Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g42660 | A02 | 35513219 | T | C | upstream_gene_variant | MODIFIER | c.-1329T>C| |
S274 |
2 | BAA02g42660 | A02 | 35513580 | C | T | upstream_gene_variant | MODIFIER | c.-968C>T| |
S3 |
3 | BAA02g42660 | A02 | 35513645 | C | T | upstream_gene_variant | MODIFIER | c.-903C>T| |
S109 |
4 | BAA02g42660 | A02 | 35514575 | T | C | missense_variant | MODERATE | c.28T>C|p.Tyr10His |
S26 |
5 | BAA02g42660 | A02 | 35515126 | C | T | missense_variant | MODERATE | c.398C>T|p.Ser133Leu |
S42 |
6 | BAA02g42660 | A02 | 35516737 | G | A | downstream_gene_variant | MODIFIER | c.*1562G>A| |
S177 |
7 | BAA02g42660 | A02 | 35516976 | C | T | downstream_gene_variant | MODIFIER | c.*1801C>T| |
S172 |
8 | BAA02g42660 | A02 | 35516980 | C | T | downstream_gene_variant | MODIFIER | c.*1805C>T| |
S295 |
9 | BAA02g42660 | A02 | 35517532 | C | T | downstream_gene_variant | MODIFIER | c.*2357C>T| |
S179 |
10 | BAA02g42660 | A02 | 35519654 | C | T | downstream_gene_variant | MODIFIER | c.*4479C>T| |
S112 |