Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g44310 | A02 | 36541203 | G | A | upstream_gene_variant | MODIFIER | c.-4911G>A| |
S232 |
2 | BAA02g44310 | A02 | 36541631 | G | A | upstream_gene_variant | MODIFIER | c.-4483G>A| |
S291 |
3 | BAA02g44310 | A02 | 36541673 | C | T | upstream_gene_variant | MODIFIER | c.-4441C>T| |
S17 |
4 | BAA02g44310 | A02 | 36541873 | A | G | upstream_gene_variant | MODIFIER | c.-4241A>G| |
S111 |
5 | BAA02g44310 | A02 | 36541890 | T | C | upstream_gene_variant | MODIFIER | c.-4224T>C| |
S111 |
6 | BAA02g44310 | A02 | 36542545 | G | A | upstream_gene_variant | MODIFIER | c.-3569G>A| |
S34 |
7 | BAA02g44310 | A02 | 36543235 | C | T | upstream_gene_variant | MODIFIER | c.-2879C>T| |
S117 |
8 | BAA02g44310 | A02 | 36546450 | G | A | missense_variant | MODERATE | c.337G>A|p.Ala113Thr |
S111 |
9 | BAA02g44310 | A02 | 36546783 | C | T | synonymous_variant | LOW | c.582C>T|p.Arg194Arg |
S212 |
10 | BAA02g44310 | A02 | 36547445 | G | A | missense_variant | MODERATE | c.1124G>A|p.Arg375Lys |
S246 |
11 | BAA02g44310 | A02 | 36547562 | C | T | missense_variant | MODERATE | c.1241C>T|p.Ser414Leu |
S140 |
12 | BAA02g44310 | A02 | 36547624 | G | A | missense_variant | MODERATE | c.1303G>A|p.Val435Ile |
S134 |
13 | BAA02g44310 | A02 | 36547900 | G | A | missense_variant | MODERATE | c.1579G>A|p.Val527Ile |
S238 |
14 | BAA02g44310 | A02 | 36548225 | G | A | stop_gained | HIGH | c.1904G>A|p.Trp635* |
S200 |
15 | BAA02g44310 | A02 | 36548324 | C | T | missense_variant | MODERATE | c.2003C>T|p.Thr668Ile |
S172 S217 |