Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g22870 | A02 | 12403472 | C | T | upstream_gene_variant | MODIFIER | c.-4754C>T| |
S56 |
2 | BAA02g22870 | A02 | 12403495 | C | T | upstream_gene_variant | MODIFIER | c.-4731C>T| |
S53 |
3 | BAA02g22870 | A02 | 12403721 | C | T | upstream_gene_variant | MODIFIER | c.-4505C>T| |
S201 |
4 | BAA02g22870 | A02 | 12405277 | G | A | upstream_gene_variant | MODIFIER | c.-2949G>A| |
S139 |
5 | BAA02g22870 | A02 | 12406257 | G | A | upstream_gene_variant | MODIFIER | c.-1969G>A| |
S58 |
6 | BAA02g22870 | A02 | 12406959 | G | A | upstream_gene_variant | MODIFIER | c.-1267G>A| |
S162 |
7 | BAA02g22870 | A02 | 12407220 | C | T | upstream_gene_variant | MODIFIER | c.-1006C>T| |
S216 |
8 | BAA02g22870 | A02 | 12408021 | G | A | upstream_gene_variant | MODIFIER | c.-205G>A| |
S48 |
9 | BAA02g22870 | A02 | 12408290 | C | T | missense_variant | MODERATE | c.65C>T|p.Ser22Phe |
S267 |
10 | BAA02g22870 | A02 | 12408405 | G | A | synonymous_variant | LOW | c.180G>A|p.Ala60Ala |
S47 |
11 | BAA02g22870 | A02 | 12408452 | G | A | missense_variant | MODERATE | c.227G>A|p.Gly76Asp |
S188 |
12 | BAA02g22870 | A02 | 12411107 | G | A | missense_variant&splice_region_variant | MODERATE | c.2006G>A|p.Gly669Glu |
S228 |
13 | BAA02g22870 | A02 | 12412499 | G | A | downstream_gene_variant | MODIFIER | c.*638G>A| |
S7 |
14 | BAA02g22870 | A02 | 12412734 | C | T | downstream_gene_variant | MODIFIER | c.*873C>T| |
S208 S219 |