Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g09980 | A04 | 16201745 | T | C | upstream_gene_variant | MODIFIER | c.-4244T>C| |
S302 |
2 | BAA04g09980 | A04 | 16202728 | G | A | upstream_gene_variant | MODIFIER | c.-3261G>A| |
S74 |
3 | BAA04g09980 | A04 | 16203387 | G | A | upstream_gene_variant | MODIFIER | c.-2602G>A| |
S259 |
4 | BAA04g09980 | A04 | 16203448 | C | T | upstream_gene_variant | MODIFIER | c.-2541C>T| |
S225 |
5 | BAA04g09980 | A04 | 16204709 | G | A | upstream_gene_variant | MODIFIER | c.-1280G>A| |
S152 |
6 | BAA04g09980 | A04 | 16204972 | A | T | upstream_gene_variant | MODIFIER | c.-1017A>T| |
S280 |
7 | BAA04g09980 | A04 | 16205624 | C | T | upstream_gene_variant | MODIFIER | c.-365C>T| |
S95 |
8 | BAA04g09980 | A04 | 16205921 | C | T | upstream_gene_variant | MODIFIER | c.-68C>T| |
S265 |
9 | BAA04g09980 | A04 | 16206214 | G | A | missense_variant | MODERATE | c.226G>A|p.Gly76Ser |
S38 |
10 | BAA04g09980 | A04 | 16206748 | G | A | missense_variant | MODERATE | c.479G>A|p.Gly160Glu |
S195 |
11 | BAA04g09980 | A04 | 16206755 | C | T | synonymous_variant | LOW | c.486C>T|p.Ser162Ser |
S250 |
12 | BAA04g09980 | A04 | 16208139 | C | T | downstream_gene_variant | MODIFIER | c.*160C>T| |
S142 |
13 | BAA04g09980 | A04 | 16209280 | C | T | downstream_gene_variant | MODIFIER | c.*1301C>T| |
S134 |
14 | BAA04g09980 | A04 | 16210076 | C | T | downstream_gene_variant | MODIFIER | c.*2097C>T| |
S20 |