Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g29970 | A05 | 33239420 | C | T | missense_variant | MODERATE | c.3004G>A|p.Gly1002Arg |
S12 |
2 | BAA05g29970 | A05 | 33239953 | G | A | missense_variant | MODERATE | c.2665C>T|p.Leu889Phe |
S168 |
3 | BAA05g29970 | A05 | 33240923 | C | T | missense_variant | MODERATE | c.2026G>A|p.Asp676Asn |
S164 |
4 | BAA05g29970 | A05 | 33241037 | G | A | missense_variant | MODERATE | c.1912C>T|p.Pro638Ser |
S218 |
5 | BAA05g29970 | A05 | 33242682 | G | A | missense_variant | MODERATE | c.529C>T|p.Pro177Ser |
S173 |
6 | BAA05g29970 | A05 | 33243098 | C | T | missense_variant | MODERATE | c.113G>A|p.Ser38Asn |
S94 |
7 | BAA05g29970 | A05 | 33243488 | C | T | upstream_gene_variant | MODIFIER | c.-278G>A| |
S114 |
8 | BAA05g29970 | A05 | 33243618 | G | A | upstream_gene_variant | MODIFIER | c.-408C>T| |
S128 |
9 | BAA05g29970 | A05 | 33244070 | C | T | upstream_gene_variant | MODIFIER | c.-860G>A| |
S251 |
10 | BAA05g29970 | A05 | 33248153 | C | T | upstream_gene_variant | MODIFIER | c.-4943G>A| |
S236 |