Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g27220 | A01 | 15588525 | G | A | upstream_gene_variant | MODIFIER | c.-4419G>A| |
S138 |
2 | BAA01g27220 | A01 | 15590388 | G | A | upstream_gene_variant | MODIFIER | c.-2556G>A| |
S6 |
3 | BAA01g27220 | A01 | 15590407 | C | T | upstream_gene_variant | MODIFIER | c.-2537C>T| |
S234 |
4 | BAA01g27220 | A01 | 15590450 | C | T | upstream_gene_variant | MODIFIER | c.-2494C>T| |
S136 |
5 | BAA01g27220 | A01 | 15590578 | C | T | upstream_gene_variant | MODIFIER | c.-2366C>T| |
S16 |
6 | BAA01g27220 | A01 | 15590988 | G | A | upstream_gene_variant | MODIFIER | c.-1956G>A| |
S13 |
7 | BAA01g27220 | A01 | 15591220 | C | T | upstream_gene_variant | MODIFIER | c.-1724C>T| |
S76 |
8 | BAA01g27220 | A01 | 15591397 | G | A | upstream_gene_variant | MODIFIER | c.-1547G>A| |
S299 |
9 | BAA01g27220 | A01 | 15593025 | C | T | missense_variant | MODERATE | c.82C>T|p.Pro28Ser |
S135 |
10 | BAA01g27220 | A01 | 15593799 | G | A | missense_variant | MODERATE | c.362G>A|p.Gly121Glu |
S301 S304 |
11 | BAA01g27220 | A01 | 15593845 | C | T | synonymous_variant | LOW | c.408C>T|p.Phe136Phe |
S234 |
12 | BAA01g27220 | A01 | 15597147 | G | A | downstream_gene_variant | MODIFIER | c.*3212G>A| |
S121 |
13 | BAA01g27220 | A01 | 15597334 | C | T | downstream_gene_variant | MODIFIER | c.*3399C>T| |
S231 |
14 | BAA01g27220 | A01 | 15597506 | C | T | downstream_gene_variant | MODIFIER | c.*3571C>T| |
S272 |