Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g23380 | A01 | 12031785 | C | T | synonymous_variant | LOW | c.1038C>T|p.Phe346Phe |
S185 |
2 | BAA01g23380 | A01 | 12031851 | C | T | synonymous_variant | LOW | c.1104C>T|p.Pro368Pro |
S249 |
3 | BAA01g23380 | A01 | 12032813 | G | T | missense_variant | MODERATE | c.1394G>T|p.Cys465Phe |
S174 S216 S241 S39 |
4 | BAA01g23380 | A01 | 12033164 | A | G | missense_variant | MODERATE | c.1618A>G|p.Thr540Ala |
S38 |
5 | BAA01g23380 | A01 | 12033188 | G | A | missense_variant | MODERATE | c.1642G>A|p.Glu548Lys |
S172 S217 |
6 | BAA01g23380 | A01 | 12034282 | C | T | downstream_gene_variant | MODIFIER | c.*407C>T| |
S264 |
7 | BAA01g23380 | A01 | 12034877 | C | T | downstream_gene_variant | MODIFIER | c.*1002C>T| |
S16 |
8 | BAA01g23380 | A01 | 12035992 | G | A | downstream_gene_variant | MODIFIER | c.*2117G>A| |
S238 |