Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g05840 | A02 | 2486004 | C | T | upstream_gene_variant | MODIFIER | c.-4873C>T| |
S68 |
2 | BAA02g05840 | A02 | 2486282 | C | T | upstream_gene_variant | MODIFIER | c.-4595C>T| |
S40 S49 |
3 | BAA02g05840 | A02 | 2487099 | G | A | upstream_gene_variant | MODIFIER | c.-3778G>A| |
S125 |
4 | BAA02g05840 | A02 | 2487907 | C | T | upstream_gene_variant | MODIFIER | c.-2970C>T| |
S6 |
5 | BAA02g05840 | A02 | 2488399 | G | A | upstream_gene_variant | MODIFIER | c.-2478G>A| |
S169 S173 |
6 | BAA02g05840 | A02 | 2488865 | C | T | upstream_gene_variant | MODIFIER | c.-2012C>T| |
S277 |
7 | BAA02g05840 | A02 | 2490898 | G | A | missense_variant | MODERATE | c.22G>A|p.Glu8Lys |
S269 |
8 | BAA02g05840 | A02 | 2491278 | G | A | splice_region_variant&intron_variant | LOW | c.234+7G>A| |
S10 |
9 | BAA02g05840 | A02 | 2492323 | C | T | missense_variant | MODERATE | c.778C>T|p.Arg260Trp |
S19 |
10 | BAA02g05840 | A02 | 2492491 | G | A | missense_variant | MODERATE | c.946G>A|p.Glu316Lys |
S53 |
11 | BAA02g05840 | A02 | 2494992 | G | A | downstream_gene_variant | MODIFIER | c.*1972G>A| |
S68 |