Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g12330 | A02 | 5545613 | C | T | upstream_gene_variant | MODIFIER | c.-4767C>T| |
S157 S163 |
2 | BAA02g12330 | A02 | 5545621 | G | A | upstream_gene_variant | MODIFIER | c.-4759G>A| |
S132 S137 S215 S89 |
3 | BAA02g12330 | A02 | 5546736 | C | T | upstream_gene_variant | MODIFIER | c.-3644C>T| |
S306 S308 |
4 | BAA02g12330 | A02 | 5546898 | G | A | upstream_gene_variant | MODIFIER | c.-3482G>A| |
S302 |
5 | BAA02g12330 | A02 | 5547749 | G | A | upstream_gene_variant | MODIFIER | c.-2631G>A| |
S45 |
6 | BAA02g12330 | A02 | 5550552 | G | A | missense_variant | MODERATE | c.173G>A|p.Gly58Glu |
S48 |
7 | BAA02g12330 | A02 | 5551194 | C | T | splice_region_variant&synonymous_variant | LOW | c.327C>T|p.Val109Val |
S299 |
8 | BAA02g12330 | A02 | 5552050 | C | T | missense_variant | MODERATE | c.946C>T|p.Arg316Cys |
S212 |
9 | BAA02g12330 | A02 | 5552992 | G | A | missense_variant&splice_region_variant | MODERATE | c.1490G>A|p.Arg497Lys |
S276 |
10 | BAA02g12330 | A02 | 5553074 | G | A | missense_variant&splice_region_variant | MODERATE | c.1492G>A|p.Val498Met |
S161 |
11 | BAA02g12330 | A02 | 5553112 | G | A | synonymous_variant | LOW | c.1530G>A|p.Glu510Glu |
S155 S211 |
12 | BAA02g12330 | A02 | 5553157 | G | A | synonymous_variant | LOW | c.1575G>A|p.Gln525Gln |
S223 |