Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g14180 | A05 | 7444286 | C | T | upstream_gene_variant | MODIFIER | c.-4419C>T| |
S45 |
2 | BAA05g14180 | A05 | 7445728 | G | A | upstream_gene_variant | MODIFIER | c.-2977G>A| |
S208 |
3 | BAA05g14180 | A05 | 7446140 | G | A | upstream_gene_variant | MODIFIER | c.-2565G>A| |
S225 |
4 | BAA05g14180 | A05 | 7446730 | G | A | upstream_gene_variant | MODIFIER | c.-1975G>A| |
S230 |
5 | BAA05g14180 | A05 | 7447276 | C | T | upstream_gene_variant | MODIFIER | c.-1429C>T| |
S181 |
6 | BAA05g14180 | A05 | 7447474 | G | A | upstream_gene_variant | MODIFIER | c.-1231G>A| |
S66 |
7 | BAA05g14180 | A05 | 7448672 | G | A | upstream_gene_variant | MODIFIER | c.-33G>A| |
S296 |
8 | BAA05g14180 | A05 | 7449219 | C | T | synonymous_variant | LOW | c.430C>T|p.Leu144Leu |
S133 |
9 | BAA05g14180 | A05 | 7449730 | C | T | missense_variant | MODERATE | c.767C>T|p.Thr256Met |
S100 |
10 | BAA05g14180 | A05 | 7449831 | G | A | missense_variant | MODERATE | c.868G>A|p.Asp290Asn |
S221 |
11 | BAA05g14180 | A05 | 7450014 | C | T | synonymous_variant | LOW | c.1051C>T|p.Leu351Leu |
S100 |
12 | BAA05g14180 | A05 | 7450475 | C | T | downstream_gene_variant | MODIFIER | c.*285C>T| |
S133 |
13 | BAA05g14180 | A05 | 7451654 | G | A | downstream_gene_variant | MODIFIER | c.*1464G>A| |
S282 |