Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g44490 | A01 | 29564657 | C | T | missense_variant | MODERATE | c.1169G>A|p.Arg390Lys |
S8 |
2 | BAA01g44490 | A01 | 29565121 | G | A | synonymous_variant | LOW | c.943C>T|p.Leu315Leu |
S280 |
3 | BAA01g44490 | A01 | 29565313 | C | T | synonymous_variant | LOW | c.825G>A|p.Gln275Gln |
S72 S78 |
4 | BAA01g44490 | A01 | 29566095 | G | A | synonymous_variant | LOW | c.210C>T|p.Phe70Phe |
S287 |
5 | BAA01g44490 | A01 | 29567818 | C | T | upstream_gene_variant | MODIFIER | c.-654G>A| |
S73 S91 |
6 | BAA01g44490 | A01 | 29567931 | G | A | upstream_gene_variant | MODIFIER | c.-767C>T| |
S129 |
7 | BAA01g44490 | A01 | 29568202 | G | A | upstream_gene_variant | MODIFIER | c.-1038C>T| |
S38 |
8 | BAA01g44490 | A01 | 29568282 | A | G | upstream_gene_variant | MODIFIER | c.-1118T>C| |
S252 S293 S294 S36 |
9 | BAA01g44490 | A01 | 29568356 | G | A | upstream_gene_variant | MODIFIER | c.-1192C>T| |
S105 S106 |
10 | BAA01g44490 | A01 | 29569065 | C | T | upstream_gene_variant | MODIFIER | c.-1901G>A| |
S288 |