Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g11180 | A05 | 5667783 | C | T | upstream_gene_variant | MODIFIER | c.-1552C>T| |
S36 |
2 | BAA05g11180 | A05 | 5667918 | C | T | upstream_gene_variant | MODIFIER | c.-1417C>T| |
S5 |
3 | BAA05g11180 | A05 | 5668554 | G | A | upstream_gene_variant | MODIFIER | c.-781G>A| |
S178 |
4 | BAA05g11180 | A05 | 5670384 | C | T | missense_variant | MODERATE | c.980C>T|p.Pro327Leu |
S209 |
5 | BAA05g11180 | A05 | 5670857 | G | A | missense_variant&splice_region_variant | MODERATE | c.1310G>A|p.Gly437Asp |
S133 |
6 | BAA05g11180 | A05 | 5671305 | G | A | stop_gained&splice_region_variant | HIGH | c.1596G>A|p.Trp532* |
S67 |
7 | BAA05g11180 | A05 | 5671391 | G | A | missense_variant | MODERATE | c.1682G>A|p.Arg561Lys |
S32 |
8 | BAA05g11180 | A05 | 5671470 | C | T | synonymous_variant | LOW | c.1761C>T|p.Asp587Asp |
S242 |