Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g39650 | A02 | 33652201 | C | T | missense_variant | MODERATE | c.3244G>A|p.Val1082Ile |
S262 |
2 | BAA02g39650 | A02 | 33652381 | G | A | missense_variant | MODERATE | c.3064C>T|p.Pro1022Ser |
S268 |
3 | BAA02g39650 | A02 | 33652906 | C | T | missense_variant | MODERATE | c.2539G>A|p.Glu847Lys |
S68 |
4 | BAA02g39650 | A02 | 33653472 | G | A | synonymous_variant | LOW | c.2055C>T|p.Ser685Ser |
S45 |
5 | BAA02g39650 | A02 | 33654037 | G | A | missense_variant | MODERATE | c.1490C>T|p.Ala497Val |
S107 |
6 | BAA02g39650 | A02 | 33654220 | G | A | missense_variant | MODERATE | c.1307C>T|p.Ser436Phe |
S269 |
7 | BAA02g39650 | A02 | 33654308 | C | T | missense_variant | MODERATE | c.1219G>A|p.Asp407Asn |
S133 |
8 | BAA02g39650 | A02 | 33656447 | G | A | upstream_gene_variant | MODIFIER | c.-419C>T| |
S288 |
9 | BAA02g39650 | A02 | 33656924 | G | A | upstream_gene_variant | MODIFIER | c.-896C>T| |
S67 |
10 | BAA02g39650 | A02 | 33658717 | G | A | upstream_gene_variant | MODIFIER | c.-2689C>T| |
S203 |
11 | BAA02g39650 | A02 | 33659897 | G | A | upstream_gene_variant | MODIFIER | c.-3869C>T| |
S302 |
12 | BAA02g39650 | A02 | 33660380 | G | A | upstream_gene_variant | MODIFIER | c.-4352C>T| |
S207 |