Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g51440 | A03 | 24963361 | G | A | upstream_gene_variant | MODIFIER | c.-4589G>A| |
S267 |
2 | BAA03g51440 | A03 | 24963498 | G | A | upstream_gene_variant | MODIFIER | c.-4452G>A| |
S146 |
3 | BAA03g51440 | A03 | 24963709 | G | A | upstream_gene_variant | MODIFIER | c.-4241G>A| |
S302 |
4 | BAA03g51440 | A03 | 24965428 | G | A | upstream_gene_variant | MODIFIER | c.-2522G>A| |
S260 |
5 | BAA03g51440 | A03 | 24965585 | G | A | upstream_gene_variant | MODIFIER | c.-2365G>A| |
S132 S137 S215 S89 |
6 | BAA03g51440 | A03 | 24965680 | G | A | upstream_gene_variant | MODIFIER | c.-2270G>A| |
S56 |
7 | BAA03g51440 | A03 | 24968056 | G | A | splice_region_variant&intron_variant | LOW | c.102+5G>A| |
S48 |
8 | BAA03g51440 | A03 | 24968188 | G | A | missense_variant | MODERATE | c.157G>A|p.Ala53Thr |
S103 |
9 | BAA03g51440 | A03 | 24968986 | C | T | synonymous_variant | LOW | c.588C>T|p.Tyr196Tyr |
S140 |
10 | BAA03g51440 | A03 | 24969636 | G | A | missense_variant | MODERATE | c.1151G>A|p.Gly384Asp |
S233 |
11 | BAA03g51440 | A03 | 24970809 | G | A | synonymous_variant | LOW | c.2046G>A|p.Glu682Glu |
S242 |
12 | BAA03g51440 | A03 | 24971025 | C | T | downstream_gene_variant | MODIFIER | c.*21C>T| |
S99 |
13 | BAA03g51440 | A03 | 24971195 | C | T | downstream_gene_variant | MODIFIER | c.*191C>T| |
S142 |
14 | BAA03g51440 | A03 | 24971673 | C | T | downstream_gene_variant | MODIFIER | c.*669C>T| |
S140 |
15 | BAA03g51440 | A03 | 24971769 | C | T | downstream_gene_variant | MODIFIER | c.*765C>T| |
S18 |
16 | BAA03g51440 | A03 | 24972246 | G | A | downstream_gene_variant | MODIFIER | c.*1242G>A| |
S52 |
17 | BAA03g51440 | A03 | 24972271 | C | T | downstream_gene_variant | MODIFIER | c.*1267C>T| |
S250 |
18 | BAA03g51440 | A03 | 24973943 | G | A | downstream_gene_variant | MODIFIER | c.*2939G>A| |
S233 |