Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g19770 | A08 | 15475377 | G | A | missense_variant | MODERATE | c.157G>A|p.Val53Ile |
S239 |
2 | BAA08g19770 | A08 | 15475602 | G | A | missense_variant | MODERATE | c.382G>A|p.Gly128Arg |
S292 |
3 | BAA08g19770 | A08 | 15476576 | C | T | missense_variant | MODERATE | c.803C>T|p.Pro268Leu |
S58 |
4 | BAA08g19770 | A08 | 15477141 | C | T | stop_gained | HIGH | c.1192C>T|p.Gln398* |
S178 |
5 | BAA08g19770 | A08 | 15477418 | G | A | missense_variant | MODERATE | c.1469G>A|p.Gly490Glu |
S124 |
6 | BAA08g19770 | A08 | 15477691 | G | A | missense_variant | MODERATE | c.1742G>A|p.Gly581Glu |
S262 |
7 | BAA08g19770 | A08 | 15480180 | C | T | downstream_gene_variant | MODIFIER | c.*2266C>T| |
S244 |
8 | BAA08g19770 | A08 | 15482508 | C | T | downstream_gene_variant | MODIFIER | c.*4594C>T| |
S181 |