Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g09940 | A01 | 4445145 | C | T | missense_variant | MODERATE | c.811G>A|p.Gly271Ser |
S38 |
2 | BAA01g09940 | A01 | 4445292 | C | T | missense_variant | MODERATE | c.664G>A|p.Asp222Asn |
S150 |
3 | BAA01g09940 | A01 | 4445415 | C | T | missense_variant | MODERATE | c.541G>A|p.Asp181Asn |
S42 |
4 | BAA01g09940 | A01 | 4445578 | C | T | synonymous_variant | LOW | c.378G>A|p.Lys126Lys |
S92 |
5 | BAA01g09940 | A01 | 4450314 | C | T | upstream_gene_variant | MODIFIER | c.-4037G>A| |
S242 |
6 | BAA01g09940 | A01 | 4450606 | G | T | upstream_gene_variant | MODIFIER | c.-4329C>A| |
S104 S111 S123 S139 S148 S163 S204 S208 S234 S25 S42 S75 S97 |
7 | BAA01g09940 | A01 | 4450652 | C | T | upstream_gene_variant | MODIFIER | c.-4375G>A| |
S136 |
8 | BAA01g09940 | A01 | 4450867 | A | C | upstream_gene_variant | MODIFIER | c.-4590T>G| |
S1 S103 S111 S131 S143 S145 S153 S164 S173 S181 S187 S242 S248 S263 S289 S295 S31 S36 S94 |
9 | BAA01g09940 | A01 | 4451060 | A | G | upstream_gene_variant | MODIFIER | c.-4783T>C| |
S117 S126 S134 S138 S157 S159 S181 S195 S26 S62 S68 S77 S79 S84 S94 |
10 | BAA01g09940 | A01 | 4451089 | C | T | upstream_gene_variant | MODIFIER | c.-4812G>A| |
S18 S305 |
11 | BAA01g09940 | A01 | 4451172 | A | G | upstream_gene_variant | MODIFIER | c.-4895T>C| |
S132 S170 S194 S227 S37 S87 |