Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g66860 | A03 | 41397803 | C | T | upstream_gene_variant | MODIFIER | c.-4396C>T| |
S251 |
2 | BAA03g66860 | A03 | 41399169 | C | T | upstream_gene_variant | MODIFIER | c.-3030C>T| |
S105 S106 |
3 | BAA03g66860 | A03 | 41399614 | C | T | upstream_gene_variant | MODIFIER | c.-2585C>T| |
S238 |
4 | BAA03g66860 | A03 | 41401416 | G | A | upstream_gene_variant | MODIFIER | c.-783G>A| |
S295 |
5 | BAA03g66860 | A03 | 41401419 | C | T | upstream_gene_variant | MODIFIER | c.-780C>T| |
S33 |
6 | BAA03g66860 | A03 | 41402571 | C | T | missense_variant | MODERATE | c.113C>T|p.Thr38Ile |
S78 S83 |
7 | BAA03g66860 | A03 | 41402619 | C | T | missense_variant | MODERATE | c.161C>T|p.Thr54Ile |
S144 |
8 | BAA03g66860 | A03 | 41403014 | G | A | synonymous_variant | LOW | c.465G>A|p.Lys155Lys |
S242 |
9 | BAA03g66860 | A03 | 41403105 | G | A | missense_variant | MODERATE | c.556G>A|p.Val186Ile |
S69 |
10 | BAA03g66860 | A03 | 41403351 | G | A | missense_variant | MODERATE | c.802G>A|p.Ala268Thr |
S177 |
11 | BAA03g66860 | A03 | 41403489 | G | A | missense_variant | MODERATE | c.940G>A|p.Gly314Arg |
S48 |