Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g01870 | A08 | 1400416 | G | A | synonymous_variant | LOW | c.207C>T|p.Phe69Phe |
S119 |
2 | BAA08g01870 | A08 | 1400570 | G | A | missense_variant | MODERATE | c.53C>T|p.Thr18Ile |
S286 |
3 | BAA08g01870 | A08 | 1401355 | G | A | upstream_gene_variant | MODIFIER | c.-733C>T| |
S273 |
4 | BAA08g01870 | A08 | 1401590 | C | T | upstream_gene_variant | MODIFIER | c.-968G>A| |
S244 |
5 | BAA08g01870 | A08 | 1401695 | G | A | upstream_gene_variant | MODIFIER | c.-1073C>T| |
S128 |
6 | BAA08g01870 | A08 | 1402320 | G | A | upstream_gene_variant | MODIFIER | c.-1698C>T| |
S25 |
7 | BAA08g01870 | A08 | 1402457 | C | T | upstream_gene_variant | MODIFIER | c.-1835G>A| |
S48 |
8 | BAA08g01870 | A08 | 1405056 | G | A | upstream_gene_variant | MODIFIER | c.-4434C>T| |
S202 |
9 | BAA08g01870 | A08 | 1405526 | C | T | upstream_gene_variant | MODIFIER | c.-4904G>A| |
S189 |