Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g47970 | A09 | 51992977 | G | A | upstream_gene_variant | MODIFIER | c.-3552G>A| |
S13 |
2 | BAA09g47970 | A09 | 51997059 | G | A | missense_variant | MODERATE | c.281G>A|p.Cys94Tyr |
S288 |
3 | BAA09g47970 | A09 | 51997135 | G | A | splice_region_variant&intron_variant | LOW | c.285-8G>A| |
S150 |
4 | BAA09g47970 | A09 | 51999033 | C | T | downstream_gene_variant | MODIFIER | c.*1504C>T| |
S140 |
5 | BAA09g47970 | A09 | 51999130 | C | A | downstream_gene_variant | MODIFIER | c.*1601C>A| |
S144 |
6 | BAA09g47970 | A09 | 51999238 | G | A | downstream_gene_variant | MODIFIER | c.*1709G>A| |
S202 |
7 | BAA09g47970 | A09 | 52002113 | C | T | downstream_gene_variant | MODIFIER | c.*4584C>T| |
S92 |