Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g19100 | A02 | 9896196 | G | A | downstream_gene_variant | MODIFIER | c.*1727C>T| |
S79 S91 |
2 | BAA02g19100 | A02 | 9896232 | C | T | downstream_gene_variant | MODIFIER | c.*1691G>A| |
S183 S198 |
3 | BAA02g19100 | A02 | 9896367 | G | A | downstream_gene_variant | MODIFIER | c.*1556C>T| |
S137 S215 |
4 | BAA02g19100 | A02 | 9896471 | C | T | downstream_gene_variant | MODIFIER | c.*1452G>A| |
S2 |
5 | BAA02g19100 | A02 | 9898318 | C | T | missense_variant | MODERATE | c.208G>A|p.Ala70Thr |
S302 |
6 | BAA02g19100 | A02 | 9899785 | C | T | upstream_gene_variant | MODIFIER | c.-1260G>A| |
S32 |
7 | BAA02g19100 | A02 | 9900135 | G | A | upstream_gene_variant | MODIFIER | c.-1610C>T| |
S293 |
8 | BAA02g19100 | A02 | 9900771 | G | A | upstream_gene_variant | MODIFIER | c.-2246C>T| |
S86 |
9 | BAA02g19100 | A02 | 9900780 | G | A | upstream_gene_variant | MODIFIER | c.-2255C>T| |
S295 |
10 | BAA02g19100 | A02 | 9901268 | C | T | upstream_gene_variant | MODIFIER | c.-2743G>A| |
S216 S241 S265 S39 |
11 | BAA02g19100 | A02 | 9902209 | C | T | upstream_gene_variant | MODIFIER | c.-3684G>A| |
S165 |
12 | BAA02g19100 | A02 | 9902541 | G | A | upstream_gene_variant | MODIFIER | c.-4016C>T| |
S4 |
13 | BAA02g19100 | A02 | 9902926 | G | A | upstream_gene_variant | MODIFIER | c.-4401C>T| |
S269 |
14 | BAA02g19100 | A02 | 9903156 | C | T | upstream_gene_variant | MODIFIER | c.-4631G>A| |
S270 |
15 | BAA02g19100 | A02 | 9903184 | C | T | upstream_gene_variant | MODIFIER | c.-4659G>A| |
S131 |