Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g17290 | A02 | 8610050 | G | A | upstream_gene_variant | MODIFIER | c.-4934G>A| |
S153 S213 |
2 | BAA02g17290 | A02 | 8611662 | C | T | upstream_gene_variant | MODIFIER | c.-3322C>T| |
S63 |
3 | BAA02g17290 | A02 | 8611784 | G | A | upstream_gene_variant | MODIFIER | c.-3200G>A| |
S240 |
4 | BAA02g17290 | A02 | 8611847 | G | A | upstream_gene_variant | MODIFIER | c.-3137G>A| |
S240 |
5 | BAA02g17290 | A02 | 8612669 | C | T | upstream_gene_variant | MODIFIER | c.-2315C>T| |
S88 |
6 | BAA02g17290 | A02 | 8612812 | G | A | upstream_gene_variant | MODIFIER | c.-2172G>A| |
S223 |
7 | BAA02g17290 | A02 | 8612821 | C | T | upstream_gene_variant | MODIFIER | c.-2163C>T| |
S144 |
8 | BAA02g17290 | A02 | 8613078 | G | A | upstream_gene_variant | MODIFIER | c.-1906G>A| |
S187 |
9 | BAA02g17290 | A02 | 8613413 | G | A | upstream_gene_variant | MODIFIER | c.-1571G>A| |
S202 |
10 | BAA02g17290 | A02 | 8615650 | C | T | missense_variant | MODERATE | c.401C>T|p.Pro134Leu |
S160 |
11 | BAA02g17290 | A02 | 8616645 | C | T | missense_variant | MODERATE | c.863C>T|p.Pro288Leu |
S200 |
12 | BAA02g17290 | A02 | 8617026 | G | A | missense_variant | MODERATE | c.1000G>A|p.Asp334Asn |
S303 |
13 | BAA02g17290 | A02 | 8620939 | G | A | downstream_gene_variant | MODIFIER | c.*2649G>A| |
S20 |