Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g27970 | A02 | 15754822 | C | T | upstream_gene_variant | MODIFIER | c.-1475C>T| |
S299 |
2 | BAA02g27970 | A02 | 15755024 | C | T | upstream_gene_variant | MODIFIER | c.-1273C>T| |
S167 |
3 | BAA02g27970 | A02 | 15755669 | G | A | upstream_gene_variant | MODIFIER | c.-628G>A| |
S251 |
4 | BAA02g27970 | A02 | 15755726 | G | A | upstream_gene_variant | MODIFIER | c.-571G>A| |
S260 |
5 | BAA02g27970 | A02 | 15755745 | C | T | upstream_gene_variant | MODIFIER | c.-552C>T| |
S110 S162 |
6 | BAA02g27970 | A02 | 15755764 | C | T | upstream_gene_variant | MODIFIER | c.-533C>T| |
S226 |
7 | BAA02g27970 | A02 | 15755998 | C | T | upstream_gene_variant | MODIFIER | c.-299C>T| |
S52 |
8 | BAA02g27970 | A02 | 15756568 | G | A | synonymous_variant | LOW | c.192G>A|p.Ser64Ser |
S125 |
9 | BAA02g27970 | A02 | 15757607 | C | T | synonymous_variant | LOW | c.804C>T|p.Arg268Arg |
S63 |
10 | BAA02g27970 | A02 | 15757624 | G | A | missense_variant | MODERATE | c.821G>A|p.Gly274Glu |
S302 |
11 | BAA02g27970 | A02 | 15761983 | C | T | downstream_gene_variant | MODIFIER | c.*4115C>T| |
S164 |
12 | BAA02g27970 | A02 | 15762022 | C | T | downstream_gene_variant | MODIFIER | c.*4154C>T| |
S180 |