Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g42340 | A02 | 35297447 | C | T | missense_variant | MODERATE | c.1019G>A|p.Ser340Asn |
S123 |
2 | BAA02g42340 | A02 | 35299501 | C | T | upstream_gene_variant | MODIFIER | c.-1036G>A| |
S112 |
3 | BAA02g42340 | A02 | 35299570 | C | T | upstream_gene_variant | MODIFIER | c.-1105G>A| |
S123 |
4 | BAA02g42340 | A02 | 35299582 | G | A | upstream_gene_variant | MODIFIER | c.-1117C>T| |
S5 |
5 | BAA02g42340 | A02 | 35300504 | C | T | upstream_gene_variant | MODIFIER | c.-2039G>A| |
S63 |
6 | BAA02g42340 | A02 | 35300539 | C | T | upstream_gene_variant | MODIFIER | c.-2074G>A| |
S107 |
7 | BAA02g42340 | A02 | 35301349 | C | T | upstream_gene_variant | MODIFIER | c.-2884G>A| |
S16 |
8 | BAA02g42340 | A02 | 35301439 | G | A | upstream_gene_variant | MODIFIER | c.-2974C>T| |
S251 |
9 | BAA02g42340 | A02 | 35303357 | G | A | upstream_gene_variant | MODIFIER | c.-4892C>T| |
S259 |