Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g18850 | A02 | 9703601 | C | T | downstream_gene_variant | MODIFIER | c.*1532G>A| |
S167 |
2 | BAA02g18850 | A02 | 9703667 | C | T | downstream_gene_variant | MODIFIER | c.*1466G>A| |
S8 |
3 | BAA02g18850 | A02 | 9705177 | C | T | missense_variant | MODERATE | c.3004G>A|p.Asp1002Asn |
S121 |
4 | BAA02g18850 | A02 | 9705609 | C | T | missense_variant | MODERATE | c.2665G>A|p.Val889Ile |
S209 |
5 | BAA02g18850 | A02 | 9705703 | C | T | synonymous_variant | LOW | c.2637G>A|p.Lys879Lys |
S138 |
6 | BAA02g18850 | A02 | 9705775 | C | T | synonymous_variant | LOW | c.2565G>A|p.Leu855Leu |
S163 |
7 | BAA02g18850 | A02 | 9705799 | C | T | synonymous_variant | LOW | c.2541G>A|p.Val847Val |
S135 |
8 | BAA02g18850 | A02 | 9706113 | C | T | missense_variant | MODERATE | c.2227G>A|p.Ala743Thr |
S186 |
9 | BAA02g18850 | A02 | 9708290 | G | A | stop_gained | HIGH | c.718C>T|p.Gln240* |
S281 S282 |
10 | BAA02g18850 | A02 | 9709353 | C | T | synonymous_variant | LOW | c.45G>A|p.Gln15Gln |
S34 |
11 | BAA02g18850 | A02 | 9709577 | C | T | upstream_gene_variant | MODIFIER | c.-84G>A| |
S58 |
12 | BAA02g18850 | A02 | 9710522 | G | A | upstream_gene_variant | MODIFIER | c.-1029C>T| |
S291 |
13 | BAA02g18850 | A02 | 9710562 | C | T | upstream_gene_variant | MODIFIER | c.-1069G>A| |
S94 |
14 | BAA02g18850 | A02 | 9710714 | A | G | upstream_gene_variant | MODIFIER | c.-1221T>C| |
S282 |
15 | BAA02g18850 | A02 | 9711024 | G | A | upstream_gene_variant | MODIFIER | c.-1531C>T| |
S257 |
16 | BAA02g18850 | A02 | 9711064 | A | T | upstream_gene_variant | MODIFIER | c.-1571T>A| |
S218 S232 S243 S244 S42 |