Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g01830 | A09 | 1267123 | C | T | missense_variant | MODERATE | c.1543G>A|p.Gly515Ser |
S303 |
2 | BAA09g01830 | A09 | 1267333 | C | T | missense_variant | MODERATE | c.1333G>A|p.Asp445Asn |
S278 |
3 | BAA09g01830 | A09 | 1269480 | G | A | synonymous_variant | LOW | c.60C>T|p.Thr20Thr |
S113 |
4 | BAA09g01830 | A09 | 1270397 | G | A | upstream_gene_variant | MODIFIER | c.-858C>T| |
S246 |
5 | BAA09g01830 | A09 | 1270597 | G | A | upstream_gene_variant | MODIFIER | c.-1058C>T| |
S302 |
6 | BAA09g01830 | A09 | 1270792 | G | A | upstream_gene_variant | MODIFIER | c.-1253C>T| |
S271 |
7 | BAA09g01830 | A09 | 1273078 | G | A | upstream_gene_variant | MODIFIER | c.-3539C>T| |
S139 |