| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 27151 | BAA01g19250 | A01 | 9470595 | C | T | upstream_gene_variant | MODIFIER | c.-1160G>A| |
S128 |
| 27152 | BAA01g19250 | A01 | 9471072 | G | A | upstream_gene_variant | MODIFIER | c.-1637C>T| |
S257 |
| 27153 | BAA01g19250 | A01 | 9471210 | G | A | upstream_gene_variant | MODIFIER | c.-1775C>T| |
S240 |
| 27154 | BAA01g19250 | A01 | 9472052 | C | T | upstream_gene_variant | MODIFIER | c.-2617G>A| |
S264 |
| 27155 | BAA01g19250 | A01 | 9473163 | C | T | upstream_gene_variant | MODIFIER | c.-3728G>A| |
S256 |
| 27156 | BAA01g19250 | A01 | 9474265 | G | A | upstream_gene_variant | MODIFIER | c.-4830C>T| |
S72 S78 |
| 27157 | BAA01g19250 | A01 | 9474361 | G | A | upstream_gene_variant | MODIFIER | c.-4926C>T| |
S257 |
| 27158 | BAA01g19260 | A01 | 9474970 | G | A | downstream_gene_variant | MODIFIER | c.*1706C>T| |
S142 |
| 27159 | BAA01g19260 | A01 | 9474985 | G | A | downstream_gene_variant | MODIFIER | c.*1691C>T| |
S12 |
| 27160 | BAA01g19260 | A01 | 9475040 | C | T | downstream_gene_variant | MODIFIER | c.*1636G>A| |
S130 |
| 27161 | BAA01g19260 | A01 | 9475046 | C | T | downstream_gene_variant | MODIFIER | c.*1630G>A| |
S134 |
| 27162 | BAA01g19270 | A01 | 9476513 | C | T | upstream_gene_variant | MODIFIER | c.-3870C>T| |
S82 S92 |
| 27163 | BAA01g19260 | A01 | 9476723 | G | A | splice_region_variant&intron_variant | LOW | c.2794-6C>T| |
S109 |
| 27164 | BAA01g19260 | A01 | 9476851 | C | T | missense_variant | MODERATE | c.2746G>A|p.Val916Ile |
S118 |
| 27165 | BAA01g19260 | A01 | 9476874 | G | A | missense_variant | MODERATE | c.2723C>T|p.Ser908Phe |
S195 |
| 27166 | BAA01g19260 | A01 | 9478006 | G | A | synonymous_variant | LOW | c.1854C>T|p.Leu618Leu |
S280 |
| 27167 | BAA01g19260 | A01 | 9478037 | G | A | missense_variant | MODERATE | c.1823C>T|p.Ser608Phe |
S245 |
| 27168 | BAA01g19260 | A01 | 9478687 | G | A | synonymous_variant | LOW | c.1173C>T|p.Leu391Leu |
S165 |
| 27169 | BAA01g19260 | A01 | 9478835 | C | T | missense_variant | MODERATE | c.1025G>A|p.Gly342Glu |
S146 |
| 27170 | BAA01g19260 | A01 | 9479442 | C | A | stop_gained | HIGH | c.418G>T|p.Glu140* |
S64 |
| 27171 | BAA01g19260 | A01 | 9479747 | A | C | missense_variant | MODERATE | c.113T>G|p.Leu38Arg |
S173 S265 S289 |
| 27172 | BAA01g19260 | A01 | 9479899 | C | T | upstream_gene_variant | MODIFIER | c.-40G>A| |
S155 S211 |
| 27173 | BAA01g19260 | A01 | 9482117 | C | T | upstream_gene_variant | MODIFIER | c.-2258G>A| |
S62 |
| 27174 | BAA01g19260 | A01 | 9482302 | G | A | upstream_gene_variant | MODIFIER | c.-2443C>T| |
S95 |
| 27175 | BAA01g19260 | A01 | 9482365 | G | A | upstream_gene_variant | MODIFIER | c.-2506C>T| |
S126 |