Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g22940 | A03 | 10464485 | G | A | upstream_gene_variant | MODIFIER | c.-3528G>A| |
S188 |
2 | BAA03g22940 | A03 | 10466459 | C | T | upstream_gene_variant | MODIFIER | c.-1554C>T| |
S205 |
3 | BAA03g22940 | A03 | 10466517 | C | T | upstream_gene_variant | MODIFIER | c.-1496C>T| |
S275 |
4 | BAA03g22940 | A03 | 10466772 | G | A | upstream_gene_variant | MODIFIER | c.-1241G>A| |
S210 |
5 | BAA03g22940 | A03 | 10467420 | C | T | upstream_gene_variant | MODIFIER | c.-593C>T| |
S1 S90 |
6 | BAA03g22940 | A03 | 10467844 | C | T | upstream_gene_variant | MODIFIER | c.-169C>T| |
S176 |
7 | BAA03g22940 | A03 | 10468474 | G | A | synonymous_variant | LOW | c.312G>A|p.Arg104Arg |
S152 |
8 | BAA03g22940 | A03 | 10468603 | G | A | synonymous_variant | LOW | c.441G>A|p.Pro147Pro |
S256 |
9 | BAA03g22940 | A03 | 10468647 | G | A | missense_variant | MODERATE | c.485G>A|p.Ser162Asn |
S298 |
10 | BAA03g22940 | A03 | 10468831 | G | A | downstream_gene_variant | MODIFIER | c.*93G>A| |
S64 |
11 | BAA03g22940 | A03 | 10469615 | C | T | downstream_gene_variant | MODIFIER | c.*877C>T| |
S301 |
12 | BAA03g22940 | A03 | 10471392 | C | A | downstream_gene_variant | MODIFIER | c.*2654C>A| |
S237 |