Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g62790 | A09 | 59064512 | G | A | upstream_gene_variant | MODIFIER | c.-4470G>A| |
S57 |
2 | BAA09g62790 | A09 | 59064995 | C | T | upstream_gene_variant | MODIFIER | c.-3987C>T| |
S84 |
3 | BAA09g62790 | A09 | 59065336 | C | T | upstream_gene_variant | MODIFIER | c.-3646C>T| |
S286 |
4 | BAA09g62790 | A09 | 59066561 | C | T | upstream_gene_variant | MODIFIER | c.-2421C>T| |
S153 |
5 | BAA09g62790 | A09 | 59066584 | G | A | upstream_gene_variant | MODIFIER | c.-2398G>A| |
S265 |
6 | BAA09g62790 | A09 | 59066993 | C | T | upstream_gene_variant | MODIFIER | c.-1989C>T| |
S61 |
7 | BAA09g62790 | A09 | 59068415 | G | A | upstream_gene_variant | MODIFIER | c.-567G>A| |
S38 |
8 | BAA09g62790 | A09 | 59068690 | C | T | upstream_gene_variant | MODIFIER | c.-292C>T| |
S239 |
9 | BAA09g62790 | A09 | 59069061 | G | A | missense_variant | MODERATE | c.80G>A|p.Gly27Asp |
S266 |
10 | BAA09g62790 | A09 | 59069185 | C | T | splice_region_variant&intron_variant | LOW | c.198+6C>T| |
S131 |
11 | BAA09g62790 | A09 | 59069418 | C | T | missense_variant | MODERATE | c.344C>T|p.Pro115Leu |
S279 |
12 | BAA09g62790 | A09 | 59069746 | G | A | synonymous_variant | LOW | c.672G>A|p.Arg224Arg |
S273 |
13 | BAA09g62790 | A09 | 59070641 | G | A | missense_variant | MODERATE | c.1567G>A|p.Ala523Thr |
S223 |
14 | BAA09g62790 | A09 | 59070828 | C | T | missense_variant | MODERATE | c.1754C>T|p.Ser585Phe |
S133 |
15 | BAA09g62790 | A09 | 59071220 | G | A | missense_variant | MODERATE | c.2146G>A|p.Gly716Arg |
S122 |
16 | BAA09g62790 | A09 | 59074103 | C | T | downstream_gene_variant | MODIFIER | c.*2554C>T| |
S302 |