| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 61101 | BAA01g32440 | A01 | 21377650 | C | T | upstream_gene_variant | MODIFIER | c.-3813G>A| |
S186 |
| 61102 | BAA01g32440 | A01 | 21377751 | C | T | upstream_gene_variant | MODIFIER | c.-3914G>A| |
S115 |
| 61103 | BAA01g32440 | A01 | 21378782 | G | A | upstream_gene_variant | MODIFIER | c.-4945C>T| |
S209 |
| 61104 | BAA01g32450 | A01 | 21379063 | C | T | missense_variant | MODERATE | c.1145G>A|p.Gly382Asp |
S80 |
| 61105 | BAA01g32450 | A01 | 21379165 | C | T | missense_variant | MODERATE | c.1043G>A|p.Gly348Glu |
S78 |
| 61106 | BAA01g32450 | A01 | 21379232 | C | T | missense_variant | MODERATE | c.976G>A|p.Gly326Ser |
S186 |
| 61107 | BAA01g32450 | A01 | 21379468 | C | T | missense_variant | MODERATE | c.740G>A|p.Gly247Glu |
S142 |
| 61108 | BAA01g32450 | A01 | 21379550 | C | T | missense_variant | MODERATE | c.658G>A|p.Gly220Ser |
S19 |
| 61109 | BAA01g32450 | A01 | 21381360 | C | T | upstream_gene_variant | MODIFIER | c.-1153G>A| |
S233 |
| 61110 | BAA01g32460 | A01 | 21383961 | G | A | missense_variant | MODERATE | c.122C>T|p.Ala41Val |
S223 |
| 61111 | BAA01g32460 | A01 | 21386828 | C | T | upstream_gene_variant | MODIFIER | c.-2746G>A| |
S59 |
| 61112 | BAA01g32460 | A01 | 21387910 | C | T | upstream_gene_variant | MODIFIER | c.-3828G>A| |
S273 |
| 61113 | BAA01g32460 | A01 | 21388263 | C | T | upstream_gene_variant | MODIFIER | c.-4181G>A| |
S293 |
| 61114 | BAA01g32460 | A01 | 21389017 | G | A | upstream_gene_variant | MODIFIER | c.-4935C>T| |
S117 |
| 61115 | BAA01g32470 | A01 | 21391282 | C | T | upstream_gene_variant | MODIFIER | c.-2164C>T| |
S128 |
| 61116 | BAA01g32470 | A01 | 21392994 | C | T | upstream_gene_variant | MODIFIER | c.-452C>T| |
S113 |
| 61117 | BAA01g32470 | A01 | 21393132 | C | T | upstream_gene_variant | MODIFIER | c.-314C>T| |
S88 |
| 61118 | BAA01g32470 | A01 | 21393827 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.136-1G>A| |
S169 |
| 61119 | BAA01g32470 | A01 | 21394175 | C | T | missense_variant | MODERATE | c.319C>T|p.Pro107Ser |
S125 |
| 61120 | BAA01g32470 | A01 | 21395167 | G | A | downstream_gene_variant | MODIFIER | c.*966G>A| |
S172 S217 |
| 61121 | BAA01g32470 | A01 | 21395375 | C | T | downstream_gene_variant | MODIFIER | c.*1174C>T| |
S139 |
| 61122 | BAA01g32470 | A01 | 21395736 | G | A | downstream_gene_variant | MODIFIER | c.*1535G>A| |
S4 |
| 61123 | BAA01g32470 | A01 | 21396048 | T | G | downstream_gene_variant | MODIFIER | c.*1847T>G| |
S186 |
| 61124 | BAA01g32470 | A01 | 21396049 | A | T | downstream_gene_variant | MODIFIER | c.*1848A>T| |
S186 |
| 61125 | BAA01g32470 | A01 | 21396110 | C | T | downstream_gene_variant | MODIFIER | c.*1909C>T| |
S57 |