Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g16090 | A02 | 7823870 | C | T | missense_variant | MODERATE | c.233C>T|p.Ser78Phe |
S270 |
2 | BAA02g16090 | A02 | 7824050 | C | T | missense_variant | MODERATE | c.413C>T|p.Pro138Leu |
S179 |
3 | BAA02g16090 | A02 | 7824194 | G | A | missense_variant | MODERATE | c.557G>A|p.Arg186Lys |
S7 |
4 | BAA02g16090 | A02 | 7824263 | G | A | missense_variant | MODERATE | c.626G>A|p.Arg209Lys |
S238 |
5 | BAA02g16090 | A02 | 7824656 | G | A | missense_variant | MODERATE | c.1019G>A|p.Ser340Asn |
S56 |
6 | BAA02g16090 | A02 | 7825614 | G | A | synonymous_variant | LOW | c.1977G>A|p.Lys659Lys |
S132 S137 S215 |
7 | BAA02g16090 | A02 | 7826108 | G | A | missense_variant | MODERATE | c.2300G>A|p.Gly767Glu |
S150 |
8 | BAA02g16090 | A02 | 7826305 | G | A | missense_variant | MODERATE | c.2497G>A|p.Glu833Lys |
S231 |
9 | BAA02g16090 | A02 | 7826440 | T | A | missense_variant | MODERATE | c.2632T>A|p.Ser878Thr |
S35 |
10 | BAA02g16090 | A02 | 7828247 | G | A | downstream_gene_variant | MODIFIER | c.*1616G>A| |
S132 S137 S215 S89 |