Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g03200 | A01 | 1443448 | G | A | missense_variant | MODERATE | c.1046C>T|p.Ala349Val |
S293 |
2 | BAA01g03200 | A01 | 1443750 | C | T | missense_variant | MODERATE | c.814G>A|p.Ala272Thr |
S47 |
3 | BAA01g03200 | A01 | 1445170 | G | A | intron_variant | MODIFIER | c.183+44C>T| |
S175 |
4 | BAA01g03200 | A01 | 1445193 | G | A | intron_variant | MODIFIER | c.183+21C>T| |
S135 S152 S185 S203 S273 |
5 | BAA01g03200 | A01 | 1445917 | G | A | upstream_gene_variant | MODIFIER | c.-521C>T| |
S65 |
6 | BAA01g03200 | A01 | 1446825 | G | A | upstream_gene_variant | MODIFIER | c.-1429C>T| |
S295 |
7 | BAA01g03200 | A01 | 1446899 | G | A | upstream_gene_variant | MODIFIER | c.-1503C>T| |
S239 |
8 | BAA01g03200 | A01 | 1448650 | G | A | upstream_gene_variant | MODIFIER | c.-3254C>T| |
S263 |
9 | BAA01g03200 | A01 | 1449545 | G | A | upstream_gene_variant | MODIFIER | c.-4149C>T| |
S302 |
10 | BAA01g03200 | A01 | 1449821 | C | T | upstream_gene_variant | MODIFIER | c.-4425G>A| |
S266 S297 S55 S65 |