Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g09110 | A01 | 3991535 | G | A | missense_variant | MODERATE | c.76C>T|p.Leu26Phe |
S220 S257 S267 S91 |
2 | BAA01g09110 | A01 | 3991546 | G | T | missense_variant | MODERATE | c.65C>A|p.Ser22Tyr |
S220 S257 S267 S91 |
3 | BAA01g09110 | A01 | 3991547 | A | G | missense_variant | MODERATE | c.64T>C|p.Ser22Pro |
S220 S257 S267 S91 |
4 | BAA01g09110 | A01 | 3991566 | C | G | synonymous_variant | LOW | c.45G>C|p.Val15Val |
S220 S257 S267 S91 |
5 | BAA01g09110 | A01 | 3991569 | A | C | missense_variant | MODERATE | c.42T>G|p.Asp14Glu |
S220 S257 S267 S91 |
6 | BAA01g09110 | A01 | 3993559 | C | T | upstream_gene_variant | MODIFIER | c.-1949G>A| |
S54 |
7 | BAA01g09110 | A01 | 3993779 | A | G | upstream_gene_variant | MODIFIER | c.-2169T>C| |
S4 |
8 | BAA01g09110 | A01 | 3994176 | C | T | upstream_gene_variant | MODIFIER | c.-2566G>A| |
S140 |
9 | BAA01g09110 | A01 | 3994417 | C | T | upstream_gene_variant | MODIFIER | c.-2807G>A| |
S50 |
10 | BAA01g09110 | A01 | 3994843 | C | T | upstream_gene_variant | MODIFIER | c.-3233G>A| |
S117 |
11 | BAA01g09110 | A01 | 3995397 | A | C | upstream_gene_variant | MODIFIER | c.-3787T>G| |
S233 |
12 | BAA01g09110 | A01 | 3996145 | C | T | upstream_gene_variant | MODIFIER | c.-4535G>A| |
S303 |