Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g28690 | A03 | 13306231 | C | T | upstream_gene_variant | MODIFIER | c.-2093C>T| |
S176 |
2 | BAA03g28690 | A03 | 13306910 | G | A | upstream_gene_variant | MODIFIER | c.-1414G>A| |
S149 S176 |
3 | BAA03g28690 | A03 | 13308420 | G | A | missense_variant | MODERATE | c.97G>A|p.Ala33Thr |
S109 |
4 | BAA03g28690 | A03 | 13308447 | C | T | missense_variant | MODERATE | c.124C>T|p.Pro42Ser |
S132 S137 S215 S287 S89 |
5 | BAA03g28690 | A03 | 13310042 | G | A | stop_gained | HIGH | c.939G>A|p.Trp313* |
S12 |
6 | BAA03g28690 | A03 | 13310112 | C | T | missense_variant | MODERATE | c.1009C>T|p.Leu337Phe |
S211 S227 |
7 | BAA03g28690 | A03 | 13313094 | G | A | downstream_gene_variant | MODIFIER | c.*2902G>A| |
S203 |
8 | BAA03g28690 | A03 | 13313102 | C | T | downstream_gene_variant | MODIFIER | c.*2910C>T| |
S18 |
9 | BAA03g28690 | A03 | 13313638 | G | A | downstream_gene_variant | MODIFIER | c.*3446G>A| |
S260 |
10 | BAA03g28690 | A03 | 13314570 | C | T | downstream_gene_variant | MODIFIER | c.*4378C>T| |
S120 |
11 | BAA03g28690 | A03 | 13314894 | G | A | downstream_gene_variant | MODIFIER | c.*4702G>A| |
S296 |
12 | BAA03g28690 | A03 | 13315101 | G | A | downstream_gene_variant | MODIFIER | c.*4909G>A| |
S133 |