Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g42630 | A02 | 35468478 | G | A | upstream_gene_variant | MODIFIER | c.-3016G>A| |
S142 |
2 | BAA02g42630 | A02 | 35470012 | G | A | upstream_gene_variant | MODIFIER | c.-1482G>A| |
S286 |
3 | BAA02g42630 | A02 | 35470177 | C | T | upstream_gene_variant | MODIFIER | c.-1317C>T| |
S239 |
4 | BAA02g42630 | A02 | 35470391 | G | A | upstream_gene_variant | MODIFIER | c.-1103G>A| |
S207 |
5 | BAA02g42630 | A02 | 35470603 | G | A | upstream_gene_variant | MODIFIER | c.-891G>A| |
S265 |
6 | BAA02g42630 | A02 | 35471983 | G | A | missense_variant | MODERATE | c.490G>A|p.Asp164Asn |
S280 |
7 | BAA02g42630 | A02 | 35472219 | G | A | synonymous_variant | LOW | c.726G>A|p.Lys242Lys |
S288 |
8 | BAA02g42630 | A02 | 35473016 | G | A | missense_variant | MODERATE | c.1523G>A|p.Arg508Lys |
S20 |
9 | BAA02g42630 | A02 | 35473500 | G | A | synonymous_variant | LOW | c.2007G>A|p.Gln669Gln |
S125 |
10 | BAA02g42630 | A02 | 35474045 | C | T | missense_variant | MODERATE | c.2552C>T|p.Thr851Ile |
S197 |
11 | BAA02g42630 | A02 | 35474150 | G | A | missense_variant | MODERATE | c.2657G>A|p.Ser886Asn |
S23 |