Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g16590 | A04 | 20984488 | G | A | missense_variant | MODERATE | c.35C>T|p.Ala12Val |
S35 |
2 | BAA04g16590 | A04 | 20985188 | G | A | upstream_gene_variant | MODIFIER | c.-666C>T| |
S223 |
3 | BAA04g16590 | A04 | 20985211 | G | A | upstream_gene_variant | MODIFIER | c.-689C>T| |
S287 |
4 | BAA04g16590 | A04 | 20985548 | G | A | upstream_gene_variant | MODIFIER | c.-1026C>T| |
S266 |
5 | BAA04g16590 | A04 | 20987664 | G | A | upstream_gene_variant | MODIFIER | c.-3142C>T| |
S282 |
6 | BAA04g16590 | A04 | 20987686 | G | A | upstream_gene_variant | MODIFIER | c.-3164C>T| |
S130 |
7 | BAA04g16590 | A04 | 20987858 | C | T | upstream_gene_variant | MODIFIER | c.-3336G>A| |
S1 S90 |
8 | BAA04g16590 | A04 | 20988005 | G | A | upstream_gene_variant | MODIFIER | c.-3483C>T| |
S104 S52 |
9 | BAA04g16590 | A04 | 20988454 | C | T | upstream_gene_variant | MODIFIER | c.-3932G>A| |
S138 |
10 | BAA04g16590 | A04 | 20988690 | C | T | upstream_gene_variant | MODIFIER | c.-4168G>A| |
S55 |
11 | BAA04g16590 | A04 | 20988882 | C | T | upstream_gene_variant | MODIFIER | c.-4360G>A| |
S18 |