Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g21170 | A07 | 26036122 | C | T | upstream_gene_variant | MODIFIER | c.-3802C>T| |
S213 |
2 | BAA07g21170 | A07 | 26036375 | G | A | upstream_gene_variant | MODIFIER | c.-3549G>A| |
S171 |
3 | BAA07g21170 | A07 | 26036879 | G | A | upstream_gene_variant | MODIFIER | c.-3045G>A| |
S158 |
4 | BAA07g21170 | A07 | 26037612 | C | T | upstream_gene_variant | MODIFIER | c.-2312C>T| |
S264 |
5 | BAA07g21170 | A07 | 26037734 | C | T | upstream_gene_variant | MODIFIER | c.-2190C>T| |
S8 |
6 | BAA07g21170 | A07 | 26039238 | C | T | upstream_gene_variant | MODIFIER | c.-686C>T| |
S56 |
7 | BAA07g21170 | A07 | 26039903 | G | A | upstream_gene_variant | MODIFIER | c.-21G>A| |
S223 |
8 | BAA07g21170 | A07 | 26039998 | C | T | synonymous_variant | LOW | c.75C>T|p.Asp25Asp |
S12 |
9 | BAA07g21170 | A07 | 26041629 | C | T | downstream_gene_variant | MODIFIER | c.*1031C>T| |
S136 |