Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g29960 | A09 | 20936253 | C | T | upstream_gene_variant | MODIFIER | c.-4266C>T| |
S297 |
2 | BAA09g29960 | A09 | 20937228 | G | A | upstream_gene_variant | MODIFIER | c.-3291G>A| |
S67 |
3 | BAA09g29960 | A09 | 20937416 | C | T | upstream_gene_variant | MODIFIER | c.-3103C>T| |
S256 |
4 | BAA09g29960 | A09 | 20938349 | C | T | upstream_gene_variant | MODIFIER | c.-2170C>T| |
S228 |
5 | BAA09g29960 | A09 | 20938374 | C | T | upstream_gene_variant | MODIFIER | c.-2145C>T| |
S206 S26 |
6 | BAA09g29960 | A09 | 20939271 | C | T | upstream_gene_variant | MODIFIER | c.-1248C>T| |
S200 |
7 | BAA09g29960 | A09 | 20939462 | C | T | upstream_gene_variant | MODIFIER | c.-1057C>T| |
S293 |
8 | BAA09g29960 | A09 | 20940616 | G | A | missense_variant | MODERATE | c.98G>A|p.Arg33Lys |
S184 |
9 | BAA09g29960 | A09 | 20941834 | C | T | stop_gained | HIGH | c.1000C>T|p.Gln334* |
S80 |
10 | BAA09g29960 | A09 | 20942119 | G | A | missense_variant | MODERATE | c.1285G>A|p.Glu429Lys |
S73 S91 |
11 | BAA09g29960 | A09 | 20942653 | G | A | missense_variant | MODERATE | c.1819G>A|p.Glu607Lys |
S62 |
12 | BAA09g29960 | A09 | 20943761 | C | T | downstream_gene_variant | MODIFIER | c.*692C>T| |
S57 |
13 | BAA09g29960 | A09 | 20944701 | C | T | downstream_gene_variant | MODIFIER | c.*1632C>T| |
S174 |
14 | BAA09g29960 | A09 | 20945430 | C | A | downstream_gene_variant | MODIFIER | c.*2361C>A| |
S126 |
15 | BAA09g29960 | A09 | 20945459 | C | T | downstream_gene_variant | MODIFIER | c.*2390C>T| |
S188 |
16 | BAA09g29960 | A09 | 20946283 | C | T | downstream_gene_variant | MODIFIER | c.*3214C>T| |
S256 S32 |
17 | BAA09g29960 | A09 | 20946359 | C | T | downstream_gene_variant | MODIFIER | c.*3290C>T| |
S172 S217 |
18 | BAA09g29960 | A09 | 20946884 | C | T | downstream_gene_variant | MODIFIER | c.*3815C>T| |
S294 |
19 | BAA09g29960 | A09 | 20947000 | C | T | downstream_gene_variant | MODIFIER | c.*3931C>T| |
S117 |
20 | BAA09g29960 | A09 | 20947078 | C | T | downstream_gene_variant | MODIFIER | c.*4009C>T| |
S144 |
21 | BAA09g29960 | A09 | 20947910 | C | T | downstream_gene_variant | MODIFIER | c.*4841C>T| |
S143 |