Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g50740 | A09 | 53474964 | G | A | downstream_gene_variant | MODIFIER | c.*2267C>T| |
S184 |
2 | BAA09g50740 | A09 | 53478525 | G | A | missense_variant | MODERATE | c.569C>T|p.Thr190Ile |
S266 |
3 | BAA09g50740 | A09 | 53479327 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.25-1G>A| |
S149 |
4 | BAA09g50740 | A09 | 53480649 | G | A | upstream_gene_variant | MODIFIER | c.-838C>T| |
S274 |
5 | BAA09g50740 | A09 | 53481067 | C | T | upstream_gene_variant | MODIFIER | c.-1256G>A| |
S242 |
6 | BAA09g50740 | A09 | 53483515 | C | T | upstream_gene_variant | MODIFIER | c.-3704G>A| |
S78 S83 |
7 | BAA09g50740 | A09 | 53483526 | G | T | upstream_gene_variant | MODIFIER | c.-3715C>A| |
S121 S15 S151 S182 S231 S238 S246 S259 S262 S306 S37 S63 S70 S88 |
8 | BAA09g50740 | A09 | 53483978 | G | A | upstream_gene_variant | MODIFIER | c.-4167C>T| |
S69 |
9 | BAA09g50740 | A09 | 53484180 | C | T | upstream_gene_variant | MODIFIER | c.-4369G>A| |
S60 |