Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g67000 | A03 | 41498567 | C | T | downstream_gene_variant | MODIFIER | c.*1325G>A| |
S45 |
2 | BAA03g67000 | A03 | 41499571 | C | T | downstream_gene_variant | MODIFIER | c.*321G>A| |
S57 |
3 | BAA03g67000 | A03 | 41499648 | G | A | downstream_gene_variant | MODIFIER | c.*244C>T| |
S124 |
4 | BAA03g67000 | A03 | 41499966 | C | T | missense_variant | MODERATE | c.85G>A|p.Ala29Thr |
S45 |
5 | BAA03g67000 | A03 | 41500057 | G | A | intron_variant | MODIFIER | c.70-76C>T| |
S112 |
6 | BAA03g67000 | A03 | 41500514 | G | A | intron_variant | MODIFIER | c.70-533C>T| |
S111 |
7 | BAA03g67000 | A03 | 41500898 | G | A | intron_variant | MODIFIER | c.70-917C>T| |
S202 |
8 | BAA03g67000 | A03 | 41502637 | G | A | upstream_gene_variant | MODIFIER | c.-139C>T| |
S11 |
9 | BAA03g67000 | A03 | 41502902 | G | A | upstream_gene_variant | MODIFIER | c.-404C>T| |
S259 |
10 | BAA03g67000 | A03 | 41502984 | C | T | upstream_gene_variant | MODIFIER | c.-486G>A| |
S103 |
11 | BAA03g67000 | A03 | 41504964 | G | A | upstream_gene_variant | MODIFIER | c.-2466C>T| |
S149 |
12 | BAA03g67000 | A03 | 41504995 | C | T | upstream_gene_variant | MODIFIER | c.-2497G>A| |
S192 |
13 | BAA03g67000 | A03 | 41505133 | C | T | upstream_gene_variant | MODIFIER | c.-2635G>A| |
S59 |
14 | BAA03g67000 | A03 | 41505481 | G | A | upstream_gene_variant | MODIFIER | c.-2983C>T| |
S182 |
15 | BAA03g67000 | A03 | 41505549 | G | A | upstream_gene_variant | MODIFIER | c.-3051C>T| |
S152 |
16 | BAA03g67000 | A03 | 41505655 | C | T | upstream_gene_variant | MODIFIER | c.-3157G>A| |
S134 |
17 | BAA03g67000 | A03 | 41505663 | C | T | upstream_gene_variant | MODIFIER | c.-3165G>A| |
S119 |
18 | BAA03g67000 | A03 | 41506263 | C | T | upstream_gene_variant | MODIFIER | c.-3765G>A| |
S263 |