Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g66900 | A03 | 41425315 | G | A | downstream_gene_variant | MODIFIER | c.*4866C>T| |
S205 |
2 | BAA03g66900 | A03 | 41425877 | G | A | downstream_gene_variant | MODIFIER | c.*4304C>T| |
S124 |
3 | BAA03g66900 | A03 | 41426015 | G | A | downstream_gene_variant | MODIFIER | c.*4166C>T| |
S270 |
4 | BAA03g66900 | A03 | 41426097 | G | A | downstream_gene_variant | MODIFIER | c.*4084C>T| |
S182 |
5 | BAA03g66900 | A03 | 41426352 | C | T | downstream_gene_variant | MODIFIER | c.*3829G>A| |
S139 |
6 | BAA03g66900 | A03 | 41427377 | G | A | downstream_gene_variant | MODIFIER | c.*2804C>T| |
S210 |
7 | BAA03g66900 | A03 | 41430196 | G | A | synonymous_variant | LOW | c.789C>T|p.Ser263Ser |
S255 |
8 | BAA03g66900 | A03 | 41430295 | G | A | synonymous_variant | LOW | c.690C>T|p.Ile230Ile |
S238 |
9 | BAA03g66900 | A03 | 41430531 | G | A | missense_variant | MODERATE | c.454C>T|p.Leu152Phe |
S150 |
10 | BAA03g66900 | A03 | 41430572 | C | T | missense_variant | MODERATE | c.413G>A|p.Gly138Glu |
S173 |
11 | BAA03g66900 | A03 | 41432825 | C | T | upstream_gene_variant | MODIFIER | c.-1527G>A| |
S293 |
12 | BAA03g66900 | A03 | 41433246 | C | T | upstream_gene_variant | MODIFIER | c.-1948G>A| |
S205 |
13 | BAA03g66900 | A03 | 41433447 | G | A | upstream_gene_variant | MODIFIER | c.-2149C>T| |
S260 |
14 | BAA03g66900 | A03 | 41434288 | C | T | upstream_gene_variant | MODIFIER | c.-2990G>A| |
S8 |
15 | BAA03g66900 | A03 | 41434847 | C | T | upstream_gene_variant | MODIFIER | c.-3549G>A| |
S140 |
16 | BAA03g66900 | A03 | 41435660 | C | T | upstream_gene_variant | MODIFIER | c.-4362G>A| |
S176 |
17 | BAA03g66900 | A03 | 41436063 | G | A | upstream_gene_variant | MODIFIER | c.-4765C>T| |
S28 |
18 | BAA03g66900 | A03 | 41436244 | C | T | upstream_gene_variant | MODIFIER | c.-4946G>A| |
S139 |