Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g04170 | A02 | 1807711 | C | T | missense_variant | MODERATE | c.484G>A|p.Val162Ile |
S202 |
2 | BAA02g04170 | A02 | 1807964 | G | A | synonymous_variant | LOW | c.231C>T|p.Phe77Phe |
S91 |
3 | BAA02g04170 | A02 | 1808056 | C | T | missense_variant | MODERATE | c.139G>A|p.Asp47Asn |
S179 |
4 | BAA02g04170 | A02 | 1808112 | G | A | missense_variant | MODERATE | c.83C>T|p.Ser28Phe |
S149 |
5 | BAA02g04170 | A02 | 1808165 | A | G | synonymous_variant | LOW | c.30T>C|p.Ser10Ser |
S38 |
6 | BAA02g04170 | A02 | 1810086 | G | A | upstream_gene_variant | MODIFIER | c.-1892C>T| |
S110 |
7 | BAA02g04170 | A02 | 1810253 | G | A | upstream_gene_variant | MODIFIER | c.-2059C>T| |
S302 |
8 | BAA02g04170 | A02 | 1811806 | C | T | upstream_gene_variant | MODIFIER | c.-3612G>A| |
S284 |
9 | BAA02g04170 | A02 | 1811855 | G | A | upstream_gene_variant | MODIFIER | c.-3661C>T| |
S157 |
10 | BAA02g04170 | A02 | 1812784 | G | A | upstream_gene_variant | MODIFIER | c.-4590C>T| |
S57 |