Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g17230 | A01 | 8351600 | C | T | missense_variant | MODERATE | c.1396G>A|p.Ala466Thr |
S242 |
2 | BAA01g17230 | A01 | 8351630 | C | T | missense_variant | MODERATE | c.1366G>A|p.Gly456Arg |
S249 |
3 | BAA01g17230 | A01 | 8352187 | G | A | missense_variant | MODERATE | c.809C>T|p.Thr270Ile |
S74 |
4 | BAA01g17230 | A01 | 8352438 | C | T | synonymous_variant | LOW | c.558G>A|p.Gln186Gln |
S243 |
5 | BAA01g17230 | A01 | 8352691 | G | A | missense_variant | MODERATE | c.305C>T|p.Thr102Ile |
S23 |
6 | BAA01g17230 | A01 | 8352795 | C | T | synonymous_variant | LOW | c.201G>A|p.Arg67Arg |
S169 |
7 | BAA01g17230 | A01 | 8356448 | C | T | upstream_gene_variant | MODIFIER | c.-3453G>A| |
S87 |
8 | BAA01g17230 | A01 | 8356795 | G | A | upstream_gene_variant | MODIFIER | c.-3800C>T| |
S94 |
9 | BAA01g17230 | A01 | 8357031 | C | T | upstream_gene_variant | MODIFIER | c.-4036G>A| |
S132 S137 |
10 | BAA01g17230 | A01 | 8357646 | G | A | upstream_gene_variant | MODIFIER | c.-4651C>T| |
S86 |