Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g13980 | A02 | 6563200 | C | T | upstream_gene_variant | MODIFIER | c.-4458C>T| |
S221 |
2 | BAA02g13980 | A02 | 6564119 | C | T | upstream_gene_variant | MODIFIER | c.-3539C>T| |
S65 |
3 | BAA02g13980 | A02 | 6564439 | C | T | upstream_gene_variant | MODIFIER | c.-3219C>T| |
S100 |
4 | BAA02g13980 | A02 | 6564644 | G | A | upstream_gene_variant | MODIFIER | c.-3014G>A| |
S136 |
5 | BAA02g13980 | A02 | 6564981 | C | T | upstream_gene_variant | MODIFIER | c.-2677C>T| |
S183 S198 |
6 | BAA02g13980 | A02 | 6566278 | C | T | upstream_gene_variant | MODIFIER | c.-1380C>T| |
S181 |
7 | BAA02g13980 | A02 | 6566350 | C | T | upstream_gene_variant | MODIFIER | c.-1308C>T| |
S114 |
8 | BAA02g13980 | A02 | 6567136 | G | A | upstream_gene_variant | MODIFIER | c.-522G>A| |
S294 |
9 | BAA02g13980 | A02 | 6567762 | G | A | synonymous_variant | LOW | c.105G>A|p.Glu35Glu |
S148 S30 S31 |
10 | BAA02g13980 | A02 | 6568156 | G | A | missense_variant | MODERATE | c.335G>A|p.Cys112Tyr |
S23 |
11 | BAA02g13980 | A02 | 6568230 | G | A | missense_variant | MODERATE | c.409G>A|p.Val137Ile |
S170 |
12 | BAA02g13980 | A02 | 6568903 | G | A | missense_variant | MODERATE | c.1082G>A|p.Arg361Lys |
S11 |
13 | BAA02g13980 | A02 | 6569229 | G | A | missense_variant | MODERATE | c.1327G>A|p.Asp443Asn |
S279 |
14 | BAA02g13980 | A02 | 6569929 | G | A | missense_variant | MODERATE | c.2027G>A|p.Gly676Glu |
S198 |
15 | BAA02g13980 | A02 | 6569979 | C | T | missense_variant | MODERATE | c.2077C>T|p.Pro693Ser |
S308 |
16 | BAA02g13980 | A02 | 6570656 | C | T | synonymous_variant | LOW | c.2754C>T|p.Ser918Ser |
S128 |
17 | BAA02g13980 | A02 | 6572753 | G | A | downstream_gene_variant | MODIFIER | c.*1983G>A| |
S13 S168 S279 S64 |
18 | BAA02g13980 | A02 | 6572798 | G | A | downstream_gene_variant | MODIFIER | c.*2028G>A| |
S23 |