Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g10020 | A07 | 18966499 | C | T | upstream_gene_variant | MODIFIER | c.-3298C>T| |
S18 |
2 | BAA07g10020 | A07 | 18966785 | C | T | upstream_gene_variant | MODIFIER | c.-3012C>T| |
S113 |
3 | BAA07g10020 | A07 | 18967318 | A | C | upstream_gene_variant | MODIFIER | c.-2479A>C| |
S112 |
4 | BAA07g10020 | A07 | 18967493 | C | T | upstream_gene_variant | MODIFIER | c.-2304C>T| |
S75 S81 |
5 | BAA07g10020 | A07 | 18967788 | C | T | upstream_gene_variant | MODIFIER | c.-2009C>T| |
S11 |
6 | BAA07g10020 | A07 | 18968246 | C | T | upstream_gene_variant | MODIFIER | c.-1551C>T| |
S166 |
7 | BAA07g10020 | A07 | 18971010 | C | T | missense_variant | MODERATE | c.578C>T|p.Ala193Val |
S68 |
8 | BAA07g10020 | A07 | 18971800 | C | T | missense_variant | MODERATE | c.871C>T|p.Leu291Phe |
S120 |
9 | BAA07g10020 | A07 | 18972048 | C | T | missense_variant | MODERATE | c.995C>T|p.Ala332Val |
S277 |