Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g00760 | A05 | 432180 | G | A | upstream_gene_variant | MODIFIER | c.-4347G>A| |
S272 |
2 | BAA05g00760 | A05 | 433197 | G | A | upstream_gene_variant | MODIFIER | c.-3330G>A| |
S25 |
3 | BAA05g00760 | A05 | 433204 | G | A | upstream_gene_variant | MODIFIER | c.-3323G>A| |
S62 |
4 | BAA05g00760 | A05 | 433991 | C | T | upstream_gene_variant | MODIFIER | c.-2536C>T| |
S284 S9 |
5 | BAA05g00760 | A05 | 434320 | C | T | upstream_gene_variant | MODIFIER | c.-2207C>T| |
S59 |
6 | BAA05g00760 | A05 | 434817 | C | T | upstream_gene_variant | MODIFIER | c.-1710C>T| |
S303 |
7 | BAA05g00760 | A05 | 434827 | C | T | upstream_gene_variant | MODIFIER | c.-1700C>T| |
S123 |
8 | BAA05g00760 | A05 | 435301 | C | T | upstream_gene_variant | MODIFIER | c.-1226C>T| |
S25 |
9 | BAA05g00760 | A05 | 436729 | G | A | missense_variant | MODERATE | c.203G>A|p.Gly68Glu |
S277 |
10 | BAA05g00760 | A05 | 437574 | C | T | synonymous_variant | LOW | c.853C>T|p.Leu285Leu |
S276 |
11 | BAA05g00760 | A05 | 437578 | C | T | missense_variant | MODERATE | c.857C>T|p.Ala286Val |
S181 |