| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 183601 | BAA02g22120 | A02 | 11923293 | G | A | upstream_gene_variant | MODIFIER | c.-3931C>T| |
S279 |
| 183602 | BAA02g22120 | A02 | 11923744 | A | T | upstream_gene_variant | MODIFIER | c.-4382T>A| |
S149 |
| 183603 | BAA02g22130 | A02 | 11925183 | C | T | missense_variant | MODERATE | c.377C>T|p.Ala126Val |
S289 S290 |
| 183604 | BAA02g22130 | A02 | 11925898 | C | T | intron_variant | MODIFIER | c.853-50C>T| |
S212 |
| 183605 | BAA02g22130 | A02 | 11926309 | C | T | missense_variant | MODERATE | c.1138C>T|p.Leu380Phe |
S267 |
| 183606 | BAA02g22130 | A02 | 11926588 | G | A | missense_variant | MODERATE | c.1417G>A|p.Gly473Arg |
S177 |
| 183607 | BAA02g22140 | A02 | 11926993 | G | A | upstream_gene_variant | MODIFIER | c.-4812G>A| |
S33 |
| 183608 | BAA02g22140 | A02 | 11927058 | G | A | upstream_gene_variant | MODIFIER | c.-4747G>A| |
S12 |
| 183609 | BAA02g22140 | A02 | 11927375 | G | A | upstream_gene_variant | MODIFIER | c.-4430G>A| |
S7 |
| 183610 | BAA02g22140 | A02 | 11927963 | G | A | upstream_gene_variant | MODIFIER | c.-3842G>A| |
S184 |
| 183611 | BAA02g22140 | A02 | 11928719 | G | A | upstream_gene_variant | MODIFIER | c.-3086G>A| |
S43 |
| 183612 | BAA02g22140 | A02 | 11929158 | C | T | upstream_gene_variant | MODIFIER | c.-2647C>T| |
S82 S92 |
| 183613 | BAA02g22140 | A02 | 11929460 | C | T | upstream_gene_variant | MODIFIER | c.-2345C>T| |
S81 |
| 183614 | BAA02g22140 | A02 | 11929707 | C | T | upstream_gene_variant | MODIFIER | c.-2098C>T| |
S185 |
| 183615 | BAA02g22140 | A02 | 11930766 | G | A | upstream_gene_variant | MODIFIER | c.-1039G>A| |
S297 |
| 183616 | BAA02g22140 | A02 | 11930880 | C | T | upstream_gene_variant | MODIFIER | c.-925C>T| |
S250 |
| 183617 | BAA02g22140 | A02 | 11931324 | C | T | upstream_gene_variant | MODIFIER | c.-481C>T| |
S84 S93 |
| 183618 | BAA02g22140 | A02 | 11931790 | G | A | upstream_gene_variant | MODIFIER | c.-15G>A| |
S237 |
| 183619 | BAA02g22140 | A02 | 11931982 | G | A | missense_variant | MODERATE | c.178G>A|p.Asp60Asn |
S132 S215 |
| 183620 | BAA02g22140 | A02 | 11932515 | G | A | missense_variant | MODERATE | c.632G>A|p.Arg211Lys |
S281 |
| 183621 | BAA02g22140 | A02 | 11932679 | C | T | splice_region_variant&intron_variant | LOW | c.700-3C>T| |
S1 S90 |
| 183622 | BAA02g22150 | A02 | 11933164 | C | T | downstream_gene_variant | MODIFIER | c.*1856G>A| |
S99 |
| 183623 | BAA02g22140 | A02 | 11933439 | G | A | missense_variant | MODERATE | c.1206G>A|p.Met402Ile |
S202 |
| 183624 | BAA02g22160 | A02 | 11934979 | C | T | upstream_gene_variant | MODIFIER | c.-4423C>T| |
S51 |
| 183625 | BAA02g22150 | A02 | 11936927 | C | T | missense_variant | MODERATE | c.493G>A|p.Glu165Lys |
S193 |