Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g16160 | A04 | 20664580 | C | T | missense_variant | MODERATE | c.413G>A|p.Gly138Glu |
S43 |
2 | BAA04g16160 | A04 | 20665057 | G | A | upstream_gene_variant | MODIFIER | c.-65C>T| |
S284 |
3 | BAA04g16160 | A04 | 20665476 | C | T | upstream_gene_variant | MODIFIER | c.-484G>A| |
S306 |
4 | BAA04g16160 | A04 | 20667370 | G | A | upstream_gene_variant | MODIFIER | c.-2378C>T| |
S59 |
5 | BAA04g16160 | A04 | 20667635 | C | T | upstream_gene_variant | MODIFIER | c.-2643G>A| |
S117 |
6 | BAA04g16160 | A04 | 20667812 | C | T | upstream_gene_variant | MODIFIER | c.-2820G>A| |
S65 |
7 | BAA04g16160 | A04 | 20667969 | C | T | upstream_gene_variant | MODIFIER | c.-2977G>A| |
S200 |
8 | BAA04g16160 | A04 | 20668796 | G | A | upstream_gene_variant | MODIFIER | c.-3804C>T| |
S69 |
9 | BAA04g16160 | A04 | 20668895 | C | T | upstream_gene_variant | MODIFIER | c.-3903G>A| |
S81 S85 |
10 | BAA04g16160 | A04 | 20669297 | G | A | upstream_gene_variant | MODIFIER | c.-4305C>T| |
S57 |
11 | BAA04g16160 | A04 | 20669377 | C | T | upstream_gene_variant | MODIFIER | c.-4385G>A| |
S74 |