Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g39850 | A02 | 33738891 | G | A | downstream_gene_variant | MODIFIER | c.*4169C>T| |
S256 |
2 | BAA02g39850 | A02 | 33739095 | G | A | downstream_gene_variant | MODIFIER | c.*3965C>T| |
S264 |
3 | BAA02g39850 | A02 | 33739207 | C | T | downstream_gene_variant | MODIFIER | c.*3853G>A| |
S250 |
4 | BAA02g39850 | A02 | 33739552 | C | T | downstream_gene_variant | MODIFIER | c.*3508G>A| |
S64 |
5 | BAA02g39850 | A02 | 33740154 | C | T | downstream_gene_variant | MODIFIER | c.*2906G>A| |
S18 |
6 | BAA02g39850 | A02 | 33740518 | G | A | downstream_gene_variant | MODIFIER | c.*2542C>T| |
S36 |
7 | BAA02g39850 | A02 | 33740842 | C | T | downstream_gene_variant | MODIFIER | c.*2218G>A| |
S174 |
8 | BAA02g39850 | A02 | 33740956 | G | A | downstream_gene_variant | MODIFIER | c.*2104C>T| |
S177 |
9 | BAA02g39850 | A02 | 33741145 | C | T | downstream_gene_variant | MODIFIER | c.*1915G>A| |
S140 |
10 | BAA02g39850 | A02 | 33741738 | G | A | downstream_gene_variant | MODIFIER | c.*1322C>T| |
S268 |
11 | BAA02g39850 | A02 | 33743086 | G | A | missense_variant | MODERATE | c.496C>T|p.Pro166Ser |
S168 |
12 | BAA02g39850 | A02 | 33743187 | G | A | intron_variant | MODIFIER | c.427-32C>T| |
S129 |
13 | BAA02g39850 | A02 | 33744185 | C | T | missense_variant | MODERATE | c.100G>A|p.Gly34Arg |
S181 |
14 | BAA02g39850 | A02 | 33745046 | C | T | upstream_gene_variant | MODIFIER | c.-502G>A| |
S108 |
15 | BAA02g39850 | A02 | 33745445 | G | A | upstream_gene_variant | MODIFIER | c.-901C>T| |
S11 |
16 | BAA02g39850 | A02 | 33745959 | C | T | upstream_gene_variant | MODIFIER | c.-1415G>A| |
S241 |
17 | BAA02g39850 | A02 | 33747548 | C | T | upstream_gene_variant | MODIFIER | c.-3004G>A| |
S185 |
18 | BAA02g39850 | A02 | 33748804 | C | T | upstream_gene_variant | MODIFIER | c.-4260G>A| |
S242 |
19 | BAA02g39850 | A02 | 33748815 | G | A | upstream_gene_variant | MODIFIER | c.-4271C>T| |
S246 |
20 | BAA02g39850 | A02 | 33749279 | G | A | upstream_gene_variant | MODIFIER | c.-4735C>T| |
S295 |