Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g08550 | A05 | 4260798 | C | T | upstream_gene_variant | MODIFIER | c.-2830C>T| |
S216 |
2 | BAA05g08550 | A05 | 4261527 | C | T | upstream_gene_variant | MODIFIER | c.-2101C>T| |
S110 |
3 | BAA05g08550 | A05 | 4261741 | G | A | upstream_gene_variant | MODIFIER | c.-1887G>A| |
S40 S49 |
4 | BAA05g08550 | A05 | 4262632 | G | A | upstream_gene_variant | MODIFIER | c.-996G>A| |
S268 |
5 | BAA05g08550 | A05 | 4262698 | G | A | upstream_gene_variant | MODIFIER | c.-930G>A| |
S284 |
6 | BAA05g08550 | A05 | 4263313 | C | T | upstream_gene_variant | MODIFIER | c.-315C>T| |
S99 |
7 | BAA05g08550 | A05 | 4263619 | C | T | upstream_gene_variant | MODIFIER | c.-9C>T| |
S89 |
8 | BAA05g08550 | A05 | 4264640 | G | A | missense_variant | MODERATE | c.395G>A|p.Gly132Glu |
S240 |
9 | BAA05g08550 | A05 | 4264682 | C | T | missense_variant | MODERATE | c.437C>T|p.Pro146Leu |
S61 |
10 | BAA05g08550 | A05 | 4264686 | G | A | synonymous_variant | LOW | c.441G>A|p.Leu147Leu |
S55 |
11 | BAA05g08550 | A05 | 4264736 | C | T | missense_variant | MODERATE | c.491C>T|p.Ala164Val |
S163 |
12 | BAA05g08550 | A05 | 4264916 | G | A | synonymous_variant | LOW | c.585G>A|p.Lys195Lys |
S86 |