Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g04180 | A10 | 2087032 | C | T | missense_variant | MODERATE | c.269G>A|p.Arg90His |
S47 |
2 | BAA10g04180 | A10 | 2087569 | C | T | intron_variant | MODIFIER | c.204-472G>A| |
S79 S91 |
3 | BAA10g04180 | A10 | 2090191 | G | A | upstream_gene_variant | MODIFIER | c.-1578C>T| |
S16 |
4 | BAA10g04180 | A10 | 2091699 | G | A | upstream_gene_variant | MODIFIER | c.-3086C>T| |
S240 |
5 | BAA10g04180 | A10 | 2091864 | C | T | upstream_gene_variant | MODIFIER | c.-3251G>A| |
S204 |
6 | BAA10g04180 | A10 | 2092094 | C | T | upstream_gene_variant | MODIFIER | c.-3481G>A| |
S188 |