Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g16460 | A01 | 7996567 | G | A | missense_variant | MODERATE | c.152C>T|p.Thr51Ile |
S156 |
2 | BAA01g16460 | A01 | 7999067 | G | A | upstream_gene_variant | MODIFIER | c.-2349C>T| |
S85 |
3 | BAA01g16460 | A01 | 7999332 | C | T | upstream_gene_variant | MODIFIER | c.-2614G>A| |
S1 S90 |
4 | BAA01g16460 | A01 | 7999632 | G | A | upstream_gene_variant | MODIFIER | c.-2914C>T| |
S201 |
5 | BAA01g16460 | A01 | 7999893 | C | T | upstream_gene_variant | MODIFIER | c.-3175G>A| |
S198 |
6 | BAA01g16460 | A01 | 8000048 | C | T | upstream_gene_variant | MODIFIER | c.-3330G>A| |
S192 |
7 | BAA01g16460 | A01 | 8000226 | C | T | upstream_gene_variant | MODIFIER | c.-3508G>A| |
S2 |
8 | BAA01g16460 | A01 | 8000331 | G | A | upstream_gene_variant | MODIFIER | c.-3613C>T| |
S117 |
9 | BAA01g16460 | A01 | 8000381 | G | A | upstream_gene_variant | MODIFIER | c.-3663C>T| |
S213 |
10 | BAA01g16460 | A01 | 8001162 | C | T | upstream_gene_variant | MODIFIER | c.-4444G>A| |
S125 |
11 | BAA01g16460 | A01 | 8001207 | C | T | upstream_gene_variant | MODIFIER | c.-4489G>A| |
S8 |
12 | BAA01g16460 | A01 | 8001501 | C | T | upstream_gene_variant | MODIFIER | c.-4783G>A| |
S269 |