Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g24130 | A10 | 19995901 | G | A | missense_variant | MODERATE | c.310C>T|p.Leu104Phe |
S172 S217 |
2 | BAA10g24130 | A10 | 19996139 | G | A | synonymous_variant | LOW | c.72C>T|p.Leu24Leu |
S69 |
3 | BAA10g24130 | A10 | 19997458 | G | A | upstream_gene_variant | MODIFIER | c.-1248C>T| |
S9 |
4 | BAA10g24130 | A10 | 19998045 | C | T | upstream_gene_variant | MODIFIER | c.-1835G>A| |
S152 |
5 | BAA10g24130 | A10 | 19998549 | C | T | upstream_gene_variant | MODIFIER | c.-2339G>A| |
S274 |
6 | BAA10g24130 | A10 | 19998690 | G | A | upstream_gene_variant | MODIFIER | c.-2480C>T| |
S293 |
7 | BAA10g24130 | A10 | 19999129 | C | G | upstream_gene_variant | MODIFIER | c.-2919G>C| |
S105 S107 S125 S127 S129 S203 S237 S250 S298 S38 S48 S66 |
8 | BAA10g24130 | A10 | 20001052 | G | A | upstream_gene_variant | MODIFIER | c.-4842C>T| |
S66 |