | c.80-494G>A| |
S59 |
| 184071 | BAA02g22380 | A02 | 12109462 | C | T | intron_variant | MODIFIER | c.80-219C>T| |
S38 |
| 184072 | BAA02g22380 | A02 | 12110623 | G | A | downstream_gene_variant | MODIFIER | c.*472G>A| |
S111 |
| 184073 | BAA02g22380 | A02 | 12112771 | G | A | downstream_gene_variant | MODIFIER | c.*2620G>A| |
S10 |
| 184074 | BAA02g22380 | A02 | 12113031 | G | A | downstream_gene_variant | MODIFIER | c.*2880G>A| |
S200 |
| 184075 | BAA02g22390 | A02 | 12114152 | C | T | upstream_gene_variant | MODIFIER | c.-4668C>T| |
S308 |