Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g31180 | A01 | 20221753 | C | T | upstream_gene_variant | MODIFIER | c.-4314C>T| |
S203 S266 |
2 | BAA01g31180 | A01 | 20223806 | C | T | upstream_gene_variant | MODIFIER | c.-2261C>T| |
S69 |
3 | BAA01g31180 | A01 | 20224043 | G | A | upstream_gene_variant | MODIFIER | c.-2024G>A| |
S176 |
4 | BAA01g31180 | A01 | 20224189 | C | T | upstream_gene_variant | MODIFIER | c.-1878C>T| |
S20 |
5 | BAA01g31180 | A01 | 20224361 | G | A | upstream_gene_variant | MODIFIER | c.-1706G>A| |
S116 |
6 | BAA01g31180 | A01 | 20225508 | C | T | upstream_gene_variant | MODIFIER | c.-559C>T| |
S295 |
7 | BAA01g31180 | A01 | 20226464 | G | A | missense_variant | MODERATE | c.398G>A|p.Gly133Glu |
S23 |
8 | BAA01g31180 | A01 | 20227700 | G | A | synonymous_variant | LOW | c.1476G>A|p.Val492Val |
S169 |
9 | BAA01g31180 | A01 | 20227800 | G | A | missense_variant | MODERATE | c.1576G>A|p.Gly526Arg |
S129 |
10 | BAA01g31180 | A01 | 20228513 | C | T | intron_variant | MODIFIER | c.1597-317C>T| |
S152 |
11 | BAA01g31180 | A01 | 20228951 | C | T | missense_variant | MODERATE | c.1718C>T|p.Ser573Leu |
S205 |
12 | BAA01g31180 | A01 | 20230016 | C | T | downstream_gene_variant | MODIFIER | c.*887C>T| |
S168 |
13 | BAA01g31180 | A01 | 20230386 | C | T | downstream_gene_variant | MODIFIER | c.*1257C>T| |
S100 |
14 | BAA01g31180 | A01 | 20231307 | A | T | downstream_gene_variant | MODIFIER | c.*2178A>T| |
S121 |
15 | BAA01g31180 | A01 | 20231933 | C | T | downstream_gene_variant | MODIFIER | c.*2804C>T| |
S81 S85 |
16 | BAA01g31180 | A01 | 20233131 | A | T | downstream_gene_variant | MODIFIER | c.*4002A>T| |
S124 |
17 | BAA01g31180 | A01 | 20233402 | C | T | downstream_gene_variant | MODIFIER | c.*4273C>T| |
S213 |
18 | BAA01g31180 | A01 | 20233697 | C | T | downstream_gene_variant | MODIFIER | c.*4568C>T| |
S127 |