Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g43580 | A02 | 36076448 | G | A | upstream_gene_variant | MODIFIER | c.-4447G>A| |
S69 |
2 | BAA02g43580 | A02 | 36076991 | C | T | upstream_gene_variant | MODIFIER | c.-3904C>T| |
S19 |
3 | BAA02g43580 | A02 | 36077506 | G | A | upstream_gene_variant | MODIFIER | c.-3389G>A| |
S43 |
4 | BAA02g43580 | A02 | 36081084 | C | T | synonymous_variant | LOW | c.79C>T|p.Leu27Leu |
S172 |
5 | BAA02g43580 | A02 | 36081971 | G | A | intron_variant | MODIFIER | c.495+113G>A| |
S229 |
6 | BAA02g43580 | A02 | 36082117 | C | T | missense_variant | MODERATE | c.526C>T|p.Leu176Phe |
S171 |
7 | BAA02g43580 | A02 | 36082397 | G | A | intron_variant | MODIFIER | c.657+54G>A| |
S209 |
8 | BAA02g43580 | A02 | 36082541 | G | A | missense_variant | MODERATE | c.698G>A|p.Arg233Lys |
S132 S137 S215 |
9 | BAA02g43580 | A02 | 36082967 | C | T | missense_variant | MODERATE | c.886C>T|p.Pro296Ser |
S234 |
10 | BAA02g43580 | A02 | 36083480 | C | T | intron_variant | MODIFIER | c.966+433C>T| |
S1 S90 |
11 | BAA02g43580 | A02 | 36083508 | C | T | intron_variant | MODIFIER | c.966+461C>T| |
S263 |
12 | BAA02g43580 | A02 | 36084790 | G | A | splice_region_variant&intron_variant | LOW | c.1238-7G>A| |
S168 |
13 | BAA02g43580 | A02 | 36086110 | C | T | splice_region_variant&intron_variant | LOW | c.1720-7C>T| |
S97 |
14 | BAA02g43580 | A02 | 36088018 | C | T | downstream_gene_variant | MODIFIER | c.*1716C>T| |
S171 |
15 | BAA02g43580 | A02 | 36088216 | C | T | downstream_gene_variant | MODIFIER | c.*1914C>T| |
S272 |
16 | BAA02g43580 | A02 | 36088475 | C | T | downstream_gene_variant | MODIFIER | c.*2173C>T| |
S16 |
17 | BAA02g43580 | A02 | 36089731 | C | T | downstream_gene_variant | MODIFIER | c.*3429C>T| |
S117 |
18 | BAA02g43580 | A02 | 36090538 | G | A | downstream_gene_variant | MODIFIER | c.*4236G>A| |
S210 |