Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g02850 | A04 | 1698831 | C | T | missense_variant | MODERATE | c.631G>A|p.Asp211Asn |
S202 |
2 | BAA04g02850 | A04 | 1700558 | C | T | upstream_gene_variant | MODIFIER | c.-666G>A| |
S247 |
3 | BAA04g02850 | A04 | 1701361 | C | T | upstream_gene_variant | MODIFIER | c.-1469G>A| |
S4 |
4 | BAA04g02850 | A04 | 1701569 | C | T | upstream_gene_variant | MODIFIER | c.-1677G>A| |
S209 |
5 | BAA04g02850 | A04 | 1702462 | C | T | upstream_gene_variant | MODIFIER | c.-2570G>A| |
S296 |
6 | BAA04g02850 | A04 | 1703165 | C | T | upstream_gene_variant | MODIFIER | c.-3273G>A| |
S152 |
7 | BAA04g02850 | A04 | 1703344 | C | T | upstream_gene_variant | MODIFIER | c.-3452G>A| |
S82 S92 |
8 | BAA04g02850 | A04 | 1703440 | G | A | upstream_gene_variant | MODIFIER | c.-3548C>T| |
S133 |
9 | BAA04g02850 | A04 | 1703743 | G | A | upstream_gene_variant | MODIFIER | c.-3851C>T| |
S298 |
10 | BAA04g02850 | A04 | 1704167 | G | A | upstream_gene_variant | MODIFIER | c.-4275C>T| |
S17 |
11 | BAA04g02850 | A04 | 1704510 | C | T | upstream_gene_variant | MODIFIER | c.-4618G>A| |
S43 |