Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g20180 | A10 | 18254993 | G | T | upstream_gene_variant | MODIFIER | c.-4523G>T| |
S117 |
2 | BAA10g20180 | A10 | 18256592 | C | T | upstream_gene_variant | MODIFIER | c.-2924C>T| |
S246 |
3 | BAA10g20180 | A10 | 18256739 | C | T | upstream_gene_variant | MODIFIER | c.-2777C>T| |
S5 |
4 | BAA10g20180 | A10 | 18258133 | G | A | upstream_gene_variant | MODIFIER | c.-1383G>A| |
S293 |
5 | BAA10g20180 | A10 | 18258820 | C | T | upstream_gene_variant | MODIFIER | c.-696C>T| |
S69 |
6 | BAA10g20180 | A10 | 18258861 | G | A | upstream_gene_variant | MODIFIER | c.-655G>A| |
S155 S211 |
7 | BAA10g20180 | A10 | 18259104 | G | A | upstream_gene_variant | MODIFIER | c.-412G>A| |
S233 |
8 | BAA10g20180 | A10 | 18261382 | G | A | missense_variant | MODERATE | c.892G>A|p.Ala298Thr |
S179 |
9 | BAA10g20180 | A10 | 18262668 | C | T | downstream_gene_variant | MODIFIER | c.*1148C>T| |
S296 |
10 | BAA10g20180 | A10 | 18262790 | C | T | downstream_gene_variant | MODIFIER | c.*1270C>T| |
S186 |
11 | BAA10g20180 | A10 | 18264052 | G | A | downstream_gene_variant | MODIFIER | c.*2532G>A| |
S233 |
12 | BAA10g20180 | A10 | 18265099 | G | A | downstream_gene_variant | MODIFIER | c.*3579G>A| |
S237 |
13 | BAA10g20180 | A10 | 18265375 | G | A | downstream_gene_variant | MODIFIER | c.*3855G>A| |
S239 |
14 | BAA10g20180 | A10 | 18265602 | G | A | downstream_gene_variant | MODIFIER | c.*4082G>A| |
S143 |