Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g26550 | A02 | 14837731 | C | T | downstream_gene_variant | MODIFIER | c.*3275G>A| |
S202 |
2 | BAA02g26550 | A02 | 14838207 | C | T | downstream_gene_variant | MODIFIER | c.*2799G>A| |
S25 S264 |
3 | BAA02g26550 | A02 | 14838336 | G | A | downstream_gene_variant | MODIFIER | c.*2670C>T| |
S14 |
4 | BAA02g26550 | A02 | 14838797 | C | T | downstream_gene_variant | MODIFIER | c.*2209G>A| |
S53 |
5 | BAA02g26550 | A02 | 14838802 | G | A | downstream_gene_variant | MODIFIER | c.*2204C>T| |
S143 |
6 | BAA02g26550 | A02 | 14838866 | G | A | downstream_gene_variant | MODIFIER | c.*2140C>T| |
S184 |
7 | BAA02g26550 | A02 | 14838874 | C | T | downstream_gene_variant | MODIFIER | c.*2132G>A| |
S260 |
8 | BAA02g26550 | A02 | 14838968 | G | A | downstream_gene_variant | MODIFIER | c.*2038C>T| |
S197 |
9 | BAA02g26550 | A02 | 14839853 | G | A | downstream_gene_variant | MODIFIER | c.*1153C>T| |
S155 S211 |
10 | BAA02g26550 | A02 | 14840801 | G | A | downstream_gene_variant | MODIFIER | c.*205C>T| |
S293 |
11 | BAA02g26550 | A02 | 14841210 | C | T | synonymous_variant | LOW | c.1221G>A|p.Leu407Leu |
S78 S83 |
12 | BAA02g26550 | A02 | 14841231 | G | A | synonymous_variant | LOW | c.1200C>T|p.Phe400Phe |
S239 |
13 | BAA02g26550 | A02 | 14841280 | G | A | missense_variant | MODERATE | c.1151C>T|p.Pro384Leu |
S57 |
14 | BAA02g26550 | A02 | 14841647 | C | T | missense_variant | MODERATE | c.784G>A|p.Glu262Lys |
S182 |
15 | BAA02g26550 | A02 | 14841663 | C | T | synonymous_variant | LOW | c.768G>A|p.Pro256Pro |
S181 |
16 | BAA02g26550 | A02 | 14844068 | G | A | upstream_gene_variant | MODIFIER | c.-742C>T| |
S278 |
17 | BAA02g26550 | A02 | 14846001 | C | T | upstream_gene_variant | MODIFIER | c.-2675G>A| |
S107 S234 |
18 | BAA02g26550 | A02 | 14846396 | C | T | upstream_gene_variant | MODIFIER | c.-3070G>A| |
S276 |
19 | BAA02g26550 | A02 | 14847063 | C | T | upstream_gene_variant | MODIFIER | c.-3737G>A| |
S289 S290 |