Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g08910 | A05 | 4444219 | C | T | upstream_gene_variant | MODIFIER | c.-3331C>T| |
S5 |
2 | BAA05g08910 | A05 | 4444254 | G | A | upstream_gene_variant | MODIFIER | c.-3296G>A| |
S94 |
3 | BAA05g08910 | A05 | 4444350 | G | A | upstream_gene_variant | MODIFIER | c.-3200G>A| |
|
4 | BAA05g08910 | A05 | 4444473 | A | T | upstream_gene_variant | MODIFIER | c.-3077A>T| |
S7 |
5 | BAA05g08910 | A05 | 4444801 | G | A | upstream_gene_variant | MODIFIER | c.-2749G>A| |
S233 |
6 | BAA05g08910 | A05 | 4445079 | C | T | upstream_gene_variant | MODIFIER | c.-2471C>T| |
S277 |
7 | BAA05g08910 | A05 | 4445081 | C | T | upstream_gene_variant | MODIFIER | c.-2469C>T| |
S18 |
8 | BAA05g08910 | A05 | 4447151 | T | C | upstream_gene_variant | MODIFIER | c.-399T>C| |
S67 |
9 | BAA05g08910 | A05 | 4448292 | G | A | missense_variant | MODERATE | c.413G>A|p.Gly138Glu |
S80 |
10 | BAA05g08910 | A05 | 4448517 | C | T | synonymous_variant | LOW | c.547C>T|p.Leu183Leu |
S51 |
11 | BAA05g08910 | A05 | 4453866 | C | T | downstream_gene_variant | MODIFIER | c.*4952C>T| |
S278 |