Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g42640 | A02 | 35475532 | C | T | upstream_gene_variant | MODIFIER | c.-2725C>T| |
S178 |
2 | BAA02g42640 | A02 | 35476483 | G | A | upstream_gene_variant | MODIFIER | c.-1774G>A| |
S84 S93 |
3 | BAA02g42640 | A02 | 35478453 | G | A | missense_variant | MODERATE | c.197G>A|p.Arg66Lys |
S225 |
4 | BAA02g42640 | A02 | 35478761 | G | A | missense_variant | MODERATE | c.505G>A|p.Asp169Asn |
S37 |
5 | BAA02g42640 | A02 | 35478767 | G | A | missense_variant | MODERATE | c.511G>A|p.Glu171Lys |
S199 |
6 | BAA02g42640 | A02 | 35479339 | G | A | synonymous_variant | LOW | c.1083G>A|p.Lys361Lys |
S25 |
7 | BAA02g42640 | A02 | 35479808 | G | A | missense_variant | MODERATE | c.1552G>A|p.Asp518Asn |
S19 |
8 | BAA02g42640 | A02 | 35480153 | C | T | missense_variant | MODERATE | c.1897C>T|p.Pro633Ser |
S63 |
9 | BAA02g42640 | A02 | 35481097 | C | T | downstream_gene_variant | MODIFIER | c.*318C>T| |
S270 |
10 | BAA02g42640 | A02 | 35484478 | A | G | downstream_gene_variant | MODIFIER | c.*3699A>G| |
S168 |
11 | BAA02g42640 | A02 | 35485016 | A | G | downstream_gene_variant | MODIFIER | c.*4237A>G| |
S245 |