Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g12290 | A10 | 13735596 | C | T | upstream_gene_variant | MODIFIER | c.-4754C>T| |
S151 S263 |
2 | BAA10g12290 | A10 | 13735774 | C | T | upstream_gene_variant | MODIFIER | c.-4576C>T| |
S123 |
3 | BAA10g12290 | A10 | 13735944 | G | A | upstream_gene_variant | MODIFIER | c.-4406G>A| |
S74 |
4 | BAA10g12290 | A10 | 13737243 | C | T | upstream_gene_variant | MODIFIER | c.-3107C>T| |
S180 |
5 | BAA10g12290 | A10 | 13737960 | C | T | upstream_gene_variant | MODIFIER | c.-2390C>T| |
S183 |
6 | BAA10g12290 | A10 | 13738727 | G | A | upstream_gene_variant | MODIFIER | c.-1623G>A| |
S72 |
7 | BAA10g12290 | A10 | 13739592 | G | A | upstream_gene_variant | MODIFIER | c.-758G>A| |
S82 S92 |
8 | BAA10g12290 | A10 | 13739738 | G | A | upstream_gene_variant | MODIFIER | c.-612G>A| |
S95 |
9 | BAA10g12290 | A10 | 13739976 | G | A | upstream_gene_variant | MODIFIER | c.-374G>A| |
S208 |
10 | BAA10g12290 | A10 | 13740306 | C | T | upstream_gene_variant | MODIFIER | c.-44C>T| |
S225 S73 |
11 | BAA10g12290 | A10 | 13741167 | G | A | missense_variant | MODERATE | c.469G>A|p.Gly157Arg |
S163 |
12 | BAA10g12290 | A10 | 13741258 | C | T | missense_variant | MODERATE | c.560C>T|p.Pro187Leu |
S210 S225 |
13 | BAA10g12290 | A10 | 13741285 | G | A | missense_variant | MODERATE | c.587G>A|p.Gly196Asp |
S250 |
14 | BAA10g12290 | A10 | 13744057 | G | A | downstream_gene_variant | MODIFIER | c.*2158G>A| |
S290 |
15 | BAA10g12290 | A10 | 13744819 | C | T | downstream_gene_variant | MODIFIER | c.*2920C>T| |
S25 |