Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g18020 | A01 | 8816927 | G | A | upstream_gene_variant | MODIFIER | c.-4924G>A| |
S12 |
2 | BAA01g18020 | A01 | 8818257 | G | A | upstream_gene_variant | MODIFIER | c.-3594G>A| |
S201 |
3 | BAA01g18020 | A01 | 8819088 | G | A | upstream_gene_variant | MODIFIER | c.-2763G>A| |
S32 |
4 | BAA01g18020 | A01 | 8819504 | G | A | upstream_gene_variant | MODIFIER | c.-2347G>A| |
S38 |
5 | BAA01g18020 | A01 | 8820074 | G | A | upstream_gene_variant | MODIFIER | c.-1777G>A| |
S105 S106 |
6 | BAA01g18020 | A01 | 8820085 | C | T | upstream_gene_variant | MODIFIER | c.-1766C>T| |
S213 |
7 | BAA01g18020 | A01 | 8820101 | G | A | upstream_gene_variant | MODIFIER | c.-1750G>A| |
S235 |
8 | BAA01g18020 | A01 | 8821044 | G | A | upstream_gene_variant | MODIFIER | c.-807G>A| |
S280 |
9 | BAA01g18020 | A01 | 8822563 | C | T | missense_variant | MODERATE | c.269C>T|p.Thr90Ile |
S50 |
10 | BAA01g18020 | A01 | 8823464 | G | A | synonymous_variant | LOW | c.777G>A|p.Glu259Glu |
S203 |
11 | BAA01g18020 | A01 | 8827716 | T | A | downstream_gene_variant | MODIFIER | c.*3544T>A| |
S33 |
12 | BAA01g18020 | A01 | 8828635 | C | T | downstream_gene_variant | MODIFIER | c.*4463C>T| |
S18 |