Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g10300 | A04 | 16471919 | C | T | missense_variant | MODERATE | c.1450G>A|p.Ala484Thr |
S135 |
2 | BAA04g10300 | A04 | 16471951 | C | T | missense_variant | MODERATE | c.1418G>A|p.Arg473Lys |
S293 |
3 | BAA04g10300 | A04 | 16472306 | G | A | missense_variant | MODERATE | c.1063C>T|p.Pro355Ser |
S295 |
4 | BAA04g10300 | A04 | 16472570 | C | T | synonymous_variant | LOW | c.927G>A|p.Arg309Arg |
S247 |
5 | BAA04g10300 | A04 | 16472838 | G | A | missense_variant | MODERATE | c.659C>T|p.Pro220Leu |
S38 |
6 | BAA04g10300 | A04 | 16473068 | G | A | synonymous_variant | LOW | c.429C>T|p.Arg143Arg |
S162 |
7 | BAA04g10300 | A04 | 16475316 | C | T | upstream_gene_variant | MODIFIER | c.-1820G>A| |
S268 |
8 | BAA04g10300 | A04 | 16475568 | G | A | upstream_gene_variant | MODIFIER | c.-2072C>T| |
S69 |
9 | BAA04g10300 | A04 | 16476514 | G | A | upstream_gene_variant | MODIFIER | c.-3018C>T| |
S126 |
10 | BAA04g10300 | A04 | 16476558 | G | A | upstream_gene_variant | MODIFIER | c.-3062C>T| |
S261 |
11 | BAA04g10300 | A04 | 16476929 | C | T | upstream_gene_variant | MODIFIER | c.-3433G>A| |
S176 |
12 | BAA04g10300 | A04 | 16477034 | G | A | upstream_gene_variant | MODIFIER | c.-3538C>T| |
S69 |