Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g18120 | A05 | 10353347 | C | T | downstream_gene_variant | MODIFIER | c.*3022G>A| |
S71 |
2 | BAA05g18120 | A05 | 10353558 | C | G | downstream_gene_variant | MODIFIER | c.*2811G>C| |
S87 |
3 | BAA05g18120 | A05 | 10353619 | C | T | downstream_gene_variant | MODIFIER | c.*2750G>A| |
S87 |
4 | BAA05g18120 | A05 | 10354512 | C | T | downstream_gene_variant | MODIFIER | c.*1857G>A| |
S18 |
5 | BAA05g18120 | A05 | 10355330 | C | T | downstream_gene_variant | MODIFIER | c.*1039G>A| |
S35 |
6 | BAA05g18120 | A05 | 10356286 | G | T | downstream_gene_variant | MODIFIER | c.*83C>A| |
S67 |
7 | BAA05g18120 | A05 | 10358020 | C | T | missense_variant | MODERATE | c.614G>A|p.Gly205Glu |
S175 |
8 | BAA05g18120 | A05 | 10358141 | G | A | missense_variant | MODERATE | c.493C>T|p.Pro165Ser |
S203 |
9 | BAA05g18120 | A05 | 10358837 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.181-1G>A| |
S166 |
10 | BAA05g18120 | A05 | 10362279 | C | T | upstream_gene_variant | MODIFIER | c.-3107G>A| |
S256 |
11 | BAA05g18120 | A05 | 10363007 | G | A | upstream_gene_variant | MODIFIER | c.-3835C>T| |
S161 |