Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g27010 | A01 | 15311261 | C | T | downstream_gene_variant | MODIFIER | c.*2658G>A| |
S7 |
2 | BAA01g27010 | A01 | 15312552 | G | A | downstream_gene_variant | MODIFIER | c.*1367C>T| |
S172 S217 |
3 | BAA01g27010 | A01 | 15312589 | G | A | downstream_gene_variant | MODIFIER | c.*1330C>T| |
S191 |
4 | BAA01g27010 | A01 | 15312687 | C | A | downstream_gene_variant | MODIFIER | c.*1232G>T| |
S213 |
5 | BAA01g27010 | A01 | 15312918 | C | T | downstream_gene_variant | MODIFIER | c.*1001G>A| |
S128 |
6 | BAA01g27010 | A01 | 15313146 | C | T | downstream_gene_variant | MODIFIER | c.*773G>A| |
S96 |
7 | BAA01g27010 | A01 | 15313549 | C | T | downstream_gene_variant | MODIFIER | c.*370G>A| |
S113 |
8 | BAA01g27010 | A01 | 15313800 | C | T | downstream_gene_variant | MODIFIER | c.*119G>A| |
S66 |
9 | BAA01g27010 | A01 | 15314331 | C | T | intron_variant | MODIFIER | c.3571-29G>A| |
S41 |
10 | BAA01g27010 | A01 | 15315075 | G | A | missense_variant | MODERATE | c.3058C>T|p.Leu1020Phe |
S292 |
11 | BAA01g27010 | A01 | 15315162 | C | T | intron_variant | MODIFIER | c.3008-37G>A| |
S182 |
12 | BAA01g27010 | A01 | 15315453 | G | A | intron_variant | MODIFIER | c.2959-36C>T| |
S308 |
13 | BAA01g27010 | A01 | 15315955 | G | A | intron_variant | MODIFIER | c.2959-538C>T| |
S105 S106 |
14 | BAA01g27010 | A01 | 15316040 | G | A | intron_variant | MODIFIER | c.2959-623C>T| |
S207 |
15 | BAA01g27010 | A01 | 15316542 | C | T | intron_variant | MODIFIER | c.2959-1125G>A| |
S114 |
16 | BAA01g27010 | A01 | 15316923 | C | T | intron_variant | MODIFIER | c.2959-1506G>A| |
S267 |
17 | BAA01g27010 | A01 | 15316967 | C | T | intron_variant | MODIFIER | c.2959-1550G>A| |
S10 |
18 | BAA01g27010 | A01 | 15317259 | G | A | intron_variant | MODIFIER | c.2958+1418C>T| |
S268 |
19 | BAA01g27010 | A01 | 15317482 | G | A | intron_variant | MODIFIER | c.2958+1195C>T| |
S68 |
20 | BAA01g27010 | A01 | 15317693 | C | T | intron_variant | MODIFIER | c.2958+984G>A| |
S51 |
21 | BAA01g27010 | A01 | 15318157 | C | T | intron_variant | MODIFIER | c.2958+520G>A| |
S213 |
22 | BAA01g27010 | A01 | 15318163 | C | T | intron_variant | MODIFIER | c.2958+514G>A| |
S184 |
23 | BAA01g27010 | A01 | 15318197 | G | A | intron_variant | MODIFIER | c.2958+480C>T| |
S308 |
24 | BAA01g27010 | A01 | 15319558 | C | T | missense_variant | MODERATE | c.2077G>A|p.Asp693Asn |
S231 |
25 | BAA01g27010 | A01 | 15319789 | C | T | missense_variant | MODERATE | c.1846G>A|p.Val616Ile |
S64 |