Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g46140 | A02 | 37597700 | C | T | missense_variant | MODERATE | c.485G>A|p.Ser162Asn |
S18 |
2 | BAA02g46140 | A02 | 37597838 | G | A | missense_variant | MODERATE | c.347C>T|p.Ser116Phe |
S169 |
3 | BAA02g46140 | A02 | 37598007 | G | A | missense_variant | MODERATE | c.178C>T|p.Leu60Phe |
S44 |
4 | BAA02g46140 | A02 | 37600231 | C | T | upstream_gene_variant | MODIFIER | c.-2047G>A| |
S263 |
5 | BAA02g46140 | A02 | 37600721 | G | A | upstream_gene_variant | MODIFIER | c.-2537C>T| |
S199 |
6 | BAA02g46140 | A02 | 37601127 | G | A | upstream_gene_variant | MODIFIER | c.-2943C>T| |
S245 |
7 | BAA02g46140 | A02 | 37601207 | G | A | upstream_gene_variant | MODIFIER | c.-3023C>T| |
S202 |
8 | BAA02g46140 | A02 | 37601583 | C | T | upstream_gene_variant | MODIFIER | c.-3399G>A| |
S296 |
9 | BAA02g46140 | A02 | 37601820 | C | T | upstream_gene_variant | MODIFIER | c.-3636G>A| |
S105 S106 |
10 | BAA02g46140 | A02 | 37602284 | C | T | upstream_gene_variant | MODIFIER | c.-4100G>A| |
S116 |