Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g43310 | A02 | 35915971 | C | T | upstream_gene_variant | MODIFIER | c.-4186C>T| |
S277 |
2 | BAA02g43310 | A02 | 35916331 | G | A | upstream_gene_variant | MODIFIER | c.-3826G>A| |
S55 |
3 | BAA02g43310 | A02 | 35920612 | G | A | missense_variant | MODERATE | c.376G>A|p.Glu126Lys |
S211 S227 |
4 | BAA02g43310 | A02 | 35921515 | G | A | synonymous_variant | LOW | c.840G>A|p.Gln280Gln |
S143 |
5 | BAA02g43310 | A02 | 35922033 | C | T | synonymous_variant | LOW | c.1113C>T|p.Leu371Leu |
S267 |
6 | BAA02g43310 | A02 | 35922426 | C | T | missense_variant | MODERATE | c.1348C>T|p.Leu450Phe |
S256 |
7 | BAA02g43310 | A02 | 35922448 | G | A | missense_variant | MODERATE | c.1370G>A|p.Ser457Asn |
S232 |
8 | BAA02g43310 | A02 | 35922871 | G | A | missense_variant | MODERATE | c.1630G>A|p.Asp544Asn |
S11 |
9 | BAA02g43310 | A02 | 35923555 | C | T | synonymous_variant | LOW | c.1984C>T|p.Leu662Leu |
S173 |
10 | BAA02g43310 | A02 | 35924284 | G | A | missense_variant | MODERATE | c.2299G>A|p.Val767Ile |
S148 S31 |
11 | BAA02g43310 | A02 | 35924663 | C | T | missense_variant | MODERATE | c.2522C>T|p.Ala841Val |
S115 |
12 | BAA02g43310 | A02 | 35925790 | G | A | missense_variant | MODERATE | c.3143G>A|p.Gly1048Asp |
S139 |
13 | BAA02g43310 | A02 | 35925977 | C | T | synonymous_variant | LOW | c.3330C>T|p.Asp1110Asp |
S263 |
14 | BAA02g43310 | A02 | 35929175 | C | T | downstream_gene_variant | MODIFIER | c.*3054C>T| |
S118 |