Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g11640 | A01 | 5387906 | C | T | upstream_gene_variant | MODIFIER | c.-4717C>T| |
S70 |
2 | BAA01g11640 | A01 | 5389994 | C | T | upstream_gene_variant | MODIFIER | c.-2629C>T| |
S164 |
3 | BAA01g11640 | A01 | 5392725 | C | A | missense_variant | MODERATE | c.103C>A|p.Pro35Thr |
S249 |
4 | BAA01g11640 | A01 | 5392799 | C | T | synonymous_variant | LOW | c.177C>T|p.Val59Val |
S53 |
5 | BAA01g11640 | A01 | 5392825 | C | T | splice_region_variant&intron_variant | LOW | c.200+3C>T| |
S296 |
6 | BAA01g11640 | A01 | 5392865 | G | T | intron_variant | MODIFIER | c.201-38G>T| |
S298 |
7 | BAA01g11640 | A01 | 5393551 | C | T | synonymous_variant | LOW | c.693C>T|p.Ile231Ile |
S158 |
8 | BAA01g11640 | A01 | 5393677 | C | T | synonymous_variant | LOW | c.819C>T|p.Ile273Ile |
S58 |
9 | BAA01g11640 | A01 | 5394352 | C | T | missense_variant | MODERATE | c.1199C>T|p.Thr400Ile |
S184 |
10 | BAA01g11640 | A01 | 5395662 | C | T | downstream_gene_variant | MODIFIER | c.*1016C>T| |
S148 S30 S31 |
11 | BAA01g11640 | A01 | 5396022 | C | T | downstream_gene_variant | MODIFIER | c.*1376C>T| |
S130 |
12 | BAA01g11640 | A01 | 5396248 | C | T | downstream_gene_variant | MODIFIER | c.*1602C>T| |
S192 |
13 | BAA01g11640 | A01 | 5398255 | C | T | downstream_gene_variant | MODIFIER | c.*3609C>T| |
S98 |
14 | BAA01g11640 | A01 | 5398908 | G | A | downstream_gene_variant | MODIFIER | c.*4262G>A| |
S15 |