| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 77151 | BAA01g40740 | A01 | 27003675 | G | A | synonymous_variant | LOW | c.3240G>A|p.Arg1080Arg |
S173 |
| 77152 | BAA01g40730 | A01 | 27004290 | A | C | downstream_gene_variant | MODIFIER | c.*4325A>C| |
S23 |
| 77153 | BAA01g40730 | A01 | 27004503 | G | A | downstream_gene_variant | MODIFIER | c.*4538G>A| |
S39 |
| 77154 | BAA01g40730 | A01 | 27004515 | C | T | downstream_gene_variant | MODIFIER | c.*4550C>T| |
S39 |
| 77155 | BAA01g40730 | A01 | 27004531 | T | A | downstream_gene_variant | MODIFIER | c.*4566T>A| |
S39 |
| 77156 | BAA01g40750 | A01 | 27005933 | C | T | synonymous_variant | LOW | c.1047G>A|p.Lys349Lys |
S16 |
| 77157 | BAA01g40750 | A01 | 27006012 | C | T | missense_variant | MODERATE | c.968G>A|p.Gly323Glu |
S275 |
| 77158 | BAA01g40750 | A01 | 27006430 | C | T | missense_variant | MODERATE | c.550G>A|p.Glu184Lys |
S42 |
| 77159 | BAA01g40750 | A01 | 27007465 | C | T | synonymous_variant | LOW | c.303G>A|p.Val101Val |
S288 |
| 77160 | BAA01g40750 | A01 | 27007558 | C | T | synonymous_variant | LOW | c.210G>A|p.Ala70Ala |
S28 |
| 77161 | BAA01g40750 | A01 | 27007700 | G | A | missense_variant | MODERATE | c.68C>T|p.Ser23Phe |
S95 |
| 77162 | BAA01g40750 | A01 | 27009570 | G | A | upstream_gene_variant | MODIFIER | c.-1803C>T| |
S189 |
| 77163 | BAA01g40750 | A01 | 27009648 | C | T | upstream_gene_variant | MODIFIER | c.-1881G>A| |
S198 |
| 77164 | BAA01g40750 | A01 | 27010157 | C | T | upstream_gene_variant | MODIFIER | c.-2390G>A| |
S171 |
| 77165 | BAA01g40760 | A01 | 27013445 | C | T | upstream_gene_variant | MODIFIER | c.-820C>T| |
S264 |
| 77166 | BAA01g40770 | A01 | 27015224 | C | A | upstream_gene_variant | MODIFIER | c.-3749C>A| |
S51 |
| 77167 | BAA01g40760 | A01 | 27015764 | G | A | missense_variant | MODERATE | c.955G>A|p.Asp319Asn |
S124 |
| 77168 | BAA01g40760 | A01 | 27015798 | C | T | missense_variant | MODERATE | c.989C>T|p.Pro330Leu |
S231 |
| 77169 | BAA01g40760 | A01 | 27016067 | G | A | missense_variant | MODERATE | c.1258G>A|p.Ala420Thr |
S172 S217 |
| 77170 | BAA01g40770 | A01 | 27018144 | C | T | upstream_gene_variant | MODIFIER | c.-829C>T| |
S28 |
| 77171 | BAA01g40770 | A01 | 27018807 | C | T | upstream_gene_variant | MODIFIER | c.-166C>T| |
S132 S215 |
| 77172 | BAA01g40770 | A01 | 27019045 | C | T | missense_variant | MODERATE | c.73C>T|p.Pro25Ser |
S282 |
| 77173 | BAA01g40770 | A01 | 27019320 | C | T | missense_variant | MODERATE | c.260C>T|p.Ala87Val |
S82 S92 |
| 77174 | BAA01g40780 | A01 | 27020408 | G | A | upstream_gene_variant | MODIFIER | c.-1603G>A| |
S298 |
| 77175 | BAA01g40780 | A01 | 27020494 | C | T | upstream_gene_variant | MODIFIER | c.-1517C>T| |
S251 |