| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 185051 | BAA02g22890 | A02 | 12429432 | G | A | downstream_gene_variant | MODIFIER | c.*1490C>T| |
S17 |
| 185052 | BAA02g22900 | A02 | 12430657 | G | A | upstream_gene_variant | MODIFIER | c.-4086G>A| |
S190 |
| 185053 | BAA02g22900 | A02 | 12430880 | G | A | upstream_gene_variant | MODIFIER | c.-3863G>A| |
S107 |
| 185054 | BAA02g22890 | A02 | 12430934 | C | T | stop_gained | HIGH | c.159G>A|p.Trp53* |
S76 |
| 185055 | BAA02g22890 | A02 | 12431098 | C | T | upstream_gene_variant | MODIFIER | c.-6G>A| |
S94 |
| 185056 | BAA02g22890 | A02 | 12431746 | G | A | upstream_gene_variant | MODIFIER | c.-654C>T| |
S12 |
| 185057 | BAA02g22890 | A02 | 12433044 | G | A | upstream_gene_variant | MODIFIER | c.-1952C>T| |
S274 |
| 185058 | BAA02g22890 | A02 | 12433174 | G | A | upstream_gene_variant | MODIFIER | c.-2082C>T| |
S256 |
| 185059 | BAA02g22890 | A02 | 12433611 | G | A | upstream_gene_variant | MODIFIER | c.-2519C>T| |
S238 |
| 185060 | BAA02g22890 | A02 | 12433906 | G | A | upstream_gene_variant | MODIFIER | c.-2814C>T| |
S288 |
| 185061 | BAA02g22890 | A02 | 12434183 | G | A | upstream_gene_variant | MODIFIER | c.-3091C>T| |
S74 |
| 185062 | BAA02g22890 | A02 | 12434271 | G | A | upstream_gene_variant | MODIFIER | c.-3179C>T| |
S155 S211 |
| 185063 | BAA02g22890 | A02 | 12434280 | C | T | upstream_gene_variant | MODIFIER | c.-3188G>A| |
S224 |
| 185064 | BAA02g22890 | A02 | 12434345 | G | A | upstream_gene_variant | MODIFIER | c.-3253C>T| |
S291 |
| 185065 | BAA02g22890 | A02 | 12434412 | G | A | upstream_gene_variant | MODIFIER | c.-3320C>T| |
S72 |
| 185066 | BAA02g22900 | A02 | 12434875 | C | T | missense_variant | MODERATE | c.133C>T|p.Pro45Ser |
S159 S188 S243 S276 S298 S299 |
| 185067 | BAA02g22900 | A02 | 12435566 | C | T | missense_variant | MODERATE | c.482C>T|p.Ser161Leu |
S224 |
| 185068 | BAA02g22900 | A02 | 12436396 | G | A | missense_variant&splice_region_variant | MODERATE | c.854G>A|p.Gly285Glu |
S295 |
| 185069 | BAA02g22910 | A02 | 12438778 | C | T | upstream_gene_variant | MODIFIER | c.-2668C>T| |
S233 |
| 185070 | BAA02g22910 | A02 | 12441630 | C | T | missense_variant | MODERATE | c.185C>T|p.Ser62Phe |
S87 |
| 185071 | BAA02g22910 | A02 | 12441896 | C | T | missense_variant | MODERATE | c.451C>T|p.Pro151Ser |
S158 |
| 185072 | BAA02g22920 | A02 | 12443355 | G | A | downstream_gene_variant | MODIFIER | c.*5000C>T| |
S306 |
| 185073 | BAA02g22920 | A02 | 12446214 | G | A | downstream_gene_variant | MODIFIER | c.*2141C>T| |
S288 |
| 185074 | BAA02g22920 | A02 | 12446216 | G | A | downstream_gene_variant | MODIFIER | c.*2139C>T| |
S43 |
| 185075 | BAA02g22920 | A02 | 12446903 | C | T | downstream_gene_variant | MODIFIER | c.*1452G>A| |
S77 S82 |