Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g20620 | A04 | 23665724 | C | T | upstream_gene_variant | MODIFIER | c.-2590C>T| |
S117 |
2 | BAA04g20620 | A04 | 23666382 | C | T | upstream_gene_variant | MODIFIER | c.-1932C>T| |
S265 |
3 | BAA04g20620 | A04 | 23666568 | G | A | upstream_gene_variant | MODIFIER | c.-1746G>A| |
S259 |
4 | BAA04g20620 | A04 | 23666632 | C | T | upstream_gene_variant | MODIFIER | c.-1682C>T| |
S247 |
5 | BAA04g20620 | A04 | 23666799 | C | A | upstream_gene_variant | MODIFIER | c.-1515C>A| |
S58 |
6 | BAA04g20620 | A04 | 23667815 | G | T | upstream_gene_variant | MODIFIER | c.-499G>T| |
S135 S188 S218 S23 S240 S262 S267 S5 S67 S91 |
7 | BAA04g20620 | A04 | 23670024 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.765-1G>A| |
S67 |
8 | BAA04g20620 | A04 | 23670044 | G | A | missense_variant | MODERATE | c.784G>A|p.Gly262Arg |
S293 |
9 | BAA04g20620 | A04 | 23670060 | C | T | missense_variant | MODERATE | c.800C>T|p.Pro267Leu |
S286 |
10 | BAA04g20620 | A04 | 23670555 | G | A | missense_variant | MODERATE | c.1064G>A|p.Arg355Lys |
S171 |
11 | BAA04g20620 | A04 | 23672812 | C | T | downstream_gene_variant | MODIFIER | c.*2172C>T| |
S281 |