Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g41990 | A02 | 35045824 | C | T | synonymous_variant | LOW | c.513C>T|p.Tyr171Tyr |
S252 |
2 | BAA02g41990 | A02 | 35048939 | C | T | synonymous_variant | LOW | c.2196C>T|p.Ser732Ser |
S61 |
3 | BAA02g41990 | A02 | 35048998 | A | G | missense_variant | MODERATE | c.2255A>G|p.Gln752Arg |
S226 |
4 | BAA02g41990 | A02 | 35050324 | C | T | missense_variant | MODERATE | c.3478C>T|p.Leu1160Phe |
S239 |
5 | BAA02g41990 | A02 | 35051198 | G | A | missense_variant | MODERATE | c.4195G>A|p.Glu1399Lys |
S281 |
6 | BAA02g41990 | A02 | 35051201 | G | A | missense_variant | MODERATE | c.4198G>A|p.Gly1400Arg |
S35 |
7 | BAA02g41990 | A02 | 35052144 | G | A | downstream_gene_variant | MODIFIER | c.*860G>A| |
S11 |
8 | BAA02g41990 | A02 | 35052309 | C | T | downstream_gene_variant | MODIFIER | c.*1025C>T| |
S181 |
9 | BAA02g41990 | A02 | 35054385 | C | T | downstream_gene_variant | MODIFIER | c.*3101C>T| |
S158 |