Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g25700 | A05 | 30490284 | G | A | upstream_gene_variant | MODIFIER | c.-4166G>A| |
S77 S82 |
2 | BAA05g25700 | A05 | 30490452 | G | A | upstream_gene_variant | MODIFIER | c.-3998G>A| |
S249 |
3 | BAA05g25700 | A05 | 30490488 | G | A | upstream_gene_variant | MODIFIER | c.-3962G>A| |
S279 |
4 | BAA05g25700 | A05 | 30490847 | G | A | upstream_gene_variant | MODIFIER | c.-3603G>A| |
S152 |
5 | BAA05g25700 | A05 | 30490990 | G | A | upstream_gene_variant | MODIFIER | c.-3460G>A| |
S104 S52 |
6 | BAA05g25700 | A05 | 30491319 | G | A | upstream_gene_variant | MODIFIER | c.-3131G>A| |
S259 |
7 | BAA05g25700 | A05 | 30491371 | C | T | upstream_gene_variant | MODIFIER | c.-3079C>T| |
S116 |
8 | BAA05g25700 | A05 | 30491649 | C | T | upstream_gene_variant | MODIFIER | c.-2801C>T| |
S137 S215 |
9 | BAA05g25700 | A05 | 30494031 | G | A | upstream_gene_variant | MODIFIER | c.-419G>A| |
S136 |
10 | BAA05g25700 | A05 | 30494904 | C | T | missense_variant | MODERATE | c.244C>T|p.Leu82Phe |
S2 |
11 | BAA05g25700 | A05 | 30495101 | C | T | intron_variant | MODIFIER | c.336+105C>T| |
S174 |
12 | BAA05g25700 | A05 | 30495854 | C | T | missense_variant | MODERATE | c.647C>T|p.Ser216Phe |
S208 S93 |