Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g10620 | A05 | 5393585 | G | A | upstream_gene_variant | MODIFIER | c.-3602G>A| |
S122 |
2 | BAA05g10620 | A05 | 5393966 | C | T | upstream_gene_variant | MODIFIER | c.-3221C>T| |
S119 |
3 | BAA05g10620 | A05 | 5394166 | C | T | upstream_gene_variant | MODIFIER | c.-3021C>T| |
S72 S78 |
4 | BAA05g10620 | A05 | 5395584 | C | T | upstream_gene_variant | MODIFIER | c.-1603C>T| |
S218 |
5 | BAA05g10620 | A05 | 5395851 | G | A | upstream_gene_variant | MODIFIER | c.-1336G>A| |
S190 |
6 | BAA05g10620 | A05 | 5396934 | A | C | upstream_gene_variant | MODIFIER | c.-253A>C| |
S28 |
7 | BAA05g10620 | A05 | 5397305 | C | T | missense_variant | MODERATE | c.119C>T|p.Ser40Phe |
S250 |
8 | BAA05g10620 | A05 | 5398289 | C | T | missense_variant | MODERATE | c.515C>T|p.Ser172Phe |
S303 |
9 | BAA05g10620 | A05 | 5399115 | C | T | missense_variant | MODERATE | c.1016C>T|p.Ser339Phe |
S278 |
10 | BAA05g10620 | A05 | 5399301 | G | A | missense_variant | MODERATE | c.1202G>A|p.Gly401Glu |
S158 |
11 | BAA05g10620 | A05 | 5402652 | C | T | downstream_gene_variant | MODIFIER | c.*2890C>T| |
S295 |
12 | BAA05g10620 | A05 | 5402775 | G | A | downstream_gene_variant | MODIFIER | c.*3013G>A| |
S120 |