Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g15840 | A02 | 7704647 | C | T | upstream_gene_variant | MODIFIER | c.-4199C>T| |
S218 |
2 | BAA02g15840 | A02 | 7707543 | G | A | upstream_gene_variant | MODIFIER | c.-1303G>A| |
S125 |
3 | BAA02g15840 | A02 | 7707974 | G | A | upstream_gene_variant | MODIFIER | c.-872G>A| |
S87 |
4 | BAA02g15840 | A02 | 7708067 | C | T | upstream_gene_variant | MODIFIER | c.-779C>T| |
S270 |
5 | BAA02g15840 | A02 | 7708309 | A | C | upstream_gene_variant | MODIFIER | c.-537A>C| |
S134 |
6 | BAA02g15840 | A02 | 7708395 | G | A | upstream_gene_variant | MODIFIER | c.-451G>A| |
S10 |
7 | BAA02g15840 | A02 | 7711112 | G | A | splice_region_variant&synonymous_variant | LOW | c.1200G>A|p.Glu400Glu |
S146 |
8 | BAA02g15840 | A02 | 7711240 | G | A | missense_variant | MODERATE | c.1226G>A|p.Arg409His |
S126 |
9 | BAA02g15840 | A02 | 7711667 | C | T | missense_variant | MODERATE | c.1442C>T|p.Thr481Ile |
S139 |
10 | BAA02g15840 | A02 | 7711946 | G | A | missense_variant | MODERATE | c.1582G>A|p.Gly528Arg |
S308 |
11 | BAA02g15840 | A02 | 7713061 | C | T | synonymous_variant | LOW | c.2250C>T|p.Ile750Ile |
S40 S49 |