Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g18030 | A03 | 7945805 | C | T | missense_variant | MODERATE | c.2270G>A|p.Gly757Glu |
S216 |
2 | BAA03g18030 | A03 | 7945880 | G | A | missense_variant | MODERATE | c.2195C>T|p.Ser732Phe |
S39 |
3 | BAA03g18030 | A03 | 7946147 | G | A | missense_variant | MODERATE | c.2068C>T|p.Leu690Phe |
S296 |
4 | BAA03g18030 | A03 | 7946210 | C | T | missense_variant | MODERATE | c.2005G>A|p.Ala669Thr |
S250 |
5 | BAA03g18030 | A03 | 7947628 | G | A | stop_gained | HIGH | c.772C>T|p.Gln258* |
S67 |
6 | BAA03g18030 | A03 | 7948148 | C | T | synonymous_variant | LOW | c.252G>A|p.Lys84Lys |
S73 S91 |
7 | BAA03g18030 | A03 | 7952063 | G | A | upstream_gene_variant | MODIFIER | c.-3523C>T| |
S140 S168 S219 S279 S64 S72 |
8 | BAA03g18030 | A03 | 7952304 | C | T | upstream_gene_variant | MODIFIER | c.-3764G>A| |
S112 |
9 | BAA03g18030 | A03 | 7952695 | G | A | upstream_gene_variant | MODIFIER | c.-4155C>T| |
S169 |