Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g17670 | A05 | 9977292 | G | A | upstream_gene_variant | MODIFIER | c.-1632G>A| |
S168 |
2 | BAA05g17670 | A05 | 9977309 | C | T | upstream_gene_variant | MODIFIER | c.-1615C>T| |
S186 |
3 | BAA05g17670 | A05 | 9977319 | C | T | upstream_gene_variant | MODIFIER | c.-1605C>T| |
S113 |
4 | BAA05g17670 | A05 | 9978045 | C | T | upstream_gene_variant | MODIFIER | c.-879C>T| |
S118 |
5 | BAA05g17670 | A05 | 9978427 | C | T | upstream_gene_variant | MODIFIER | c.-497C>T| |
S153 S213 |
6 | BAA05g17670 | A05 | 9978480 | C | T | upstream_gene_variant | MODIFIER | c.-444C>T| |
S33 |
7 | BAA05g17670 | A05 | 9978580 | C | T | upstream_gene_variant | MODIFIER | c.-344C>T| |
S13 |
8 | BAA05g17670 | A05 | 9979017 | C | T | missense_variant | MODERATE | c.94C>T|p.Pro32Ser |
S71 |
9 | BAA05g17670 | A05 | 9979363 | G | A | missense_variant | MODERATE | c.440G>A|p.Gly147Glu |
S185 |
10 | BAA05g17670 | A05 | 9980947 | C | T | missense_variant | MODERATE | c.1943C>T|p.Pro648Leu |
S262 |