| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 197651 | BAA02g29370 | A02 | 16813936 | C | T | missense_variant | MODERATE | c.241G>A|p.Glu81Lys |
S147 S91 |
| 197652 | BAA02g29380 | A02 | 16815680 | C | T | missense_variant | MODERATE | c.2095G>A|p.Gly699Arg |
S105 S106 |
| 197653 | BAA02g29380 | A02 | 16816347 | C | T | missense_variant | MODERATE | c.1760G>A|p.Gly587Glu |
S9 |
| 197654 | BAA02g29370 | A02 | 16816614 | G | A | upstream_gene_variant | MODIFIER | c.-2258C>T| |
S153 S213 |
| 197655 | BAA02g29370 | A02 | 16816825 | C | T | upstream_gene_variant | MODIFIER | c.-2469G>A| |
S286 |
| 197656 | BAA02g29370 | A02 | 16816828 | G | A | upstream_gene_variant | MODIFIER | c.-2472C>T| |
S69 |
| 197657 | BAA02g29370 | A02 | 16816871 | C | T | upstream_gene_variant | MODIFIER | c.-2515G>A| |
S146 |
| 197658 | BAA02g29370 | A02 | 16816979 | C | T | upstream_gene_variant | MODIFIER | c.-2623G>A| |
S117 |
| 197659 | BAA02g29370 | A02 | 16817030 | G | A | upstream_gene_variant | MODIFIER | c.-2674C>T| |
S261 |
| 197660 | BAA02g29370 | A02 | 16817380 | C | T | upstream_gene_variant | MODIFIER | c.-3024G>A| |
S247 |
| 197661 | BAA02g29370 | A02 | 16817408 | C | T | upstream_gene_variant | MODIFIER | c.-3052G>A| |
S203 |
| 197662 | BAA02g29370 | A02 | 16817536 | G | A | upstream_gene_variant | MODIFIER | c.-3180C>T| |
S56 |
| 197663 | BAA02g29370 | A02 | 16818113 | C | T | upstream_gene_variant | MODIFIER | c.-3757G>A| |
S277 |
| 197664 | BAA02g29370 | A02 | 16818119 | C | T | upstream_gene_variant | MODIFIER | c.-3763G>A| |
S92 |
| 197665 | BAA02g29370 | A02 | 16818379 | G | A | upstream_gene_variant | MODIFIER | c.-4023C>T| |
S173 |
| 197666 | BAA02g29380 | A02 | 16818787 | C | T | splice_donor_variant&intron_variant | HIGH | c.1512+1G>A| |
S266 |
| 197667 | BAA02g29380 | A02 | 16818813 | G | A | missense_variant | MODERATE | c.1487C>T|p.Thr496Ile |
S207 |
| 197668 | BAA02g29380 | A02 | 16818881 | G | A | synonymous_variant | LOW | c.1419C>T|p.Asp473Asp |
S184 |
| 197669 | BAA02g29380 | A02 | 16818905 | C | T | synonymous_variant | LOW | c.1395G>A|p.Lys465Lys |
S140 |
| 197670 | BAA02g29370 | A02 | 16819026 | G | A | upstream_gene_variant | MODIFIER | c.-4670C>T| |
S251 |
| 197671 | BAA02g29380 | A02 | 16819619 | G | A | splice_region_variant&synonymous_variant | LOW | c.1152C>T|p.Leu384Leu |
S297 |
| 197672 | BAA02g29390 | A02 | 16819975 | G | A | downstream_gene_variant | MODIFIER | c.*3371C>T| |
S184 |
| 197673 | BAA02g29380 | A02 | 16820319 | G | A | missense_variant | MODERATE | c.700C>T|p.Pro234Ser |
S188 |
| 197674 | BAA02g29380 | A02 | 16820606 | G | A | missense_variant | MODERATE | c.500C>T|p.Ser167Phe |
S225 |
| 197675 | BAA02g29390 | A02 | 16820763 | C | T | downstream_gene_variant | MODIFIER | c.*2583G>A| |
S193 |