Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g45450 | A02 | 37206000 | C | T | downstream_gene_variant | MODIFIER | c.*1797G>A| |
S171 |
2 | BAA02g45450 | A02 | 37206646 | C | T | downstream_gene_variant | MODIFIER | c.*1151G>A| |
S74 |
3 | BAA02g45450 | A02 | 37207997 | G | A | missense_variant | MODERATE | c.3574C>T|p.Leu1192Phe |
S28 |
4 | BAA02g45450 | A02 | 37208163 | G | A | synonymous_variant | LOW | c.3489C>T|p.Asn1163Asn |
S35 |
5 | BAA02g45450 | A02 | 37208263 | T | A | missense_variant | MODERATE | c.3389A>T|p.Glu1130Val |
S239 |
6 | BAA02g45450 | A02 | 37208743 | C | T | missense_variant | MODERATE | c.3085G>A|p.Glu1029Lys |
S133 |
7 | BAA02g45450 | A02 | 37209438 | C | T | missense_variant | MODERATE | c.2656G>A|p.Glu886Lys |
S189 |
8 | BAA02g45450 | A02 | 37210888 | G | A | missense_variant | MODERATE | c.2012C>T|p.Ser671Phe |
S213 |
9 | BAA02g45450 | A02 | 37212682 | G | A | missense_variant | MODERATE | c.292C>T|p.Leu98Phe |
S286 |
10 | BAA02g45450 | A02 | 37212943 | C | T | missense_variant | MODERATE | c.31G>A|p.Glu11Lys |
S182 |
11 | BAA02g45450 | A02 | 37213544 | C | T | upstream_gene_variant | MODIFIER | c.-571G>A| |
S193 |
12 | BAA02g45450 | A02 | 37213895 | G | A | upstream_gene_variant | MODIFIER | c.-922C>T| |
S246 |
13 | BAA02g45450 | A02 | 37217422 | C | T | upstream_gene_variant | MODIFIER | c.-4449G>A| |
S6 |
14 | BAA02g45450 | A02 | 37217461 | C | T | upstream_gene_variant | MODIFIER | c.-4488G>A| |
S237 |