Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g28540 | A02 | 16042411 | C | T | upstream_gene_variant | MODIFIER | c.-4976C>T| |
S219 |
2 | BAA02g28540 | A02 | 16043287 | G | A | upstream_gene_variant | MODIFIER | c.-4100G>A| |
S127 |
3 | BAA02g28540 | A02 | 16043629 | G | A | upstream_gene_variant | MODIFIER | c.-3758G>A| |
S240 |
4 | BAA02g28540 | A02 | 16043889 | G | A | upstream_gene_variant | MODIFIER | c.-3498G>A| |
S38 |
5 | BAA02g28540 | A02 | 16044685 | C | T | upstream_gene_variant | MODIFIER | c.-2702C>T| |
S18 |
6 | BAA02g28540 | A02 | 16045416 | A | T | upstream_gene_variant | MODIFIER | c.-1971A>T| |
S61 |
7 | BAA02g28540 | A02 | 16046144 | C | T | upstream_gene_variant | MODIFIER | c.-1243C>T| |
S104 S52 |
8 | BAA02g28540 | A02 | 16046396 | C | T | upstream_gene_variant | MODIFIER | c.-991C>T| |
S25 S264 |
9 | BAA02g28540 | A02 | 16047246 | C | T | upstream_gene_variant | MODIFIER | c.-141C>T| |
S234 |
10 | BAA02g28540 | A02 | 16047504 | C | T | missense_variant | MODERATE | c.118C>T|p.Pro40Ser |
S293 |
11 | BAA02g28540 | A02 | 16047784 | C | T | missense_variant | MODERATE | c.398C>T|p.Thr133Ile |
S9 |
12 | BAA02g28540 | A02 | 16048489 | G | A | missense_variant | MODERATE | c.932G>A|p.Gly311Asp |
S13 S140 S168 S279 S64 |
13 | BAA02g28540 | A02 | 16048582 | C | T | missense_variant | MODERATE | c.1025C>T|p.Ser342Phe |
S9 |
14 | BAA02g28540 | A02 | 16048759 | G | A | missense_variant | MODERATE | c.1202G>A|p.Gly401Glu |
S5 |
15 | BAA02g28540 | A02 | 16049181 | G | A | missense_variant | MODERATE | c.1624G>A|p.Gly542Ser |
S80 |
16 | BAA02g28540 | A02 | 16049219 | G | A | synonymous_variant | LOW | c.1662G>A|p.Ala554Ala |
S33 |