Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g39990 | A01 | 26559272 | C | T | downstream_gene_variant | MODIFIER | c.*2087G>A| |
S205 |
2 | BAA01g39990 | A01 | 26559744 | G | A | downstream_gene_variant | MODIFIER | c.*1615C>T| |
S105 S106 |
3 | BAA01g39990 | A01 | 26560743 | G | A | downstream_gene_variant | MODIFIER | c.*616C>T| |
S163 |
4 | BAA01g39990 | A01 | 26561975 | G | A | intron_variant | MODIFIER | c.1643-32C>T| |
S8 |
5 | BAA01g39990 | A01 | 26562530 | G | A | intron_variant | MODIFIER | c.1377-143C>T| |
S195 |
6 | BAA01g39990 | A01 | 26563167 | C | T | synonymous_variant | LOW | c.1026G>A|p.Lys342Lys |
S230 |
7 | BAA01g39990 | A01 | 26563945 | G | T | intron_variant | MODIFIER | c.651-10C>A| |
S149 |
8 | BAA01g39990 | A01 | 26563946 | A | T | intron_variant | MODIFIER | c.651-11T>A| |
S149 |
9 | BAA01g39990 | A01 | 26564536 | C | T | missense_variant&splice_region_variant | MODERATE | c.448G>A|p.Glu150Lys |
S198 |
10 | BAA01g39990 | A01 | 26564759 | C | T | intron_variant | MODIFIER | c.322-97G>A| |
S203 |
11 | BAA01g39990 | A01 | 26564888 | C | T | intron_variant | MODIFIER | c.321+218G>A| |
S139 |
12 | BAA01g39990 | A01 | 26564958 | C | T | intron_variant | MODIFIER | c.321+148G>A| |
S159 S243 |
13 | BAA01g39990 | A01 | 26565274 | C | T | synonymous_variant | LOW | c.153G>A|p.Lys51Lys |
S39 |
14 | BAA01g39990 | A01 | 26565371 | G | A | missense_variant | MODERATE | c.56C>T|p.Ala19Val |
S245 |
15 | BAA01g39990 | A01 | 26568966 | C | T | upstream_gene_variant | MODIFIER | c.-3540G>A| |
S148 S30 S31 |
16 | BAA01g39990 | A01 | 26569060 | C | T | upstream_gene_variant | MODIFIER | c.-3634G>A| |
S264 |
17 | BAA01g39990 | A01 | 26570027 | C | T | upstream_gene_variant | MODIFIER | c.-4601G>A| |
S206 S26 |