Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g15700 | A05 | 8424289 | C | T | upstream_gene_variant | MODIFIER | c.-4328C>T| |
S228 |
2 | BAA05g15700 | A05 | 8424420 | C | T | upstream_gene_variant | MODIFIER | c.-4197C>T| |
S267 |
3 | BAA05g15700 | A05 | 8424759 | C | T | upstream_gene_variant | MODIFIER | c.-3858C>T| |
S143 |
4 | BAA05g15700 | A05 | 8425185 | C | T | upstream_gene_variant | MODIFIER | c.-3432C>T| |
S246 |
5 | BAA05g15700 | A05 | 8425293 | C | T | upstream_gene_variant | MODIFIER | c.-3324C>T| |
S57 |
6 | BAA05g15700 | A05 | 8425307 | C | T | upstream_gene_variant | MODIFIER | c.-3310C>T| |
S35 |
7 | BAA05g15700 | A05 | 8426270 | C | T | upstream_gene_variant | MODIFIER | c.-2347C>T| |
S188 |
8 | BAA05g15700 | A05 | 8426346 | G | A | upstream_gene_variant | MODIFIER | c.-2271G>A| |
S203 |
9 | BAA05g15700 | A05 | 8428114 | C | T | upstream_gene_variant | MODIFIER | c.-503C>T| |
S17 |
10 | BAA05g15700 | A05 | 8428813 | C | T | intron_variant | MODIFIER | c.57+140C>T| |
S280 |
11 | BAA05g15700 | A05 | 8429639 | C | T | missense_variant | MODERATE | c.355C>T|p.Pro119Ser |
S146 |
12 | BAA05g15700 | A05 | 8429674 | C | T | synonymous_variant | LOW | c.390C>T|p.Tyr130Tyr |
S266 |
13 | BAA05g15700 | A05 | 8430393 | C | T | downstream_gene_variant | MODIFIER | c.*58C>T| |
S183 S198 |
14 | BAA05g15700 | A05 | 8431381 | C | T | downstream_gene_variant | MODIFIER | c.*1046C>T| |
S72 S78 |
15 | BAA05g15700 | A05 | 8432667 | G | A | downstream_gene_variant | MODIFIER | c.*2332G>A| |
S161 |
16 | BAA05g15700 | A05 | 8432683 | C | T | downstream_gene_variant | MODIFIER | c.*2348C>T| |
S262 |
17 | BAA05g15700 | A05 | 8434011 | G | A | downstream_gene_variant | MODIFIER | c.*3676G>A| |
S247 |
18 | BAA05g15700 | A05 | 8435023 | G | A | downstream_gene_variant | MODIFIER | c.*4688G>A| |
S11 |
19 | BAA05g15700 | A05 | 8435053 | C | T | downstream_gene_variant | MODIFIER | c.*4718C>T| |
S286 |