Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g22660 | A02 | 12278963 | G | A | downstream_gene_variant | MODIFIER | c.*4237C>T| |
S148 S210 |
2 | BAA02g22660 | A02 | 12283372 | G | A | missense_variant | MODERATE | c.205C>T|p.Pro69Ser |
S45 |
3 | BAA02g22660 | A02 | 12283537 | C | T | missense_variant | MODERATE | c.40G>A|p.Val14Met |
S170 |
4 | BAA02g22660 | A02 | 12283544 | C | T | synonymous_variant | LOW | c.33G>A|p.Gln11Gln |
S85 |
5 | BAA02g22660 | A02 | 12286164 | G | A | upstream_gene_variant | MODIFIER | c.-2588C>T| |
S17 |
6 | BAA02g22660 | A02 | 12286189 | G | A | upstream_gene_variant | MODIFIER | c.-2613C>T| |
S37 |
7 | BAA02g22660 | A02 | 12286594 | G | A | upstream_gene_variant | MODIFIER | c.-3018C>T| |
S72 S78 |
8 | BAA02g22660 | A02 | 12286720 | C | T | upstream_gene_variant | MODIFIER | c.-3144G>A| |
S305 |
9 | BAA02g22660 | A02 | 12287197 | C | T | upstream_gene_variant | MODIFIER | c.-3621G>A| |
S65 |
10 | BAA02g22660 | A02 | 12287200 | C | T | upstream_gene_variant | MODIFIER | c.-3624G>A| |
S255 |