| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 180151 | BAA02g20240 | A02 | 10673855 | C | T | upstream_gene_variant | MODIFIER | c.-1614C>T| |
S160 |
| 180152 | BAA02g20240 | A02 | 10674544 | C | T | upstream_gene_variant | MODIFIER | c.-925C>T| |
S25 |
| 180153 | BAA02g20240 | A02 | 10675688 | G | A | missense_variant | MODERATE | c.220G>A|p.Val74Ile |
S37 |
| 180154 | BAA02g20240 | A02 | 10675716 | G | A | missense_variant | MODERATE | c.248G>A|p.Ser83Asn |
S4 |
| 180155 | BAA02g20240 | A02 | 10675773 | C | T | missense_variant | MODERATE | c.305C>T|p.Ser102Phe |
S134 |
| 180156 | BAA02g20240 | A02 | 10676321 | C | T | missense_variant | MODERATE | c.775C>T|p.Pro259Ser |
S164 |
| 180157 | BAA02g20240 | A02 | 10676974 | C | T | stop_gained | HIGH | c.1165C>T|p.Gln389* |
S65 |
| 180158 | BAA02g20240 | A02 | 10678518 | G | A | downstream_gene_variant | MODIFIER | c.*1110G>A| |
S144 |
| 180159 | BAA02g20240 | A02 | 10679112 | G | A | downstream_gene_variant | MODIFIER | c.*1704G>A| |
S150 |
| 180160 | BAA02g20250 | A02 | 10681648 | C | T | upstream_gene_variant | MODIFIER | c.-2168G>A| |
S138 |
| 180161 | BAA02g20250 | A02 | 10683274 | C | T | upstream_gene_variant | MODIFIER | c.-3794G>A| |
S195 |
| 180162 | BAA02g20250 | A02 | 10683404 | C | T | upstream_gene_variant | MODIFIER | c.-3924G>A| |
S5 |
| 180163 | BAA02g20250 | A02 | 10684391 | C | T | upstream_gene_variant | MODIFIER | c.-4911G>A| |
S185 |
| 180164 | BAA02g20260 | A02 | 10685806 | G | A | upstream_gene_variant | MODIFIER | c.-443C>T| |
S172 S217 |
| 180165 | BAA02g20270 | A02 | 10686474 | G | A | missense_variant | MODERATE | c.8G>A|p.Arg3Lys |
S279 |
| 180166 | BAA02g20270 | A02 | 10686562 | C | T | synonymous_variant | LOW | c.96C>T|p.Ser32Ser |
S302 |
| 180167 | BAA02g20270 | A02 | 10686754 | C | T | synonymous_variant | LOW | c.288C>T|p.Val96Val |
S108 |
| 180168 | BAA02g20270 | A02 | 10687602 | G | A | missense_variant | MODERATE | c.1136G>A|p.Arg379Lys |
S291 |
| 180169 | BAA02g20260 | A02 | 10688790 | C | T | upstream_gene_variant | MODIFIER | c.-3427G>A| |
S167 |
| 180170 | BAA02g20260 | A02 | 10688859 | C | T | upstream_gene_variant | MODIFIER | c.-3496G>A| |
S301 S304 |
| 180171 | BAA02g20260 | A02 | 10688863 | G | A | upstream_gene_variant | MODIFIER | c.-3500C>T| |
S297 |
| 180172 | BAA02g20280 | A02 | 10690497 | G | A | missense_variant | MODERATE | c.439G>A|p.Glu147Lys |
S43 |
| 180173 | BAA02g20290 | A02 | 10691721 | C | T | missense_variant | MODERATE | c.910G>A|p.Asp304Asn |
S1 S90 |
| 180174 | BAA02g20270 | A02 | 10692067 | C | T | downstream_gene_variant | MODIFIER | c.*3750C>T| |
S6 |
| 180175 | BAA02g20290 | A02 | 10692890 | C | T | missense_variant | MODERATE | c.454G>A|p.Glu152Lys |
S255 |