Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g42670 | A05 | 40331590 | C | T | missense_variant | MODERATE | c.112G>A|p.Asp38Asn |
S77 |
2 | BAA05g42670 | A05 | 40331674 | G | A | synonymous_variant | LOW | c.28C>T|p.Leu10Leu |
S148 S210 |
3 | BAA05g42670 | A05 | 40332820 | C | T | upstream_gene_variant | MODIFIER | c.-1119G>A| |
S221 |
4 | BAA05g42670 | A05 | 40335107 | G | A | upstream_gene_variant | MODIFIER | c.-3406C>T| |
S255 |
5 | BAA05g42670 | A05 | 40335148 | G | A | upstream_gene_variant | MODIFIER | c.-3447C>T| |
S10 |
6 | BAA05g42670 | A05 | 40335390 | C | T | upstream_gene_variant | MODIFIER | c.-3689G>A| |
S123 |
7 | BAA05g42670 | A05 | 40336114 | G | A | upstream_gene_variant | MODIFIER | c.-4413C>T| |
S308 |