Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g10240 | A10 | 12013368 | C | T | downstream_gene_variant | MODIFIER | c.*858G>A| |
S236 |
2 | BAA10g10240 | A10 | 12013832 | C | T | downstream_gene_variant | MODIFIER | c.*394G>A| |
S256 |
3 | BAA10g10240 | A10 | 12014075 | C | T | downstream_gene_variant | MODIFIER | c.*151G>A| |
S174 S27 |
4 | BAA10g10240 | A10 | 12014395 | C | T | intron_variant | MODIFIER | c.514-26G>A| |
S177 |
5 | BAA10g10240 | A10 | 12019625 | G | A | missense_variant | MODERATE | c.179C>T|p.Ser60Phe |
S289 |
6 | BAA10g10240 | A10 | 12019909 | G | A | upstream_gene_variant | MODIFIER | c.-106C>T| |
S69 |
7 | BAA10g10240 | A10 | 12020065 | G | A | upstream_gene_variant | MODIFIER | c.-262C>T| |
S13 |
8 | BAA10g10240 | A10 | 12020256 | G | A | upstream_gene_variant | MODIFIER | c.-453C>T| |
S71 |
9 | BAA10g10240 | A10 | 12020596 | C | T | upstream_gene_variant | MODIFIER | c.-793G>A| |
S152 |
10 | BAA10g10240 | A10 | 12021004 | C | T | upstream_gene_variant | MODIFIER | c.-1201G>A| |
S46 |
11 | BAA10g10240 | A10 | 12022030 | G | A | upstream_gene_variant | MODIFIER | c.-2227C>T| |
S240 |
12 | BAA10g10240 | A10 | 12022141 | C | T | upstream_gene_variant | MODIFIER | c.-2338G>A| |
S187 |
13 | BAA10g10240 | A10 | 12022828 | G | A | upstream_gene_variant | MODIFIER | c.-3025C>T| |
S78 |
14 | BAA10g10240 | A10 | 12024522 | C | T | upstream_gene_variant | MODIFIER | c.-4719G>A| |
S260 |