Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g17070 | A02 | 8497111 | C | T | downstream_gene_variant | MODIFIER | c.*1828G>A| |
S273 |
2 | BAA02g17070 | A02 | 8499425 | C | T | stop_gained | HIGH | c.1659G>A|p.Trp553* |
S1 S90 |
3 | BAA02g17070 | A02 | 8502827 | C | T | missense_variant | MODERATE | c.284G>A|p.Gly95Glu |
S164 |
4 | BAA02g17070 | A02 | 8502834 | C | T | missense_variant | MODERATE | c.277G>A|p.Asp93Asn |
S76 |
5 | BAA02g17070 | A02 | 8502850 | G | A | synonymous_variant | LOW | c.261C>T|p.Phe87Phe |
S228 |
6 | BAA02g17070 | A02 | 8503371 | G | A | missense_variant | MODERATE | c.35C>T|p.Ser12Phe |
S177 |
7 | BAA02g17070 | A02 | 8503626 | G | A | upstream_gene_variant | MODIFIER | c.-221C>T| |
S166 |
8 | BAA02g17070 | A02 | 8504461 | C | T | upstream_gene_variant | MODIFIER | c.-1056G>A| |
S32 |
9 | BAA02g17070 | A02 | 8506048 | C | T | upstream_gene_variant | MODIFIER | c.-2643G>A| |
S208 S219 |
10 | BAA02g17070 | A02 | 8506892 | G | A | upstream_gene_variant | MODIFIER | c.-3487C>T| |
S69 |
11 | BAA02g17070 | A02 | 8508197 | C | T | upstream_gene_variant | MODIFIER | c.-4792G>A| |
S70 |