Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g01770 | A02 | 779962 | C | T | synonymous_variant | LOW | c.2649G>A|p.Arg883Arg |
S183 S198 |
2 | BAA02g01770 | A02 | 780163 | C | T | synonymous_variant | LOW | c.2448G>A|p.Glu816Glu |
S83 S88 |
3 | BAA02g01770 | A02 | 783037 | G | A | missense_variant | MODERATE | c.1910C>T|p.Ser637Phe |
S286 |
4 | BAA02g01770 | A02 | 783408 | G | A | synonymous_variant | LOW | c.1539C>T|p.His513His |
S68 |
5 | BAA02g01770 | A02 | 785526 | C | T | synonymous_variant | LOW | c.1053G>A|p.Glu351Glu |
S61 |
6 | BAA02g01770 | A02 | 785920 | C | T | missense_variant | MODERATE | c.659G>A|p.Arg220Lys |
S207 |
7 | BAA02g01770 | A02 | 786225 | C | T | synonymous_variant | LOW | c.354G>A|p.Leu118Leu |
S262 |
8 | BAA02g01770 | A02 | 786560 | C | T | missense_variant | MODERATE | c.19G>A|p.Asp7Asn |
S262 |
9 | BAA02g01770 | A02 | 788574 | G | A | upstream_gene_variant | MODIFIER | c.-1996C>T| |
S273 |
10 | BAA02g01770 | A02 | 789449 | C | T | upstream_gene_variant | MODIFIER | c.-2871G>A| |
S272 |