Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g40600 | A02 | 34176367 | G | A | missense_variant | MODERATE | c.658C>T|p.Pro220Ser |
S306 S308 |
2 | BAA02g40600 | A02 | 34178337 | G | A | missense_variant | MODERATE | c.110C>T|p.Thr37Ile |
S172 S202 |
3 | BAA02g40600 | A02 | 34178774 | C | T | upstream_gene_variant | MODIFIER | c.-328G>A| |
S3 |
4 | BAA02g40600 | A02 | 34178873 | C | T | upstream_gene_variant | MODIFIER | c.-427G>A| |
S266 |
5 | BAA02g40600 | A02 | 34179632 | G | A | upstream_gene_variant | MODIFIER | c.-1186C>T| |
S251 |
6 | BAA02g40600 | A02 | 34180671 | C | T | upstream_gene_variant | MODIFIER | c.-2225G>A| |
S308 |
7 | BAA02g40600 | A02 | 34180941 | G | A | upstream_gene_variant | MODIFIER | c.-2495C>T| |
S268 |
8 | BAA02g40600 | A02 | 34180988 | C | T | upstream_gene_variant | MODIFIER | c.-2542G>A| |
S266 |
9 | BAA02g40600 | A02 | 34183019 | G | A | upstream_gene_variant | MODIFIER | c.-4573C>T| |
S200 |