Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g59660 | A03 | 29948194 | G | A | upstream_gene_variant | MODIFIER | c.-3423G>A| |
S233 |
2 | BAA03g59660 | A03 | 29949208 | G | A | upstream_gene_variant | MODIFIER | c.-2409G>A| |
S205 |
3 | BAA03g59660 | A03 | 29949257 | C | T | upstream_gene_variant | MODIFIER | c.-2360C>T| |
S211 |
4 | BAA03g59660 | A03 | 29949685 | G | A | upstream_gene_variant | MODIFIER | c.-1932G>A| |
S202 |
5 | BAA03g59660 | A03 | 29949848 | G | A | upstream_gene_variant | MODIFIER | c.-1769G>A| |
S7 |
6 | BAA03g59660 | A03 | 29951285 | C | T | upstream_gene_variant | MODIFIER | c.-332C>T| |
S78 S83 |
7 | BAA03g59660 | A03 | 29951756 | C | T | missense_variant | MODERATE | c.140C>T|p.Ser47Phe |
S57 |
8 | BAA03g59660 | A03 | 29952322 | C | T | missense_variant | MODERATE | c.376C>T|p.Pro126Ser |
S71 |
9 | BAA03g59660 | A03 | 29952616 | A | T | missense_variant | MODERATE | c.670A>T|p.Thr224Ser |
S269 |
10 | BAA03g59660 | A03 | 29955265 | C | T | downstream_gene_variant | MODIFIER | c.*2377C>T| |
S158 |
11 | BAA03g59660 | A03 | 29956095 | G | A | downstream_gene_variant | MODIFIER | c.*3207G>A| |
S150 |
12 | BAA03g59660 | A03 | 29957790 | C | T | downstream_gene_variant | MODIFIER | c.*4902C>T| |
S184 |