Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g18420 | A02 | 9403694 | C | T | synonymous_variant | LOW | c.1518G>A|p.Arg506Arg |
S224 |
2 | BAA02g18420 | A02 | 9404086 | C | T | missense_variant | MODERATE | c.1126G>A|p.Asp376Asn |
S245 |
3 | BAA02g18420 | A02 | 9404231 | G | A | synonymous_variant | LOW | c.981C>T|p.Phe327Phe |
S47 S48 |
4 | BAA02g18420 | A02 | 9404277 | C | T | missense_variant | MODERATE | c.935G>A|p.Ser312Asn |
S135 |
5 | BAA02g18420 | A02 | 9405238 | C | T | synonymous_variant | LOW | c.789G>A|p.Lys263Lys |
S119 |
6 | BAA02g18420 | A02 | 9408795 | G | A | upstream_gene_variant | MODIFIER | c.-2769C>T| |
S20 |
7 | BAA02g18420 | A02 | 9409442 | C | T | upstream_gene_variant | MODIFIER | c.-3416G>A| |
S186 |
8 | BAA02g18420 | A02 | 9409531 | C | T | upstream_gene_variant | MODIFIER | c.-3505G>A| |
S178 |
9 | BAA02g18420 | A02 | 9409854 | G | A | upstream_gene_variant | MODIFIER | c.-3828C>T| |
S150 |
10 | BAA02g18420 | A02 | 9410102 | C | T | upstream_gene_variant | MODIFIER | c.-4076G>A| |
S71 |