Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g19380 | A02 | 10041550 | G | A | upstream_gene_variant | MODIFIER | c.-2897G>A| |
S173 |
2 | BAA02g19380 | A02 | 10042381 | C | T | upstream_gene_variant | MODIFIER | c.-2066C>T| |
S242 |
3 | BAA02g19380 | A02 | 10043202 | G | A | upstream_gene_variant | MODIFIER | c.-1245G>A| |
S204 |
4 | BAA02g19380 | A02 | 10043313 | A | C | upstream_gene_variant | MODIFIER | c.-1134A>C| |
S41 |
5 | BAA02g19380 | A02 | 10043530 | C | T | upstream_gene_variant | MODIFIER | c.-917C>T| |
S163 |
6 | BAA02g19380 | A02 | 10043641 | G | A | upstream_gene_variant | MODIFIER | c.-806G>A| |
S169 |
7 | BAA02g19380 | A02 | 10043669 | C | T | upstream_gene_variant | MODIFIER | c.-778C>T| |
S185 |
8 | BAA02g19380 | A02 | 10044543 | C | T | missense_variant | MODERATE | c.97C>T|p.Leu33Phe |
S178 |
9 | BAA02g19380 | A02 | 10044717 | C | T | synonymous_variant | LOW | c.271C>T|p.Leu91Leu |
S266 |
10 | BAA02g19380 | A02 | 10045202 | C | T | synonymous_variant | LOW | c.756C>T|p.Leu252Leu |
S186 |
11 | BAA02g19380 | A02 | 10045652 | G | A | downstream_gene_variant | MODIFIER | c.*111G>A| |
S132 S215 S89 |