Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g28020 | A09 | 18401331 | C | T | upstream_gene_variant | MODIFIER | c.-4812C>T| |
S159 S243 S299 |
2 | BAA09g28020 | A09 | 18403311 | G | A | upstream_gene_variant | MODIFIER | c.-2832G>A| |
S77 S82 |
3 | BAA09g28020 | A09 | 18407727 | G | A | missense_variant | MODERATE | c.182G>A|p.Gly61Asp |
S232 |
4 | BAA09g28020 | A09 | 18408660 | G | A | missense_variant&splice_region_variant | MODERATE | c.445G>A|p.Val149Ile |
S202 |
5 | BAA09g28020 | A09 | 18408988 | C | T | missense_variant | MODERATE | c.686C>T|p.Ala229Val |
S206 S26 |
6 | BAA09g28020 | A09 | 18409027 | T | C | missense_variant | MODERATE | c.725T>C|p.Leu242Pro |
S298 |
7 | BAA09g28020 | A09 | 18410613 | G | A | downstream_gene_variant | MODIFIER | c.*1432G>A| |
S116 |
8 | BAA09g28020 | A09 | 18412217 | C | T | downstream_gene_variant | MODIFIER | c.*3036C>T| |
S269 |
9 | BAA09g28020 | A09 | 18413762 | C | T | downstream_gene_variant | MODIFIER | c.*4581C>T| |
S219 |
10 | BAA09g28020 | A09 | 18414133 | G | A | downstream_gene_variant | MODIFIER | c.*4952G>A| |
S238 |