Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g09660 | A02 | 4247686 | C | T | downstream_gene_variant | MODIFIER | c.*1161G>A| |
S266 |
2 | BAA02g09660 | A02 | 4248864 | G | A | missense_variant | MODERATE | c.415C>T|p.Pro139Ser |
S239 |
3 | BAA02g09660 | A02 | 4249222 | C | T | stop_gained | HIGH | c.57G>A|p.Trp19* |
S42 |
4 | BAA02g09660 | A02 | 4249813 | G | A | upstream_gene_variant | MODIFIER | c.-535C>T| |
S279 |
5 | BAA02g09660 | A02 | 4251552 | C | T | upstream_gene_variant | MODIFIER | c.-2274G>A| |
S226 |
6 | BAA02g09660 | A02 | 4251652 | C | T | upstream_gene_variant | MODIFIER | c.-2374G>A| |
S262 |
7 | BAA02g09660 | A02 | 4251688 | G | A | upstream_gene_variant | MODIFIER | c.-2410C>T| |
S12 |
8 | BAA02g09660 | A02 | 4251983 | G | A | upstream_gene_variant | MODIFIER | c.-2705C>T| |
S122 |
9 | BAA02g09660 | A02 | 4252577 | C | T | upstream_gene_variant | MODIFIER | c.-3299G>A| |
S8 |
10 | BAA02g09660 | A02 | 4253409 | G | A | upstream_gene_variant | MODIFIER | c.-4131C>T| |
S264 |