Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g10150 | A02 | 4493631 | C | T | downstream_gene_variant | MODIFIER | c.*2301G>A| |
S270 |
2 | BAA02g10150 | A02 | 4494136 | C | T | downstream_gene_variant | MODIFIER | c.*1796G>A| |
S138 |
3 | BAA02g10150 | A02 | 4494453 | C | T | downstream_gene_variant | MODIFIER | c.*1479G>A| |
S121 |
4 | BAA02g10150 | A02 | 4494698 | G | A | downstream_gene_variant | MODIFIER | c.*1234C>T| |
S169 |
5 | BAA02g10150 | A02 | 4494735 | C | T | downstream_gene_variant | MODIFIER | c.*1197G>A| |
S267 |
6 | BAA02g10150 | A02 | 4494827 | C | T | downstream_gene_variant | MODIFIER | c.*1105G>A| |
S257 |
7 | BAA02g10150 | A02 | 4494872 | C | T | downstream_gene_variant | MODIFIER | c.*1060G>A| |
S135 |
8 | BAA02g10150 | A02 | 4494960 | C | T | downstream_gene_variant | MODIFIER | c.*972G>A| |
S157 |
9 | BAA02g10150 | A02 | 4496534 | C | T | splice_donor_variant&intron_variant | HIGH | c.833+1G>A| |
S65 S67 |
10 | BAA02g10150 | A02 | 4496849 | G | A | synonymous_variant | LOW | c.519C>T|p.Tyr173Tyr |
S173 |
11 | BAA02g10150 | A02 | 4497923 | C | T | upstream_gene_variant | MODIFIER | c.-556G>A| |
S216 |
12 | BAA02g10150 | A02 | 4498183 | C | T | upstream_gene_variant | MODIFIER | c.-816G>A| |
S234 |
13 | BAA02g10150 | A02 | 4498389 | C | T | upstream_gene_variant | MODIFIER | c.-1022G>A| |
S58 |
14 | BAA02g10150 | A02 | 4499913 | G | A | upstream_gene_variant | MODIFIER | c.-2546C>T| |
S23 |
15 | BAA02g10150 | A02 | 4501547 | C | T | upstream_gene_variant | MODIFIER | c.-4180G>A| |
S178 |
16 | BAA02g10150 | A02 | 4502167 | G | A | upstream_gene_variant | MODIFIER | c.-4800C>T| |
S173 |