Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g04190 | A10 | 2104673 | G | A | upstream_gene_variant | MODIFIER | c.-4808G>A| |
S172 S217 |
2 | BAA10g04190 | A10 | 2106805 | G | A | upstream_gene_variant | MODIFIER | c.-2676G>A| |
S263 |
3 | BAA10g04190 | A10 | 2106863 | G | A | upstream_gene_variant | MODIFIER | c.-2618G>A| |
S16 |
4 | BAA10g04190 | A10 | 2106958 | C | T | upstream_gene_variant | MODIFIER | c.-2523C>T| |
S203 |
5 | BAA10g04190 | A10 | 2108021 | G | A | upstream_gene_variant | MODIFIER | c.-1460G>A| |
S180 |
6 | BAA10g04190 | A10 | 2108074 | C | T | upstream_gene_variant | MODIFIER | c.-1407C>T| |
S281 |
7 | BAA10g04190 | A10 | 2108220 | G | A | upstream_gene_variant | MODIFIER | c.-1261G>A| |
S245 |
8 | BAA10g04190 | A10 | 2108549 | C | T | upstream_gene_variant | MODIFIER | c.-932C>T| |
S252 |
9 | BAA10g04190 | A10 | 2108703 | G | A | upstream_gene_variant | MODIFIER | c.-778G>A| |
S90 |
10 | BAA10g04190 | A10 | 2108832 | C | T | upstream_gene_variant | MODIFIER | c.-649C>T| |
S270 |
11 | BAA10g04190 | A10 | 2108833 | C | T | upstream_gene_variant | MODIFIER | c.-648C>T| |
S136 S186 |
12 | BAA10g04190 | A10 | 2109290 | G | A | upstream_gene_variant | MODIFIER | c.-191G>A| |
S245 |
13 | BAA10g04190 | A10 | 2110147 | C | T | downstream_gene_variant | MODIFIER | c.*511C>T| |
S135 |
14 | BAA10g04190 | A10 | 2110700 | C | T | downstream_gene_variant | MODIFIER | c.*1064C>T| |
S308 |
15 | BAA10g04190 | A10 | 2111258 | T | A | downstream_gene_variant | MODIFIER | c.*1622T>A| |
S108 |
16 | BAA10g04190 | A10 | 2111541 | G | A | downstream_gene_variant | MODIFIER | c.*1905G>A| |
S282 |