Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g45390 | A01 | 30283307 | C | T | downstream_gene_variant | MODIFIER | c.*4603G>A| |
S62 |
2 | BAA01g45390 | A01 | 30284477 | G | A | downstream_gene_variant | MODIFIER | c.*3433C>T| |
S9 |
3 | BAA01g45390 | A01 | 30285003 | G | A | downstream_gene_variant | MODIFIER | c.*2907C>T| |
S181 |
4 | BAA01g45390 | A01 | 30286328 | C | T | downstream_gene_variant | MODIFIER | c.*1582G>A| |
S107 |
5 | BAA01g45390 | A01 | 30286814 | C | T | downstream_gene_variant | MODIFIER | c.*1096G>A| |
S41 |
6 | BAA01g45390 | A01 | 30286996 | C | T | downstream_gene_variant | MODIFIER | c.*914G>A| |
S27 S39 |
7 | BAA01g45390 | A01 | 30287680 | G | A | downstream_gene_variant | MODIFIER | c.*230C>T| |
S138 |
8 | BAA01g45390 | A01 | 30288423 | G | A | synonymous_variant | LOW | c.1656C>T|p.Ile552Ile |
S173 |
9 | BAA01g45390 | A01 | 30288962 | C | T | missense_variant | MODERATE | c.1117G>A|p.Ala373Thr |
S186 |
10 | BAA01g45390 | A01 | 30289575 | G | A | synonymous_variant | LOW | c.504C>T|p.Ile168Ile |
S135 |
11 | BAA01g45390 | A01 | 30289777 | G | A | missense_variant | MODERATE | c.302C>T|p.Thr101Ile |
S238 |
12 | BAA01g45390 | A01 | 30289897 | C | T | missense_variant | MODERATE | c.182G>A|p.Gly61Glu |
S62 |
13 | BAA01g45390 | A01 | 30290024 | C | T | missense_variant | MODERATE | c.55G>A|p.Asp19Asn |
S282 |