Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g39400 | A09 | 47034585 | G | A | downstream_gene_variant | MODIFIER | c.*3512C>T| |
S111 |
2 | BAA09g39400 | A09 | 47035918 | C | T | downstream_gene_variant | MODIFIER | c.*2179G>A| |
S303 |
3 | BAA09g39400 | A09 | 47039233 | G | A | missense_variant | MODERATE | c.727C>T|p.Pro243Ser |
S266 |
4 | BAA09g39400 | A09 | 47039474 | C | T | synonymous_variant | LOW | c.486G>A|p.Gly162Gly |
S250 |
5 | BAA09g39400 | A09 | 47041467 | G | A | upstream_gene_variant | MODIFIER | c.-1508C>T| |
S284 |
6 | BAA09g39400 | A09 | 47041945 | C | T | upstream_gene_variant | MODIFIER | c.-1986G>A| |
S241 |
7 | BAA09g39400 | A09 | 47042392 | G | A | upstream_gene_variant | MODIFIER | c.-2433C>T| |
S105 S106 |