| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 162651 | BAA02g09520 | A02 | 4204835 | G | A | upstream_gene_variant | MODIFIER | c.-4369C>T| |
S45 |
| 162652 | BAA02g09520 | A02 | 4205320 | T | A | upstream_gene_variant | MODIFIER | c.-4854A>T| |
S266 |
| 162653 | BAA02g09520 | A02 | 4205428 | C | T | upstream_gene_variant | MODIFIER | c.-4962G>A| |
S178 |
| 162654 | BAA02g09540 | A02 | 4205633 | C | T | upstream_gene_variant | MODIFIER | c.-1488G>A| |
S203 |
| 162655 | BAA02g09540 | A02 | 4206847 | G | A | upstream_gene_variant | MODIFIER | c.-2702C>T| |
S13 S164 |
| 162656 | BAA02g09540 | A02 | 4207177 | G | T | upstream_gene_variant | MODIFIER | c.-3032C>A| |
S107 S131 S255 S53 |
| 162657 | BAA02g09540 | A02 | 4207936 | C | T | upstream_gene_variant | MODIFIER | c.-3791G>A| |
S262 |
| 162658 | BAA02g09540 | A02 | 4208260 | G | A | upstream_gene_variant | MODIFIER | c.-4115C>T| |
S67 |
| 162659 | BAA02g09540 | A02 | 4209025 | C | T | upstream_gene_variant | MODIFIER | c.-4880G>A| |
S28 |
| 162660 | BAA02g09550 | A02 | 4209738 | G | A | missense_variant | MODERATE | c.50C>T|p.Ala17Val |
S237 |
| 162661 | BAA02g09560 | A02 | 4211367 | C | T | synonymous_variant | LOW | c.72C>T|p.Ser24Ser |
S306 S308 |
| 162662 | BAA02g09560 | A02 | 4211633 | C | T | synonymous_variant | LOW | c.243C>T|p.Tyr81Tyr |
S209 |
| 162663 | BAA02g09560 | A02 | 4211668 | C | T | missense_variant | MODERATE | c.278C>T|p.Ala93Val |
S251 |
| 162664 | BAA02g09550 | A02 | 4212801 | G | A | upstream_gene_variant | MODIFIER | c.-3014C>T| |
S105 S106 S6 |
| 162665 | BAA02g09550 | A02 | 4213712 | G | A | upstream_gene_variant | MODIFIER | c.-3925C>T| |
S197 |
| 162666 | BAA02g09560 | A02 | 4214697 | G | A | missense_variant | MODERATE | c.554G>A|p.Arg185Lys |
S236 |
| 162667 | BAA02g09560 | A02 | 4214913 | C | T | missense_variant | MODERATE | c.695C>T|p.Pro232Leu |
S128 |
| 162668 | BAA02g09590 | A02 | 4218504 | C | T | upstream_gene_variant | MODIFIER | c.-2869C>T| |
S286 |
| 162669 | BAA02g09580 | A02 | 4218724 | G | A | stop_gained | HIGH | c.307C>T|p.Gln103* |
S264 |
| 162670 | BAA02g09590 | A02 | 4218793 | G | A | upstream_gene_variant | MODIFIER | c.-2580G>A| |
S12 |
| 162671 | BAA02g09590 | A02 | 4218805 | C | T | upstream_gene_variant | MODIFIER | c.-2568C>T| |
S120 |
| 162672 | BAA02g09580 | A02 | 4219514 | C | T | upstream_gene_variant | MODIFIER | c.-14G>A| |
S103 |
| 162673 | BAA02g09580 | A02 | 4220020 | C | T | upstream_gene_variant | MODIFIER | c.-520G>A| |
S266 |
| 162674 | BAA02g09580 | A02 | 4220071 | C | T | upstream_gene_variant | MODIFIER | c.-571G>A| |
S262 |
| 162675 | BAA02g09580 | A02 | 4220331 | C | T | upstream_gene_variant | MODIFIER | c.-831G>A| |
S224 |