Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g07170 | A02 | 3087622 | C | T | missense_variant | MODERATE | c.1636G>A|p.Val546Ile |
S298 |
2 | BAA02g07170 | A02 | 3088762 | C | T | missense_variant | MODERATE | c.1120G>A|p.Ala374Thr |
S276 |
3 | BAA02g07170 | A02 | 3089431 | G | A | intron_variant | MODIFIER | c.642+30C>T| |
S177 |
4 | BAA02g07170 | A02 | 3090139 | C | T | intron_variant | MODIFIER | c.298-248G>A| |
S193 |
5 | BAA02g07170 | A02 | 3091369 | G | A | upstream_gene_variant | MODIFIER | c.-497C>T| |
S192 |
6 | BAA02g07170 | A02 | 3091610 | G | A | upstream_gene_variant | MODIFIER | c.-738C>T| |
S297 |
7 | BAA02g07170 | A02 | 3091901 | G | A | upstream_gene_variant | MODIFIER | c.-1029C>T| |
S105 S106 |
8 | BAA02g07170 | A02 | 3091980 | C | T | upstream_gene_variant | MODIFIER | c.-1108G>A| |
S71 |
9 | BAA02g07170 | A02 | 3092414 | C | T | upstream_gene_variant | MODIFIER | c.-1542G>A| |
S152 |
10 | BAA02g07170 | A02 | 3092722 | C | T | upstream_gene_variant | MODIFIER | c.-1850G>A| |
S25 |
11 | BAA02g07170 | A02 | 3092818 | G | A | upstream_gene_variant | MODIFIER | c.-1946C>T| |
S197 |
12 | BAA02g07170 | A02 | 3092957 | G | A | upstream_gene_variant | MODIFIER | c.-2085C>T| |
S210 S225 |
13 | BAA02g07170 | A02 | 3093284 | G | A | upstream_gene_variant | MODIFIER | c.-2412C>T| |
S17 |
14 | BAA02g07170 | A02 | 3094029 | G | A | upstream_gene_variant | MODIFIER | c.-3157C>T| |
S148 S210 |