Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g31120 | A02 | 18472288 | G | A | upstream_gene_variant | MODIFIER | c.-4488G>A| |
S7 |
2 | BAA02g31120 | A02 | 18472480 | C | T | upstream_gene_variant | MODIFIER | c.-4296C>T| |
S189 |
3 | BAA02g31120 | A02 | 18473532 | G | A | upstream_gene_variant | MODIFIER | c.-3244G>A| |
S111 |
4 | BAA02g31120 | A02 | 18473637 | C | T | upstream_gene_variant | MODIFIER | c.-3139C>T| |
S52 |
5 | BAA02g31120 | A02 | 18474299 | C | T | upstream_gene_variant | MODIFIER | c.-2477C>T| |
S245 |
6 | BAA02g31120 | A02 | 18475971 | C | T | upstream_gene_variant | MODIFIER | c.-805C>T| |
S240 |
7 | BAA02g31120 | A02 | 18476595 | C | T | upstream_gene_variant | MODIFIER | c.-181C>T| |
S234 |
8 | BAA02g31120 | A02 | 18476877 | G | A | synonymous_variant | LOW | c.102G>A|p.Glu34Glu |
S271 |
9 | BAA02g31120 | A02 | 18478942 | G | A | missense_variant | MODERATE | c.922G>A|p.Asp308Asn |
S291 |
10 | BAA02g31120 | A02 | 18479317 | G | A | missense_variant | MODERATE | c.1297G>A|p.Glu433Lys |
S298 |
11 | BAA02g31120 | A02 | 18479319 | G | A | synonymous_variant | LOW | c.1299G>A|p.Glu433Glu |
S20 |
12 | BAA02g31120 | A02 | 18479370 | G | A | synonymous_variant | LOW | c.1350G>A|p.Lys450Lys |
S230 |
13 | BAA02g31120 | A02 | 18480960 | G | A | downstream_gene_variant | MODIFIER | c.*1554G>A| |
S47 |
14 | BAA02g31120 | A02 | 18481263 | C | T | downstream_gene_variant | MODIFIER | c.*1857C>T| |
S138 |