| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 176601 | BAA02g18430 | A02 | 9411789 | G | A | upstream_gene_variant | MODIFIER | c.-4124C>T| |
S296 |
| 176602 | BAA02g18430 | A02 | 9412521 | G | A | upstream_gene_variant | MODIFIER | c.-4856C>T| |
S187 |
| 176603 | BAA02g18460 | A02 | 9413104 | C | T | splice_region_variant&stop_retained_variant | LOW | c.1172G>A|p.Ter391Ter |
S305 |
| 176604 | BAA02g18460 | A02 | 9413410 | G | A | missense_variant | MODERATE | c.866C>T|p.Pro289Leu |
S143 |
| 176605 | BAA02g18460 | A02 | 9413696 | C | T | missense_variant | MODERATE | c.580G>A|p.Asp194Asn |
S206 |
| 176606 | BAA02g18460 | A02 | 9413926 | C | T | missense_variant | MODERATE | c.350G>A|p.Ser117Asn |
S179 |
| 176607 | BAA02g18450 | A02 | 9414316 | G | A | upstream_gene_variant | MODIFIER | c.-2538C>T| |
S111 |
| 176608 | BAA02g18470 | A02 | 9415031 | C | T | synonymous_variant | LOW | c.453G>A|p.Gly151Gly |
S128 |
| 176609 | BAA02g18450 | A02 | 9415750 | G | A | upstream_gene_variant | MODIFIER | c.-3972C>T| |
S294 |
| 176610 | BAA02g18450 | A02 | 9416096 | G | A | upstream_gene_variant | MODIFIER | c.-4318C>T| |
S168 |
| 176611 | BAA02g18450 | A02 | 9416122 | G | A | upstream_gene_variant | MODIFIER | c.-4344C>T| |
S203 |
| 176612 | BAA02g18480 | A02 | 9419117 | C | T | missense_variant | MODERATE | c.1580G>A|p.Gly527Glu |
S249 |
| 176613 | BAA02g18470 | A02 | 9419565 | G | A | upstream_gene_variant | MODIFIER | c.-3901C>T| |
S298 |
| 176614 | BAA02g18470 | A02 | 9419796 | T | C | upstream_gene_variant | MODIFIER | c.-4132A>G| |
S263 |
| 176615 | BAA02g18470 | A02 | 9420610 | G | A | upstream_gene_variant | MODIFIER | c.-4946C>T| |
S216 |
| 176616 | BAA02g18480 | A02 | 9420697 | C | T | intron_variant | MODIFIER | c.1281+867G>A| |
S108 |
| 176617 | BAA02g18480 | A02 | 9421157 | C | T | intron_variant | MODIFIER | c.1281+407G>A| |
S180 |
| 176618 | BAA02g18480 | A02 | 9421264 | G | A | intron_variant | MODIFIER | c.1281+300C>T| |
S293 |
| 176619 | BAA02g18480 | A02 | 9421465 | G | A | intron_variant | MODIFIER | c.1281+99C>T| |
S236 |
| 176620 | BAA02g18480 | A02 | 9421559 | C | T | splice_region_variant&intron_variant | LOW | c.1281+5G>A| |
S100 |
| 176621 | BAA02g18480 | A02 | 9423637 | G | A | upstream_gene_variant | MODIFIER | c.-374C>T| |
S61 |
| 176622 | BAA02g18480 | A02 | 9423769 | C | T | upstream_gene_variant | MODIFIER | c.-506G>A| |
S207 |
| 176623 | BAA02g18480 | A02 | 9423771 | G | A | upstream_gene_variant | MODIFIER | c.-508C>T| |
S56 |
| 176624 | BAA02g18480 | A02 | 9425064 | G | A | upstream_gene_variant | MODIFIER | c.-1801C>T| |
S11 |
| 176625 | BAA02g18480 | A02 | 9426168 | C | T | upstream_gene_variant | MODIFIER | c.-2905G>A| |
S181 |