Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g12150 | A05 | 6172058 | C | T | downstream_gene_variant | MODIFIER | c.*3038G>A| |
S270 |
2 | BAA05g12150 | A05 | 6172219 | G | A | downstream_gene_variant | MODIFIER | c.*2877C>T| |
S274 |
3 | BAA05g12150 | A05 | 6173783 | G | A | downstream_gene_variant | MODIFIER | c.*1313C>T| |
S79 S91 |
4 | BAA05g12150 | A05 | 6173786 | G | A | downstream_gene_variant | MODIFIER | c.*1310C>T| |
S148 S210 |
5 | BAA05g12150 | A05 | 6173825 | C | T | downstream_gene_variant | MODIFIER | c.*1271G>A| |
S13 S219 S239 S278 S33 S64 S72 |
6 | BAA05g12150 | A05 | 6175293 | C | T | missense_variant | MODERATE | c.121G>A|p.Gly41Ser |
S163 |
7 | BAA05g12150 | A05 | 6175339 | C | T | missense_variant | MODERATE | c.75G>A|p.Met25Ile |
S205 |
8 | BAA05g12150 | A05 | 6175717 | G | A | upstream_gene_variant | MODIFIER | c.-96C>T| |
S32 |
9 | BAA05g12150 | A05 | 6175942 | C | T | upstream_gene_variant | MODIFIER | c.-321G>A| |
S197 |
10 | BAA05g12150 | A05 | 6176461 | C | T | upstream_gene_variant | MODIFIER | c.-840G>A| |
S130 |
11 | BAA05g12150 | A05 | 6176558 | C | T | upstream_gene_variant | MODIFIER | c.-937G>A| |
S198 |
12 | BAA05g12150 | A05 | 6177961 | C | T | upstream_gene_variant | MODIFIER | c.-2340G>A| |
S117 |
13 | BAA05g12150 | A05 | 6179786 | C | T | upstream_gene_variant | MODIFIER | c.-4165G>A| |
S12 |
14 | BAA05g12150 | A05 | 6180117 | C | T | upstream_gene_variant | MODIFIER | c.-4496G>A| |
S251 |
15 | BAA05g12150 | A05 | 6180141 | C | T | upstream_gene_variant | MODIFIER | c.-4520G>A| |
S174 S27 |
16 | BAA05g12150 | A05 | 6180435 | G | A | upstream_gene_variant | MODIFIER | c.-4814C>T| |
S129 |