Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g17580 | A05 | 9904925 | A | T | downstream_gene_variant | MODIFIER | c.*4879T>A| |
S179 |
2 | BAA05g17580 | A05 | 9905356 | C | T | downstream_gene_variant | MODIFIER | c.*4448G>A| |
S71 |
3 | BAA05g17580 | A05 | 9905871 | G | A | downstream_gene_variant | MODIFIER | c.*3933C>T| |
S283 |
4 | BAA05g17580 | A05 | 9906392 | C | T | downstream_gene_variant | MODIFIER | c.*3412G>A| |
S142 |
5 | BAA05g17580 | A05 | 9906684 | G | A | downstream_gene_variant | MODIFIER | c.*3120C>T| |
S282 |
6 | BAA05g17580 | A05 | 9906949 | G | A | downstream_gene_variant | MODIFIER | c.*2855C>T| |
S156 |
7 | BAA05g17580 | A05 | 9907033 | C | T | downstream_gene_variant | MODIFIER | c.*2771G>A| |
S17 |
8 | BAA05g17580 | A05 | 9907490 | C | T | downstream_gene_variant | MODIFIER | c.*2314G>A| |
S216 |
9 | BAA05g17580 | A05 | 9907921 | G | A | downstream_gene_variant | MODIFIER | c.*1883C>T| |
S174 S39 |
10 | BAA05g17580 | A05 | 9907978 | G | A | downstream_gene_variant | MODIFIER | c.*1826C>T| |
S294 |
11 | BAA05g17580 | A05 | 9908127 | C | T | downstream_gene_variant | MODIFIER | c.*1677G>A| |
S255 |
12 | BAA05g17580 | A05 | 9908911 | G | A | downstream_gene_variant | MODIFIER | c.*893C>T| |
S41 |
13 | BAA05g17580 | A05 | 9908957 | C | T | downstream_gene_variant | MODIFIER | c.*847G>A| |
S7 S87 |
14 | BAA05g17580 | A05 | 9909172 | C | T | downstream_gene_variant | MODIFIER | c.*632G>A| |
S271 |
15 | BAA05g17580 | A05 | 9909434 | G | A | downstream_gene_variant | MODIFIER | c.*370C>T| |
S68 |
16 | BAA05g17580 | A05 | 9910494 | G | A | missense_variant | MODERATE | c.38C>T|p.Ser13Leu |
S260 |
17 | BAA05g17580 | A05 | 9913127 | G | A | upstream_gene_variant | MODIFIER | c.-2596C>T| |
S279 |
18 | BAA05g17580 | A05 | 9913674 | G | A | upstream_gene_variant | MODIFIER | c.-3143C>T| |
S86 |