Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g10880 | A02 | 4864254 | C | T | synonymous_variant | LOW | c.2076G>A|p.Lys692Lys |
S142 |
2 | BAA02g10880 | A02 | 4866121 | A | G | synonymous_variant | LOW | c.774T>C|p.Asp258Asp |
S152 |
3 | BAA02g10880 | A02 | 4866510 | G | A | intron_variant | MODIFIER | c.489-16C>T| |
S259 |
4 | BAA02g10880 | A02 | 4866614 | C | T | missense_variant | MODERATE | c.451G>A|p.Gly151Ser |
S193 |
5 | BAA02g10880 | A02 | 4867423 | C | T | missense_variant | MODERATE | c.137G>A|p.Ser46Asn |
S131 |
6 | BAA02g10880 | A02 | 4867690 | G | A | upstream_gene_variant | MODIFIER | c.-131C>T| |
S104 |
7 | BAA02g10880 | A02 | 4867733 | C | T | upstream_gene_variant | MODIFIER | c.-174G>A| |
S135 |
8 | BAA02g10880 | A02 | 4869922 | C | T | upstream_gene_variant | MODIFIER | c.-2363G>A| |
S208 |
9 | BAA02g10880 | A02 | 4870617 | G | A | upstream_gene_variant | MODIFIER | c.-3058C>T| |
S146 |
10 | BAA02g10880 | A02 | 4870701 | C | T | upstream_gene_variant | MODIFIER | c.-3142G>A| |
S172 S217 |
11 | BAA02g10880 | A02 | 4871089 | G | A | upstream_gene_variant | MODIFIER | c.-3530C>T| |
S9 |
12 | BAA02g10880 | A02 | 4871197 | C | T | upstream_gene_variant | MODIFIER | c.-3638G>A| |
S289 S290 |
13 | BAA02g10880 | A02 | 4871834 | G | A | upstream_gene_variant | MODIFIER | c.-4275C>T| |
S192 |