Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g46120 | A02 | 37582424 | C | T | upstream_gene_variant | MODIFIER | c.-4990C>T| |
S284 |
2 | BAA02g46120 | A02 | 37582994 | C | T | upstream_gene_variant | MODIFIER | c.-4420C>T| |
S175 |
3 | BAA02g46120 | A02 | 37583600 | G | A | upstream_gene_variant | MODIFIER | c.-3814G>A| |
S30 S4 |
4 | BAA02g46120 | A02 | 37583816 | A | T | upstream_gene_variant | MODIFIER | c.-3598A>T| |
S286 |
5 | BAA02g46120 | A02 | 37583970 | G | A | upstream_gene_variant | MODIFIER | c.-3444G>A| |
S155 S211 |
6 | BAA02g46120 | A02 | 37584146 | C | T | upstream_gene_variant | MODIFIER | c.-3268C>T| |
S173 |
7 | BAA02g46120 | A02 | 37584575 | G | A | upstream_gene_variant | MODIFIER | c.-2839G>A| |
S308 |
8 | BAA02g46120 | A02 | 37585802 | G | A | upstream_gene_variant | MODIFIER | c.-1612G>A| |
S152 |
9 | BAA02g46120 | A02 | 37585954 | G | A | upstream_gene_variant | MODIFIER | c.-1460G>A| |
S19 |
10 | BAA02g46120 | A02 | 37586237 | G | A | upstream_gene_variant | MODIFIER | c.-1177G>A| |
S166 |
11 | BAA02g46120 | A02 | 37587444 | G | A | missense_variant | MODERATE | c.31G>A|p.Asp11Asn |
S238 |
12 | BAA02g46120 | A02 | 37587508 | G | A | missense_variant | MODERATE | c.95G>A|p.Cys32Tyr |
S20 |
13 | BAA02g46120 | A02 | 37588945 | C | T | downstream_gene_variant | MODIFIER | c.*209C>T| |
S283 |
14 | BAA02g46120 | A02 | 37589285 | C | T | downstream_gene_variant | MODIFIER | c.*549C>T| |
S3 |
15 | BAA02g46120 | A02 | 37590715 | C | T | downstream_gene_variant | MODIFIER | c.*1979C>T| |
S6 |
16 | BAA02g46120 | A02 | 37590902 | C | T | downstream_gene_variant | MODIFIER | c.*2166C>T| |
S42 |