Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g28660 | A02 | 16134757 | G | A | upstream_gene_variant | MODIFIER | c.-4704G>A| |
S148 S30 S31 |
2 | BAA02g28660 | A02 | 16134983 | C | T | upstream_gene_variant | MODIFIER | c.-4478C>T| |
S108 |
3 | BAA02g28660 | A02 | 16135032 | C | T | upstream_gene_variant | MODIFIER | c.-4429C>T| |
S162 |
4 | BAA02g28660 | A02 | 16136355 | G | A | upstream_gene_variant | MODIFIER | c.-3106G>A| |
S161 |
5 | BAA02g28660 | A02 | 16137135 | G | A | upstream_gene_variant | MODIFIER | c.-2326G>A| |
S199 |
6 | BAA02g28660 | A02 | 16137138 | G | T | upstream_gene_variant | MODIFIER | c.-2323G>T| |
S69 |
7 | BAA02g28660 | A02 | 16137789 | G | A | upstream_gene_variant | MODIFIER | c.-1672G>A| |
S173 |
8 | BAA02g28660 | A02 | 16137926 | G | A | upstream_gene_variant | MODIFIER | c.-1535G>A| |
S45 |
9 | BAA02g28660 | A02 | 16138758 | G | A | upstream_gene_variant | MODIFIER | c.-703G>A| |
S306 |
10 | BAA02g28660 | A02 | 16139022 | A | T | upstream_gene_variant | MODIFIER | c.-439A>T| |
S135 S185 S203 S273 |
11 | BAA02g28660 | A02 | 16139869 | G | A | missense_variant | MODERATE | c.325G>A|p.Ala109Thr |
S50 |
12 | BAA02g28660 | A02 | 16140711 | C | T | synonymous_variant | LOW | c.996C>T|p.His332His |
S120 |
13 | BAA02g28660 | A02 | 16142920 | G | A | downstream_gene_variant | MODIFIER | c.*2128G>A| |
S232 |
14 | BAA02g28660 | A02 | 16142973 | C | T | downstream_gene_variant | MODIFIER | c.*2181C>T| |
S283 |
15 | BAA02g28660 | A02 | 16145289 | G | A | downstream_gene_variant | MODIFIER | c.*4497G>A| |
S196 |