Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g00740 | A07 | 512383 | G | A | downstream_gene_variant | MODIFIER | c.*3887C>T| |
S237 |
2 | BAA07g00740 | A07 | 516349 | C | T | missense_variant | MODERATE | c.206G>A|p.Gly69Glu |
S260 |
3 | BAA07g00740 | A07 | 516588 | G | A | upstream_gene_variant | MODIFIER | c.-34C>T| |
S9 |
4 | BAA07g00740 | A07 | 518625 | C | T | upstream_gene_variant | MODIFIER | c.-2071G>A| |
S1 S90 |
5 | BAA07g00740 | A07 | 518685 | G | A | upstream_gene_variant | MODIFIER | c.-2131C>T| |
S171 |
6 | BAA07g00740 | A07 | 519317 | G | A | upstream_gene_variant | MODIFIER | c.-2763C>T| |
S296 |
7 | BAA07g00740 | A07 | 519487 | G | A | upstream_gene_variant | MODIFIER | c.-2933C>T| |
S275 |
8 | BAA07g00740 | A07 | 520665 | C | T | upstream_gene_variant | MODIFIER | c.-4111G>A| |
S281 |
9 | BAA07g00740 | A07 | 520730 | G | A | upstream_gene_variant | MODIFIER | c.-4176C>T| |
S117 |
10 | BAA07g00740 | A07 | 521222 | C | T | upstream_gene_variant | MODIFIER | c.-4668G>A| |
S280 |