Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g10700 | A05 | 5441855 | C | T | downstream_gene_variant | MODIFIER | c.*4851G>A| |
S295 |
2 | BAA05g10700 | A05 | 5441894 | G | A | downstream_gene_variant | MODIFIER | c.*4812C>T| |
S1 S90 |
3 | BAA05g10700 | A05 | 5442055 | G | A | downstream_gene_variant | MODIFIER | c.*4651C>T| |
S64 |
4 | BAA05g10700 | A05 | 5443778 | G | A | downstream_gene_variant | MODIFIER | c.*2928C>T| |
S288 |
5 | BAA05g10700 | A05 | 5444681 | C | T | downstream_gene_variant | MODIFIER | c.*2025G>A| |
S57 |
6 | BAA05g10700 | A05 | 5446935 | C | T | intron_variant | MODIFIER | c.1573+111G>A| |
S167 |
7 | BAA05g10700 | A05 | 5447139 | G | A | missense_variant | MODERATE | c.1480C>T|p.Pro494Ser |
S132 S180 |
8 | BAA05g10700 | A05 | 5447429 | C | T | intron_variant | MODIFIER | c.1458+17G>A| |
S236 |
9 | BAA05g10700 | A05 | 5447637 | C | T | missense_variant | MODERATE | c.1267G>A|p.Ala423Thr |
S246 |
10 | BAA05g10700 | A05 | 5449448 | C | T | intron_variant | MODIFIER | c.392-342G>A| |
S289 S290 |
11 | BAA05g10700 | A05 | 5450315 | G | A | intron_variant | MODIFIER | c.391+460C>T| |
S32 |
12 | BAA05g10700 | A05 | 5450535 | C | T | intron_variant | MODIFIER | c.391+240G>A| |
S167 |
13 | BAA05g10700 | A05 | 5452118 | C | T | upstream_gene_variant | MODIFIER | c.-953G>A| |
S108 |
14 | BAA05g10700 | A05 | 5452363 | C | T | upstream_gene_variant | MODIFIER | c.-1198G>A| |
S259 |
15 | BAA05g10700 | A05 | 5452483 | C | T | upstream_gene_variant | MODIFIER | c.-1318G>A| |
S105 S106 |
16 | BAA05g10700 | A05 | 5453137 | C | T | upstream_gene_variant | MODIFIER | c.-1972G>A| |
S52 |
17 | BAA05g10700 | A05 | 5453224 | C | T | upstream_gene_variant | MODIFIER | c.-2059G>A| |
S9 |
18 | BAA05g10700 | A05 | 5453694 | C | T | upstream_gene_variant | MODIFIER | c.-2529G>A| |
S281 |
19 | BAA05g10700 | A05 | 5454430 | C | T | upstream_gene_variant | MODIFIER | c.-3265G>A| |
S113 |