Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g15370 | A02 | 7382486 | C | T | synonymous_variant | LOW | c.2589G>A|p.Lys863Lys |
S182 |
2 | BAA02g15370 | A02 | 7383205 | G | A | missense_variant | MODERATE | c.1870C>T|p.Pro624Ser |
S191 |
3 | BAA02g15370 | A02 | 7383403 | C | T | missense_variant | MODERATE | c.1672G>A|p.Asp558Asn |
S209 |
4 | BAA02g15370 | A02 | 7383751 | A | C | missense_variant | MODERATE | c.1324T>G|p.Phe442Val |
S100 S123 S128 S208 S211 S230 S249 S250 S265 S297 S39 S67 S69 S74 S87 |
5 | BAA02g15370 | A02 | 7384124 | G | A | synonymous_variant | LOW | c.951C>T|p.Asn317Asn |
S263 |
6 | BAA02g15370 | A02 | 7385125 | G | A | upstream_gene_variant | MODIFIER | c.-51C>T| |
S33 |
7 | BAA02g15370 | A02 | 7385134 | G | A | upstream_gene_variant | MODIFIER | c.-60C>T| |
S188 |
8 | BAA02g15370 | A02 | 7386945 | C | T | upstream_gene_variant | MODIFIER | c.-1871G>A| |
S210 |
9 | BAA02g15370 | A02 | 7389864 | G | A | upstream_gene_variant | MODIFIER | c.-4790C>T| |
S177 |