Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g02390 | A08 | 1716397 | G | A | missense_variant | MODERATE | c.464C>T|p.Ala155Val |
S185 |
2 | BAA08g02390 | A08 | 1717278 | C | T | intron_variant | MODIFIER | c.274-223G>A| |
S132 S137 S89 |
3 | BAA08g02390 | A08 | 1717354 | G | A | intron_variant | MODIFIER | c.274-299C>T| |
S160 S199 |
4 | BAA08g02390 | A08 | 1718363 | C | T | intron_variant | MODIFIER | c.273+686G>A| |
S276 |
5 | BAA08g02390 | A08 | 1719101 | G | A | missense_variant | MODERATE | c.221C>T|p.Ser74Phe |
S16 |
6 | BAA08g02390 | A08 | 1723083 | C | T | upstream_gene_variant | MODIFIER | c.-3680G>A| |
S80 |
7 | BAA08g02390 | A08 | 1723198 | C | T | upstream_gene_variant | MODIFIER | c.-3795G>A| |
S71 |
8 | BAA08g02390 | A08 | 1724246 | C | T | upstream_gene_variant | MODIFIER | c.-4843G>A| |
S70 |