Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g09430 | A01 | 4194263 | G | A | missense_variant | MODERATE | c.3955C>T|p.Pro1319Ser |
S37 |
2 | BAA01g09430 | A01 | 4194503 | G | A | missense_variant | MODERATE | c.3803C>T|p.Ser1268Phe |
S190 |
3 | BAA01g09430 | A01 | 4194997 | C | T | missense_variant | MODERATE | c.3484G>A|p.Ala1162Thr |
S128 |
4 | BAA01g09430 | A01 | 4196684 | G | A | missense_variant | MODERATE | c.2195C>T|p.Ser732Phe |
S5 |
5 | BAA01g09430 | A01 | 4197985 | C | T | missense_variant | MODERATE | c.1306G>A|p.Glu436Lys |
S130 |
6 | BAA01g09430 | A01 | 4199552 | C | T | synonymous_variant | LOW | c.78G>A|p.Gly26Gly |
S263 |
7 | BAA01g09430 | A01 | 4201703 | G | A | upstream_gene_variant | MODIFIER | c.-2074C>T| |
S157 S163 |
8 | BAA01g09430 | A01 | 4202423 | G | A | upstream_gene_variant | MODIFIER | c.-2794C>T| |
S32 |
9 | BAA01g09430 | A01 | 4203601 | C | T | upstream_gene_variant | MODIFIER | c.-3972G>A| |
S20 |
10 | BAA01g09430 | A01 | 4203787 | C | T | upstream_gene_variant | MODIFIER | c.-4158G>A| |
S206 S26 |