Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g11810 | A05 | 5985328 | G | A | upstream_gene_variant | MODIFIER | c.-4131G>A| |
S149 |
2 | BAA05g11810 | A05 | 5986100 | C | T | upstream_gene_variant | MODIFIER | c.-3359C>T| |
S292 |
3 | BAA05g11810 | A05 | 5988432 | G | A | upstream_gene_variant | MODIFIER | c.-1027G>A| |
S210 |
4 | BAA05g11810 | A05 | 5988452 | C | T | upstream_gene_variant | MODIFIER | c.-1007C>T| |
S105 S106 |
5 | BAA05g11810 | A05 | 5988611 | C | T | upstream_gene_variant | MODIFIER | c.-848C>T| |
S185 |
6 | BAA05g11810 | A05 | 5988677 | G | A | upstream_gene_variant | MODIFIER | c.-782G>A| |
S293 |
7 | BAA05g11810 | A05 | 5988890 | C | T | upstream_gene_variant | MODIFIER | c.-569C>T| |
S72 S78 |
8 | BAA05g11810 | A05 | 5989407 | C | T | upstream_gene_variant | MODIFIER | c.-52C>T| |
S81 S85 |
9 | BAA05g11810 | A05 | 5991094 | C | T | missense_variant | MODERATE | c.409C>T|p.Leu137Phe |
S89 |
10 | BAA05g11810 | A05 | 5991726 | G | A | missense_variant | MODERATE | c.829G>A|p.Glu277Lys |
S32 |
11 | BAA05g11810 | A05 | 5992302 | C | T | missense_variant&splice_region_variant | MODERATE | c.1165C>T|p.Pro389Ser |
S36 |
12 | BAA05g11810 | A05 | 5992794 | G | A | downstream_gene_variant | MODIFIER | c.*134G>A| |
S144 |