Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g15890 | A10 | 16034556 | G | A | upstream_gene_variant | MODIFIER | c.-4014G>A| |
S209 |
2 | BAA10g15890 | A10 | 16035585 | G | A | upstream_gene_variant | MODIFIER | c.-2985G>A| |
S165 |
3 | BAA10g15890 | A10 | 16036526 | G | A | upstream_gene_variant | MODIFIER | c.-2044G>A| |
S9 |
4 | BAA10g15890 | A10 | 16036708 | C | T | upstream_gene_variant | MODIFIER | c.-1862C>T| |
S13 |
5 | BAA10g15890 | A10 | 16036997 | C | T | upstream_gene_variant | MODIFIER | c.-1573C>T| |
S8 |
6 | BAA10g15890 | A10 | 16037534 | G | A | upstream_gene_variant | MODIFIER | c.-1036G>A| |
S25 |
7 | BAA10g15890 | A10 | 16038418 | C | T | upstream_gene_variant | MODIFIER | c.-152C>T| |
S305 |
8 | BAA10g15890 | A10 | 16038645 | C | T | missense_variant | MODERATE | c.76C>T|p.Pro26Ser |
S25 |
9 | BAA10g15890 | A10 | 16039431 | C | T | synonymous_variant | LOW | c.420C>T|p.Phe140Phe |
S210 S225 |