| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 56101 | BAA01g30520 | A01 | 19491392 | G | A | downstream_gene_variant | MODIFIER | c.*836G>A| |
S6 |
| 56102 | BAA01g30520 | A01 | 19491554 | G | A | downstream_gene_variant | MODIFIER | c.*998G>A| |
S172 |
| 56103 | BAA01g30520 | A01 | 19491627 | G | A | downstream_gene_variant | MODIFIER | c.*1071G>A| |
S155 S211 |
| 56104 | BAA01g30520 | A01 | 19491734 | C | T | downstream_gene_variant | MODIFIER | c.*1178C>T| |
S94 |
| 56105 | BAA01g30520 | A01 | 19492802 | C | T | downstream_gene_variant | MODIFIER | c.*2246C>T| |
S303 |
| 56106 | BAA01g30520 | A01 | 19492911 | A | G | downstream_gene_variant | MODIFIER | c.*2355A>G| |
S132 S137 S89 |
| 56107 | BAA01g30520 | A01 | 19493499 | G | A | downstream_gene_variant | MODIFIER | c.*2943G>A| |
S187 |
| 56108 | BAA01g30520 | A01 | 19493733 | G | A | downstream_gene_variant | MODIFIER | c.*3177G>A| |
S280 |
| 56109 | BAA01g30520 | A01 | 19494987 | C | A | downstream_gene_variant | MODIFIER | c.*4431C>A| |
S15 |
| 56110 | BAA01g30530 | A01 | 19495676 | G | A | downstream_gene_variant | MODIFIER | c.*1152C>T| |
S140 |
| 56111 | BAA01g30530 | A01 | 19497214 | G | A | splice_region_variant&intron_variant | LOW | c.2682+8C>T| |
S297 |
| 56112 | BAA01g30530 | A01 | 19498462 | C | T | missense_variant | MODERATE | c.1976G>A|p.Gly659Glu |
S25 S264 |
| 56113 | BAA01g30530 | A01 | 19498718 | C | T | intron_variant | MODIFIER | c.1900+16G>A| |
S249 |
| 56114 | BAA01g30530 | A01 | 19498908 | G | A | missense_variant | MODERATE | c.1726C>T|p.Arg576Trp |
S178 |
| 56115 | BAA01g30530 | A01 | 19499349 | C | T | splice_donor_variant&intron_variant | HIGH | c.1548+1G>A| |
S11 |
| 56116 | BAA01g30530 | A01 | 19499696 | G | A | intron_variant | MODIFIER | c.1317+69C>T| |
S297 |
| 56117 | BAA01g30530 | A01 | 19500423 | C | T | intron_variant | MODIFIER | c.981+48G>A| |
S171 |
| 56118 | BAA01g30530 | A01 | 19500704 | G | A | intron_variant | MODIFIER | c.861+10C>T| |
S38 |
| 56119 | BAA01g30530 | A01 | 19500819 | G | A | intron_variant | MODIFIER | c.769-13C>T| |
S202 |
| 56120 | BAA01g30530 | A01 | 19503288 | G | A | upstream_gene_variant | MODIFIER | c.-1051C>T| |
S121 |
| 56121 | BAA01g30530 | A01 | 19503681 | G | A | upstream_gene_variant | MODIFIER | c.-1444C>T| |
S121 |
| 56122 | BAA01g30530 | A01 | 19504837 | C | T | upstream_gene_variant | MODIFIER | c.-2600G>A| |
S42 |
| 56123 | BAA01g30530 | A01 | 19505043 | C | T | upstream_gene_variant | MODIFIER | c.-2806G>A| |
S17 |
| 56124 | BAA01g30530 | A01 | 19505386 | C | T | upstream_gene_variant | MODIFIER | c.-3149G>A| |
S240 |
| 56125 | BAA01g30530 | A01 | 19507039 | C | T | upstream_gene_variant | MODIFIER | c.-4802G>A| |
S67 |