Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g19830 | A02 | 10392763 | C | T | synonymous_variant | LOW | c.2487G>A|p.Lys829Lys |
S2 |
2 | BAA02g19830 | A02 | 10392781 | G | A | synonymous_variant | LOW | c.2469C>T|p.Val823Val |
S209 |
3 | BAA02g19830 | A02 | 10393053 | C | T | missense_variant | MODERATE | c.2197G>A|p.Ala733Thr |
S165 |
4 | BAA02g19830 | A02 | 10393428 | C | T | missense_variant | MODERATE | c.1822G>A|p.Glu608Lys |
S302 |
5 | BAA02g19830 | A02 | 10393660 | G | A | synonymous_variant | LOW | c.1590C>T|p.Phe530Phe |
S5 |
6 | BAA02g19830 | A02 | 10394549 | C | T | intron_variant | MODIFIER | c.899-198G>A| |
S273 |
7 | BAA02g19830 | A02 | 10396088 | C | T | missense_variant | MODERATE | c.157G>A|p.Val53Ile |
S104 S52 |
8 | BAA02g19830 | A02 | 10397514 | G | A | upstream_gene_variant | MODIFIER | c.-1270C>T| |
S229 |
9 | BAA02g19830 | A02 | 10398190 | G | A | upstream_gene_variant | MODIFIER | c.-1946C>T| |
S149 |
10 | BAA02g19830 | A02 | 10399332 | G | A | upstream_gene_variant | MODIFIER | c.-3088C>T| |
S91 |
11 | BAA02g19830 | A02 | 10400345 | G | A | upstream_gene_variant | MODIFIER | c.-4101C>T| |
S306 S308 |
12 | BAA02g19830 | A02 | 10400601 | G | A | upstream_gene_variant | MODIFIER | c.-4357C>T| |
S190 |