| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 18401 | BAA01g13750 | A01 | 6535170 | G | A | upstream_gene_variant | MODIFIER | c.-2446C>T| |
S195 |
| 18402 | BAA01g13750 | A01 | 6535303 | C | T | upstream_gene_variant | MODIFIER | c.-2579G>A| |
S44 |
| 18403 | BAA01g13750 | A01 | 6535920 | C | T | upstream_gene_variant | MODIFIER | c.-3196G>A| |
S134 |
| 18404 | BAA01g13750 | A01 | 6535973 | C | T | upstream_gene_variant | MODIFIER | c.-3249G>A| |
S203 |
| 18405 | BAA01g13750 | A01 | 6536325 | C | T | upstream_gene_variant | MODIFIER | c.-3601G>A| |
S198 |
| 18406 | BAA01g13760 | A01 | 6537927 | C | T | downstream_gene_variant | MODIFIER | c.*2831C>T| |
S182 |
| 18407 | BAA01g13770 | A01 | 6540273 | G | A | intron_variant | MODIFIER | c.312+638C>T| |
S159 S243 |
| 18408 | BAA01g13770 | A01 | 6540445 | C | T | intron_variant | MODIFIER | c.312+466G>A| |
S135 |
| 18409 | BAA01g13770 | A01 | 6540628 | G | A | intron_variant | MODIFIER | c.312+283C>T| |
S161 |
| 18410 | BAA01g13770 | A01 | 6540763 | C | T | intron_variant | MODIFIER | c.312+148G>A| |
S153 |
| 18411 | BAA01g13770 | A01 | 6543917 | G | A | upstream_gene_variant | MODIFIER | c.-2695C>T| |
S193 |
| 18412 | BAA01g13770 | A01 | 6546183 | C | T | upstream_gene_variant | MODIFIER | c.-4961G>A| |
S192 |
| 18413 | BAA01g13780 | A01 | 6546815 | C | T | upstream_gene_variant | MODIFIER | c.-3741C>T| |
S38 |
| 18414 | BAA01g13780 | A01 | 6547494 | C | T | upstream_gene_variant | MODIFIER | c.-3062C>T| |
S291 |
| 18415 | BAA01g13780 | A01 | 6547981 | G | A | upstream_gene_variant | MODIFIER | c.-2575G>A| |
S37 |
| 18416 | BAA01g13780 | A01 | 6550779 | G | A | missense_variant | MODERATE | c.224G>A|p.Gly75Asp |
S165 |
| 18417 | BAA01g13780 | A01 | 6550997 | G | A | missense_variant | MODERATE | c.442G>A|p.Gly148Ser |
S178 |
| 18418 | BAA01g13790 | A01 | 6551980 | G | A | synonymous_variant | LOW | c.66G>A|p.Arg22Arg |
S236 |
| 18419 | BAA01g13790 | A01 | 6552044 | C | T | missense_variant | MODERATE | c.130C>T|p.Pro44Ser |
S303 |
| 18420 | BAA01g13790 | A01 | 6552523 | G | A | synonymous_variant | LOW | c.609G>A|p.Glu203Glu |
S186 |
| 18421 | BAA01g13790 | A01 | 6553711 | C | T | synonymous_variant | LOW | c.1182C>T|p.Leu394Leu |
S132 S137 S89 |
| 18422 | BAA01g13780 | A01 | 6554776 | C | T | downstream_gene_variant | MODIFIER | c.*3699C>T| |
S143 |
| 18423 | BAA01g13780 | A01 | 6555533 | G | A | downstream_gene_variant | MODIFIER | c.*4456G>A| |
S183 |
| 18424 | BAA01g13790 | A01 | 6556555 | G | A | downstream_gene_variant | MODIFIER | c.*2246G>A| |
S74 |
| 18425 | BAA01g13790 | A01 | 6556918 | G | A | downstream_gene_variant | MODIFIER | c.*2609G>A| |
S257 |