Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g06990 | A04 | 4681273 | G | A | upstream_gene_variant | MODIFIER | c.-1928G>A| |
S277 |
2 | BAA04g06990 | A04 | 4681936 | G | A | upstream_gene_variant | MODIFIER | c.-1265G>A| |
S257 |
3 | BAA04g06990 | A04 | 4683009 | C | T | upstream_gene_variant | MODIFIER | c.-192C>T| |
S272 |
4 | BAA04g06990 | A04 | 4683069 | C | T | upstream_gene_variant | MODIFIER | c.-132C>T| |
S159 S299 |
5 | BAA04g06990 | A04 | 4683453 | G | A | missense_variant | MODERATE | c.253G>A|p.Ala85Thr |
S11 |
6 | BAA04g06990 | A04 | 4684197 | G | A | intron_variant | MODIFIER | c.555+119G>A| |
S261 S30 |
7 | BAA04g06990 | A04 | 4684269 | C | T | intron_variant | MODIFIER | c.555+191C>T| |
S74 |
8 | BAA04g06990 | A04 | 4684504 | C | T | intron_variant | MODIFIER | c.555+426C>T| |
S32 |
9 | BAA04g06990 | A04 | 4686905 | C | T | missense_variant&splice_region_variant | MODERATE | c.710C>T|p.Thr237Met |
S293 |
10 | BAA04g06990 | A04 | 4687089 | C | T | missense_variant | MODERATE | c.808C>T|p.Pro270Ser |
S47 |