Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g43170 | A02 | 35846354 | G | A | missense_variant | MODERATE | c.1073C>T|p.Ser358Phe |
S169 |
2 | BAA02g43170 | A02 | 35846623 | G | A | synonymous_variant | LOW | c.804C>T|p.Asp268Asp |
S35 |
3 | BAA02g43170 | A02 | 35846903 | G | A | missense_variant | MODERATE | c.524C>T|p.Pro175Leu |
S111 |
4 | BAA02g43170 | A02 | 35847144 | G | A | synonymous_variant | LOW | c.283C>T|p.Leu95Leu |
S148 S30 |
5 | BAA02g43170 | A02 | 35847165 | C | T | missense_variant | MODERATE | c.262G>A|p.Gly88Arg |
S221 |
6 | BAA02g43170 | A02 | 35847422 | G | A | missense_variant | MODERATE | c.5C>T|p.Thr2Ile |
S281 |
7 | BAA02g43170 | A02 | 35847642 | G | A | upstream_gene_variant | MODIFIER | c.-216C>T| |
S79 S91 |
8 | BAA02g43170 | A02 | 35847643 | G | A | upstream_gene_variant | MODIFIER | c.-217C>T| |
S8 |
9 | BAA02g43170 | A02 | 35848502 | C | T | upstream_gene_variant | MODIFIER | c.-1076G>A| |
S39 |
10 | BAA02g43170 | A02 | 35848864 | G | A | upstream_gene_variant | MODIFIER | c.-1438C>T| |
S69 |
11 | BAA02g43170 | A02 | 35848996 | C | T | upstream_gene_variant | MODIFIER | c.-1570G>A| |
S212 |
12 | BAA02g43170 | A02 | 35849371 | C | T | upstream_gene_variant | MODIFIER | c.-1945G>A| |
S170 |