| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 16701 | BAA01g12650 | A01 | 5972277 | C | T | synonymous_variant | LOW | c.792G>A|p.Glu264Glu |
S184 |
| 16702 | BAA01g12650 | A01 | 5974696 | C | T | upstream_gene_variant | MODIFIER | c.-1628G>A| |
S54 |
| 16703 | BAA01g12660 | A01 | 5976152 | C | T | synonymous_variant | LOW | c.414C>T|p.Ser138Ser |
S252 |
| 16704 | BAA01g12660 | A01 | 5976187 | G | A | missense_variant | MODERATE | c.449G>A|p.Gly150Glu |
S274 |
| 16705 | BAA01g12660 | A01 | 5976285 | G | A | missense_variant | MODERATE | c.547G>A|p.Gly183Arg |
S276 |
| 16706 | BAA01g12660 | A01 | 5976845 | G | A | synonymous_variant | LOW | c.1107G>A|p.Lys369Lys |
S218 |
| 16707 | BAA01g12650 | A01 | 5977792 | C | T | upstream_gene_variant | MODIFIER | c.-4724G>A| |
S48 |
| 16708 | BAA01g12680 | A01 | 5981363 | G | A | upstream_gene_variant | MODIFIER | c.-4230G>A| |
S280 |
| 16709 | BAA01g12680 | A01 | 5981588 | C | T | upstream_gene_variant | MODIFIER | c.-4005C>T| |
S264 |
| 16710 | BAA01g12680 | A01 | 5982107 | G | A | upstream_gene_variant | MODIFIER | c.-3486G>A| |
S183 S198 |
| 16711 | BAA01g12680 | A01 | 5982852 | G | A | upstream_gene_variant | MODIFIER | c.-2741G>A| |
S251 |
| 16712 | BAA01g12680 | A01 | 5983177 | G | A | upstream_gene_variant | MODIFIER | c.-2416G>A| |
S238 |
| 16713 | BAA01g12680 | A01 | 5984452 | C | T | upstream_gene_variant | MODIFIER | c.-1141C>T| |
S146 |
| 16714 | BAA01g12680 | A01 | 5985827 | C | T | missense_variant | MODERATE | c.235C>T|p.Pro79Ser |
S25 |
| 16715 | BAA01g12680 | A01 | 5986664 | C | T | missense_variant | MODERATE | c.1072C>T|p.Leu358Phe |
S208 S93 |
| 16716 | BAA01g12680 | A01 | 5986805 | C | T | missense_variant | MODERATE | c.1213C>T|p.Pro405Ser |
S242 |
| 16717 | BAA01g12690 | A01 | 5987272 | G | A | upstream_gene_variant | MODIFIER | c.-4264G>A| |
S138 |
| 16718 | BAA01g12690 | A01 | 5987387 | G | A | upstream_gene_variant | MODIFIER | c.-4149G>A| |
S293 |
| 16719 | BAA01g12690 | A01 | 5987634 | G | A | upstream_gene_variant | MODIFIER | c.-3902G>A| |
S181 |
| 16720 | BAA01g12690 | A01 | 5989010 | G | A | upstream_gene_variant | MODIFIER | c.-2526G>A| |
S280 |
| 16721 | BAA01g12690 | A01 | 5989084 | G | A | upstream_gene_variant | MODIFIER | c.-2452G>A| |
S245 |
| 16722 | BAA01g12690 | A01 | 5989722 | C | T | upstream_gene_variant | MODIFIER | c.-1814C>T| |
S35 |
| 16723 | BAA01g12690 | A01 | 5990128 | G | A | upstream_gene_variant | MODIFIER | c.-1408G>A| |
S236 |
| 16724 | BAA01g12690 | A01 | 5991523 | C | T | upstream_gene_variant | MODIFIER | c.-13C>T| |
S78 |
| 16725 | BAA01g12690 | A01 | 5991741 | G | A | missense_variant | MODERATE | c.206G>A|p.Arg69His |
S133 |