Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g35070 | A02 | 30174230 | C | T | upstream_gene_variant | MODIFIER | c.-4155C>T| |
S181 |
2 | BAA02g35070 | A02 | 30174313 | G | A | upstream_gene_variant | MODIFIER | c.-4072G>A| |
S80 |
3 | BAA02g35070 | A02 | 30174702 | C | T | upstream_gene_variant | MODIFIER | c.-3683C>T| |
S6 |
4 | BAA02g35070 | A02 | 30175806 | G | A | upstream_gene_variant | MODIFIER | c.-2579G>A| |
S43 |
5 | BAA02g35070 | A02 | 30177315 | G | A | upstream_gene_variant | MODIFIER | c.-1070G>A| |
S288 |
6 | BAA02g35070 | A02 | 30178267 | G | A | upstream_gene_variant | MODIFIER | c.-118G>A| |
S279 |
7 | BAA02g35070 | A02 | 30178463 | G | A | missense_variant | MODERATE | c.79G>A|p.Asp27Asn |
S94 |
8 | BAA02g35070 | A02 | 30179379 | C | T | synonymous_variant | LOW | c.747C>T|p.Asp249Asp |
S189 |
9 | BAA02g35070 | A02 | 30179497 | G | A | missense_variant | MODERATE | c.865G>A|p.Asp289Asn |
S168 |
10 | BAA02g35070 | A02 | 30179916 | G | A | downstream_gene_variant | MODIFIER | c.*381G>A| |
S13 |
11 | BAA02g35070 | A02 | 30180100 | G | A | downstream_gene_variant | MODIFIER | c.*565G>A| |
S287 |
12 | BAA02g35070 | A02 | 30180315 | C | T | downstream_gene_variant | MODIFIER | c.*780C>T| |
S257 |
13 | BAA02g35070 | A02 | 30181838 | G | A | downstream_gene_variant | MODIFIER | c.*2303G>A| |
S50 S51 |
14 | BAA02g35070 | A02 | 30182981 | C | T | downstream_gene_variant | MODIFIER | c.*3446C>T| |
S98 |
15 | BAA02g35070 | A02 | 30183075 | C | T | downstream_gene_variant | MODIFIER | c.*3540C>T| |
S88 |