Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g10590 | A08 | 9514284 | G | A | upstream_gene_variant | MODIFIER | c.-4674G>A| |
S281 |
2 | BAA08g10590 | A08 | 9515236 | C | T | upstream_gene_variant | MODIFIER | c.-3722C>T| |
S142 |
3 | BAA08g10590 | A08 | 9515331 | G | A | upstream_gene_variant | MODIFIER | c.-3627G>A| |
S66 |
4 | BAA08g10590 | A08 | 9516190 | A | T | upstream_gene_variant | MODIFIER | c.-2768A>T| |
S280 |
5 | BAA08g10590 | A08 | 9516486 | C | T | upstream_gene_variant | MODIFIER | c.-2472C>T| |
S70 |
6 | BAA08g10590 | A08 | 9516965 | G | A | upstream_gene_variant | MODIFIER | c.-1993G>A| |
S249 |
7 | BAA08g10590 | A08 | 9517434 | G | A | upstream_gene_variant | MODIFIER | c.-1524G>A| |
S94 |
8 | BAA08g10590 | A08 | 9517752 | C | T | upstream_gene_variant | MODIFIER | c.-1206C>T| |
S261 |
9 | BAA08g10590 | A08 | 9519148 | C | T | missense_variant | MODERATE | c.106C>T|p.Leu36Phe |
S201 |