Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g10740 | A05 | 5486876 | G | A | downstream_gene_variant | MODIFIER | c.*4590C>T| |
S132 S137 S215 S89 |
2 | BAA05g10740 | A05 | 5487307 | G | A | downstream_gene_variant | MODIFIER | c.*4159C>T| |
S218 |
3 | BAA05g10740 | A05 | 5487877 | G | A | downstream_gene_variant | MODIFIER | c.*3589C>T| |
S240 |
4 | BAA05g10740 | A05 | 5488078 | G | A | downstream_gene_variant | MODIFIER | c.*3388C>T| |
S274 |
5 | BAA05g10740 | A05 | 5488126 | G | A | downstream_gene_variant | MODIFIER | c.*3340C>T| |
S294 |
6 | BAA05g10740 | A05 | 5488419 | C | T | downstream_gene_variant | MODIFIER | c.*3047G>A| |
S270 |
7 | BAA05g10740 | A05 | 5489201 | G | A | downstream_gene_variant | MODIFIER | c.*2265C>T| |
S131 S221 |
8 | BAA05g10740 | A05 | 5489307 | G | A | downstream_gene_variant | MODIFIER | c.*2159C>T| |
S294 |
9 | BAA05g10740 | A05 | 5489348 | G | A | downstream_gene_variant | MODIFIER | c.*2118C>T| |
S293 |
10 | BAA05g10740 | A05 | 5489662 | G | A | downstream_gene_variant | MODIFIER | c.*1804C>T| |
S289 |
11 | BAA05g10740 | A05 | 5489755 | C | T | downstream_gene_variant | MODIFIER | c.*1711G>A| |
S233 |
12 | BAA05g10740 | A05 | 5491008 | G | A | downstream_gene_variant | MODIFIER | c.*458C>T| |
S134 |
13 | BAA05g10740 | A05 | 5491182 | G | A | downstream_gene_variant | MODIFIER | c.*284C>T| |
S296 S46 |
14 | BAA05g10740 | A05 | 5493568 | C | T | upstream_gene_variant | MODIFIER | c.-1836G>A| |
S143 |
15 | BAA05g10740 | A05 | 5493947 | C | T | upstream_gene_variant | MODIFIER | c.-2215G>A| |
S35 |
16 | BAA05g10740 | A05 | 5494222 | G | A | upstream_gene_variant | MODIFIER | c.-2490C>T| |
S115 |
17 | BAA05g10740 | A05 | 5494865 | C | T | upstream_gene_variant | MODIFIER | c.-3133G>A| |
S232 S84 |
18 | BAA05g10740 | A05 | 5495996 | G | A | upstream_gene_variant | MODIFIER | c.-4264C>T| |
S226 |
19 | BAA05g10740 | A05 | 5496013 | C | T | upstream_gene_variant | MODIFIER | c.-4281G>A| |
S99 |
20 | BAA05g10740 | A05 | 5496440 | C | T | upstream_gene_variant | MODIFIER | c.-4708G>A| |
S245 |