Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g47630 | A02 | 38368090 | G | A | upstream_gene_variant | MODIFIER | c.-3017G>A| |
S243 S299 |
2 | BAA02g47630 | A02 | 38370563 | G | A | upstream_gene_variant | MODIFIER | c.-544G>A| |
S152 |
3 | BAA02g47630 | A02 | 38371146 | C | T | missense_variant | MODERATE | c.40C>T|p.Pro14Ser |
S192 |
4 | BAA02g47630 | A02 | 38371943 | G | A | missense_variant | MODERATE | c.619G>A|p.Gly207Arg |
S229 |
5 | BAA02g47630 | A02 | 38372177 | G | A | missense_variant | MODERATE | c.853G>A|p.Glu285Lys |
S81 S85 |
6 | BAA02g47630 | A02 | 38372285 | C | T | missense_variant | MODERATE | c.961C>T|p.Leu321Phe |
S255 |
7 | BAA02g47630 | A02 | 38372437 | G | A | synonymous_variant | LOW | c.1113G>A|p.Lys371Lys |
S124 |
8 | BAA02g47630 | A02 | 38372913 | G | A | missense_variant | MODERATE | c.1589G>A|p.Gly530Glu |
S238 |
9 | BAA02g47630 | A02 | 38372970 | C | T | missense_variant | MODERATE | c.1646C>T|p.Ser549Phe |
S121 |
10 | BAA02g47630 | A02 | 38378373 | G | A | downstream_gene_variant | MODIFIER | c.*4922G>A| |
S10 |