Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g03390 | A04 | 2078377 | C | T | missense_variant | MODERATE | c.694G>A|p.Ala232Thr |
S202 |
2 | BAA04g03390 | A04 | 2079436 | C | T | synonymous_variant | LOW | c.18G>A|p.Val6Val |
S20 |
3 | BAA04g03390 | A04 | 2080325 | G | A | upstream_gene_variant | MODIFIER | c.-872C>T| |
S36 |
4 | BAA04g03390 | A04 | 2080329 | G | A | upstream_gene_variant | MODIFIER | c.-876C>T| |
S229 |
5 | BAA04g03390 | A04 | 2080606 | C | T | upstream_gene_variant | MODIFIER | c.-1153G>A| |
S80 |
6 | BAA04g03390 | A04 | 2080730 | C | T | upstream_gene_variant | MODIFIER | c.-1277G>A| |
S107 |
7 | BAA04g03390 | A04 | 2080804 | G | A | upstream_gene_variant | MODIFIER | c.-1351C>T| |
S244 |
8 | BAA04g03390 | A04 | 2081615 | C | T | upstream_gene_variant | MODIFIER | c.-2162G>A| |
S20 |
9 | BAA04g03390 | A04 | 2082264 | G | A | upstream_gene_variant | MODIFIER | c.-2811C>T| |
S36 |
10 | BAA04g03390 | A04 | 2082390 | C | T | upstream_gene_variant | MODIFIER | c.-2937G>A| |
S283 |
11 | BAA04g03390 | A04 | 2083216 | C | T | upstream_gene_variant | MODIFIER | c.-3763G>A| |
S274 |
12 | BAA04g03390 | A04 | 2083615 | G | A | upstream_gene_variant | MODIFIER | c.-4162C>T| |
S112 |
13 | BAA04g03390 | A04 | 2083885 | G | A | upstream_gene_variant | MODIFIER | c.-4432C>T| |
S170 |