Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g48470 | A09 | 52270941 | T | C | upstream_gene_variant | MODIFIER | c.-4511T>C| |
S115 |
2 | BAA09g48470 | A09 | 52271025 | C | T | upstream_gene_variant | MODIFIER | c.-4427C>T| |
S205 |
3 | BAA09g48470 | A09 | 52271230 | G | A | upstream_gene_variant | MODIFIER | c.-4222G>A| |
S288 |
4 | BAA09g48470 | A09 | 52272597 | C | T | upstream_gene_variant | MODIFIER | c.-2855C>T| |
S61 |
5 | BAA09g48470 | A09 | 52272651 | C | T | upstream_gene_variant | MODIFIER | c.-2801C>T| |
S173 |
6 | BAA09g48470 | A09 | 52272834 | T | A | upstream_gene_variant | MODIFIER | c.-2618T>A| |
S298 |
7 | BAA09g48470 | A09 | 52273306 | C | T | upstream_gene_variant | MODIFIER | c.-2146C>T| |
S27 |
8 | BAA09g48470 | A09 | 52275431 | C | A | upstream_gene_variant | MODIFIER | c.-21C>A| |
S64 |
9 | BAA09g48470 | A09 | 52275511 | G | A | stop_gained | HIGH | c.60G>A|p.Trp20* |
S90 |
10 | BAA09g48470 | A09 | 52275938 | G | A | missense_variant | MODERATE | c.406G>A|p.Ala136Thr |
S201 |
11 | BAA09g48470 | A09 | 52275969 | G | A | missense_variant | MODERATE | c.437G>A|p.Gly146Glu |
S308 |
12 | BAA09g48470 | A09 | 52276873 | C | T | missense_variant | MODERATE | c.598C>T|p.Pro200Ser |
S6 |