Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g47790 | A09 | 51899998 | C | T | upstream_gene_variant | MODIFIER | c.-2347C>T| |
S94 |
2 | BAA09g47790 | A09 | 51901446 | G | A | upstream_gene_variant | MODIFIER | c.-899G>A| |
S52 |
3 | BAA09g47790 | A09 | 51902502 | G | A | missense_variant&splice_region_variant | MODERATE | c.19G>A|p.Asp7Asn |
S148 S210 |
4 | BAA09g47790 | A09 | 51903118 | C | T | synonymous_variant | LOW | c.402C>T|p.Ala134Ala |
S208 S219 |
5 | BAA09g47790 | A09 | 51904366 | G | A | splice_donor_variant&intron_variant | HIGH | c.854+1G>A| |
S167 |
6 | BAA09g47790 | A09 | 51905993 | C | T | missense_variant | MODERATE | c.1160C>T|p.Ser387Phe |
S251 |
7 | BAA09g47790 | A09 | 51906409 | G | A | missense_variant | MODERATE | c.1576G>A|p.Gly526Ser |
S56 |
8 | BAA09g47790 | A09 | 51906464 | G | A | downstream_gene_variant | MODIFIER | c.*11G>A| |
S203 |
9 | BAA09g47790 | A09 | 51908641 | G | A | downstream_gene_variant | MODIFIER | c.*2188G>A| |
S151 S263 |
10 | BAA09g47790 | A09 | 51909489 | G | A | downstream_gene_variant | MODIFIER | c.*3036G>A| |
S172 S180 S217 |
11 | BAA09g47790 | A09 | 51910842 | G | A | downstream_gene_variant | MODIFIER | c.*4389G>A| |
S74 |
12 | BAA09g47790 | A09 | 51911358 | C | T | downstream_gene_variant | MODIFIER | c.*4905C>T| |
S163 |