Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g20170 | A02 | 10636229 | C | T | upstream_gene_variant | MODIFIER | c.-4985C>T| |
S79 |
2 | BAA02g20170 | A02 | 10636858 | C | T | upstream_gene_variant | MODIFIER | c.-4356C>T| |
S67 |
3 | BAA02g20170 | A02 | 10637158 | G | A | upstream_gene_variant | MODIFIER | c.-4056G>A| |
S272 |
4 | BAA02g20170 | A02 | 10637277 | C | T | upstream_gene_variant | MODIFIER | c.-3937C>T| |
S216 |
5 | BAA02g20170 | A02 | 10637531 | C | T | upstream_gene_variant | MODIFIER | c.-3683C>T| |
S105 S106 |
6 | BAA02g20170 | A02 | 10637558 | C | T | upstream_gene_variant | MODIFIER | c.-3656C>T| |
S165 S211 S227 |
7 | BAA02g20170 | A02 | 10640099 | G | A | upstream_gene_variant | MODIFIER | c.-1115G>A| |
S190 |
8 | BAA02g20170 | A02 | 10640546 | C | T | upstream_gene_variant | MODIFIER | c.-668C>T| |
S25 |
9 | BAA02g20170 | A02 | 10642534 | C | T | intron_variant | MODIFIER | c.801+77C>T| |
S212 |
10 | BAA02g20170 | A02 | 10644085 | C | T | intron_variant | MODIFIER | c.1329+35C>T| |
S121 |
11 | BAA02g20170 | A02 | 10648309 | G | A | synonymous_variant | LOW | c.3564G>A|p.Arg1188Arg |
S298 |
12 | BAA02g20170 | A02 | 10649639 | G | A | missense_variant | MODERATE | c.4409G>A|p.Arg1470Lys |
S155 S211 |
13 | BAA02g20170 | A02 | 10650698 | C | T | downstream_gene_variant | MODIFIER | c.*75C>T| |
S25 |
14 | BAA02g20170 | A02 | 10652158 | C | T | downstream_gene_variant | MODIFIER | c.*1535C>T| |
S185 |