Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g26690 | A09 | 17378358 | G | A | upstream_gene_variant | MODIFIER | c.-3327G>A| |
S295 |
2 | BAA09g26690 | A09 | 17378458 | C | T | upstream_gene_variant | MODIFIER | c.-3227C>T| |
S286 |
3 | BAA09g26690 | A09 | 17378821 | G | A | upstream_gene_variant | MODIFIER | c.-2864G>A| |
S189 |
4 | BAA09g26690 | A09 | 17378937 | C | T | upstream_gene_variant | MODIFIER | c.-2748C>T| |
S289 S290 |
5 | BAA09g26690 | A09 | 17379027 | G | A | upstream_gene_variant | MODIFIER | c.-2658G>A| |
S292 |
6 | BAA09g26690 | A09 | 17379338 | C | T | upstream_gene_variant | MODIFIER | c.-2347C>T| |
S193 |
7 | BAA09g26690 | A09 | 17379410 | C | T | upstream_gene_variant | MODIFIER | c.-2275C>T| |
S133 |
8 | BAA09g26690 | A09 | 17380013 | C | T | upstream_gene_variant | MODIFIER | c.-1672C>T| |
S282 |
9 | BAA09g26690 | A09 | 17381840 | C | T | synonymous_variant | LOW | c.156C>T|p.Leu52Leu |
S174 |
10 | BAA09g26690 | A09 | 17382108 | G | A | missense_variant | MODERATE | c.424G>A|p.Gly142Arg |
S249 |
11 | BAA09g26690 | A09 | 17382424 | C | T | missense_variant | MODERATE | c.740C>T|p.Thr247Met |
S143 |
12 | BAA09g26690 | A09 | 17382756 | C | T | stop_gained | HIGH | c.1072C>T|p.Gln358* |
S18 |
13 | BAA09g26690 | A09 | 17382803 | G | A | synonymous_variant | LOW | c.1119G>A|p.Leu373Leu |
S167 |
14 | BAA09g26690 | A09 | 17383182 | G | A | missense_variant | MODERATE | c.1498G>A|p.Glu500Lys |
S165 |