Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g17740 | A01 | 8609168 | C | T | upstream_gene_variant | MODIFIER | c.-3685C>T| |
S149 |
2 | BAA01g17740 | A01 | 8609206 | G | A | upstream_gene_variant | MODIFIER | c.-3647G>A| |
S204 |
3 | BAA01g17740 | A01 | 8610150 | G | A | upstream_gene_variant | MODIFIER | c.-2703G>A| |
S174 |
4 | BAA01g17740 | A01 | 8610234 | G | A | upstream_gene_variant | MODIFIER | c.-2619G>A| |
S153 |
5 | BAA01g17740 | A01 | 8611117 | C | T | upstream_gene_variant | MODIFIER | c.-1736C>T| |
S182 |
6 | BAA01g17740 | A01 | 8612382 | G | A | upstream_gene_variant | MODIFIER | c.-471G>A| |
S280 |
7 | BAA01g17740 | A01 | 8612391 | G | A | upstream_gene_variant | MODIFIER | c.-462G>A| |
S278 |
8 | BAA01g17740 | A01 | 8613443 | C | T | intron_variant | MODIFIER | c.467+43C>T| |
S118 |
9 | BAA01g17740 | A01 | 8613512 | G | A | intron_variant | MODIFIER | c.467+112G>A| |
S124 |
10 | BAA01g17740 | A01 | 8614411 | G | A | downstream_gene_variant | MODIFIER | c.*102G>A| |
S181 |
11 | BAA01g17740 | A01 | 8616696 | G | A | downstream_gene_variant | MODIFIER | c.*2387G>A| |
S217 |
12 | BAA01g17740 | A01 | 8616901 | G | A | downstream_gene_variant | MODIFIER | c.*2592G>A| |
S162 |
13 | BAA01g17740 | A01 | 8617237 | G | A | downstream_gene_variant | MODIFIER | c.*2928G>A| |
S186 |
14 | BAA01g17740 | A01 | 8617270 | C | T | downstream_gene_variant | MODIFIER | c.*2961C>T| |
S303 |
15 | BAA01g17740 | A01 | 8617447 | C | T | downstream_gene_variant | MODIFIER | c.*3138C>T| |
S53 |
16 | BAA01g17740 | A01 | 8618033 | G | A | downstream_gene_variant | MODIFIER | c.*3724G>A| |
S291 |
17 | BAA01g17740 | A01 | 8618333 | G | A | downstream_gene_variant | MODIFIER | c.*4024G>A| |
S172 S217 |
18 | BAA01g17740 | A01 | 8618456 | G | A | downstream_gene_variant | MODIFIER | c.*4147G>A| |
S195 |