Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g04400 | A01 | 1963754 | C | T | missense_variant | MODERATE | c.1219G>A|p.Val407Met |
S64 |
2 | BAA01g04400 | A01 | 1964047 | G | A | missense_variant | MODERATE | c.1030C>T|p.His344Tyr |
S153 |
3 | BAA01g04400 | A01 | 1964434 | C | T | synonymous_variant | LOW | c.816G>A|p.Val272Val |
S261 |
4 | BAA01g04400 | A01 | 1964629 | G | A | splice_region_variant&intron_variant | LOW | c.804+6C>T| |
S33 |
5 | BAA01g04400 | A01 | 1964709 | C | T | missense_variant | MODERATE | c.730G>A|p.Ala244Thr |
S35 |
6 | BAA01g04400 | A01 | 1969063 | G | A | upstream_gene_variant | MODIFIER | c.-2220C>T| |
S116 |
7 | BAA01g04400 | A01 | 1970031 | C | T | upstream_gene_variant | MODIFIER | c.-3188G>A| |
S36 |
8 | BAA01g04400 | A01 | 1970339 | C | T | upstream_gene_variant | MODIFIER | c.-3496G>A| |
S18 |
9 | BAA01g04400 | A01 | 1970830 | G | A | upstream_gene_variant | MODIFIER | c.-3987C>T| |
S262 |