Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g48250 | A02 | 38740487 | G | A | upstream_gene_variant | MODIFIER | c.-2694G>A| |
S132 S137 S215 |
2 | BAA02g48250 | A02 | 38741007 | C | T | upstream_gene_variant | MODIFIER | c.-2174C>T| |
S48 |
3 | BAA02g48250 | A02 | 38741396 | C | T | upstream_gene_variant | MODIFIER | c.-1785C>T| |
S176 |
4 | BAA02g48250 | A02 | 38741730 | G | A | upstream_gene_variant | MODIFIER | c.-1451G>A| |
S259 |
5 | BAA02g48250 | A02 | 38743085 | C | T | upstream_gene_variant | MODIFIER | c.-96C>T| |
S135 |
6 | BAA02g48250 | A02 | 38743837 | G | A | missense_variant | MODERATE | c.508G>A|p.Val170Ile |
S94 |
7 | BAA02g48250 | A02 | 38744966 | C | T | intron_variant | MODIFIER | c.1295+29C>T| |
S260 |
8 | BAA02g48250 | A02 | 38745437 | G | A | missense_variant | MODERATE | c.1547G>A|p.Arg516His |
S105 S106 |
9 | BAA02g48250 | A02 | 38745846 | G | A | synonymous_variant | LOW | c.1749G>A|p.Leu583Leu |
S281 |
10 | BAA02g48250 | A02 | 38745857 | C | T | missense_variant | MODERATE | c.1760C>T|p.Ser587Phe |
S138 |
11 | BAA02g48250 | A02 | 38746704 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.2155-1G>A| |
S56 |
12 | BAA02g48250 | A02 | 38747262 | G | A | missense_variant | MODERATE | c.2498G>A|p.Arg833Lys |
S144 |
13 | BAA02g48250 | A02 | 38749076 | C | T | missense_variant | MODERATE | c.3620C>T|p.Ser1207Phe |
S303 |
14 | BAA02g48250 | A02 | 38749120 | G | A | missense_variant | MODERATE | c.3664G>A|p.Glu1222Lys |
S205 |
15 | BAA02g48250 | A02 | 38749828 | C | T | downstream_gene_variant | MODIFIER | c.*625C>T| |
S182 |
16 | BAA02g48250 | A02 | 38750266 | C | T | downstream_gene_variant | MODIFIER | c.*1063C>T| |
S6 |