Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g20100 | A02 | 10600978 | G | A | synonymous_variant | LOW | c.2553C>T|p.Asn851Asn |
S19 |
2 | BAA02g20100 | A02 | 10601116 | G | A | synonymous_variant | LOW | c.2415C>T|p.Pro805Pro |
S67 |
3 | BAA02g20100 | A02 | 10601516 | G | A | missense_variant | MODERATE | c.2015C>T|p.Ser672Phe |
S159 S243 |
4 | BAA02g20100 | A02 | 10601711 | G | A | missense_variant | MODERATE | c.1820C>T|p.Ser607Phe |
S264 |
5 | BAA02g20100 | A02 | 10602542 | C | T | missense_variant | MODERATE | c.1075G>A|p.Asp359Asn |
S75 S81 |
6 | BAA02g20100 | A02 | 10602741 | C | T | synonymous_variant | LOW | c.876G>A|p.Gln292Gln |
S108 |
7 | BAA02g20100 | A02 | 10603626 | C | T | upstream_gene_variant | MODIFIER | c.-10G>A| |
S277 |
8 | BAA02g20100 | A02 | 10605632 | C | T | upstream_gene_variant | MODIFIER | c.-2016G>A| |
S184 |
9 | BAA02g20100 | A02 | 10606144 | C | T | upstream_gene_variant | MODIFIER | c.-2528G>A| |
S267 |
10 | BAA02g20100 | A02 | 10607087 | C | T | upstream_gene_variant | MODIFIER | c.-3471G>A| |
S32 |