Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g08380 | A05 | 4164467 | C | T | upstream_gene_variant | MODIFIER | c.-4671C>T| |
S119 |
2 | BAA05g08380 | A05 | 4164539 | C | T | upstream_gene_variant | MODIFIER | c.-4599C>T| |
S201 |
3 | BAA05g08380 | A05 | 4165484 | G | A | upstream_gene_variant | MODIFIER | c.-3654G>A| |
S166 |
4 | BAA05g08380 | A05 | 4165753 | G | A | upstream_gene_variant | MODIFIER | c.-3385G>A| |
S138 |
5 | BAA05g08380 | A05 | 4165855 | G | A | upstream_gene_variant | MODIFIER | c.-3283G>A| |
S48 |
6 | BAA05g08380 | A05 | 4166045 | G | A | upstream_gene_variant | MODIFIER | c.-3093G>A| |
S301 S304 |
7 | BAA05g08380 | A05 | 4166290 | G | A | upstream_gene_variant | MODIFIER | c.-2848G>A| |
S247 |
8 | BAA05g08380 | A05 | 4166325 | C | T | upstream_gene_variant | MODIFIER | c.-2813C>T| |
S178 S216 |
9 | BAA05g08380 | A05 | 4166942 | T | C | upstream_gene_variant | MODIFIER | c.-2196T>C| |
S159 |
10 | BAA05g08380 | A05 | 4171660 | G | A | missense_variant | MODERATE | c.925G>A|p.Gly309Arg |
S46 |
11 | BAA05g08380 | A05 | 4171860 | G | A | synonymous_variant | LOW | c.1047G>A|p.Leu349Leu |
S11 |