Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g14610 | A10 | 15251112 | G | A | downstream_gene_variant | MODIFIER | c.*4926C>T| |
S65 |
2 | BAA10g14610 | A10 | 15251771 | C | T | downstream_gene_variant | MODIFIER | c.*4267G>A| |
S225 S73 |
3 | BAA10g14610 | A10 | 15252360 | C | T | downstream_gene_variant | MODIFIER | c.*3678G>A| |
S115 |
4 | BAA10g14610 | A10 | 15252508 | G | A | downstream_gene_variant | MODIFIER | c.*3530C>T| |
S286 |
5 | BAA10g14610 | A10 | 15252613 | G | A | downstream_gene_variant | MODIFIER | c.*3425C>T| |
S203 |
6 | BAA10g14610 | A10 | 15254806 | G | A | downstream_gene_variant | MODIFIER | c.*1232C>T| |
S159 S243 |
7 | BAA10g14610 | A10 | 15255064 | G | A | downstream_gene_variant | MODIFIER | c.*974C>T| |
S109 |
8 | BAA10g14610 | A10 | 15255148 | G | A | downstream_gene_variant | MODIFIER | c.*890C>T| |
S208 |
9 | BAA10g14610 | A10 | 15255224 | G | A | downstream_gene_variant | MODIFIER | c.*814C>T| |
S207 |
10 | BAA10g14610 | A10 | 15255501 | C | T | downstream_gene_variant | MODIFIER | c.*537G>A| |
S156 |
11 | BAA10g14610 | A10 | 15255959 | C | T | downstream_gene_variant | MODIFIER | c.*79G>A| |
S156 |
12 | BAA10g14610 | A10 | 15256371 | C | T | missense_variant | MODERATE | c.162G>A|p.Met54Ile |
S256 |
13 | BAA10g14610 | A10 | 15256805 | G | A | upstream_gene_variant | MODIFIER | c.-273C>T| |
S262 |
14 | BAA10g14610 | A10 | 15257192 | G | A | upstream_gene_variant | MODIFIER | c.-660C>T| |
S164 |
15 | BAA10g14610 | A10 | 15257515 | C | T | upstream_gene_variant | MODIFIER | c.-983G>A| |
S124 |
16 | BAA10g14610 | A10 | 15257540 | C | T | upstream_gene_variant | MODIFIER | c.-1008G>A| |
S247 |
17 | BAA10g14610 | A10 | 15257589 | C | T | upstream_gene_variant | MODIFIER | c.-1057G>A| |
S276 |
18 | BAA10g14610 | A10 | 15258066 | C | T | upstream_gene_variant | MODIFIER | c.-1534G>A| |
S7 |
19 | BAA10g14610 | A10 | 15261402 | C | T | upstream_gene_variant | MODIFIER | c.-4870G>A| |
S175 |