Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g14800 | A02 | 6983763 | G | A | upstream_gene_variant | MODIFIER | c.-608G>A| |
S293 |
2 | BAA02g14800 | A02 | 6984389 | G | A | missense_variant | MODERATE | c.19G>A|p.Asp7Asn |
S291 |
3 | BAA02g14800 | A02 | 6984558 | C | T | missense_variant | MODERATE | c.188C>T|p.Ser63Phe |
S270 |
4 | BAA02g14800 | A02 | 6984999 | G | A | synonymous_variant | LOW | c.213G>A|p.Ala71Ala |
S205 |
5 | BAA02g14800 | A02 | 6985213 | C | T | synonymous_variant | LOW | c.427C>T|p.Leu143Leu |
S185 |
6 | BAA02g14800 | A02 | 6985334 | C | T | missense_variant | MODERATE | c.548C>T|p.Ser183Phe |
S308 |
7 | BAA02g14800 | A02 | 6985798 | C | T | missense_variant | MODERATE | c.943C>T|p.Pro315Ser |
S34 |
8 | BAA02g14800 | A02 | 6985807 | C | T | missense_variant | MODERATE | c.952C>T|p.Pro318Ser |
S79 S84 |
9 | BAA02g14800 | A02 | 6986340 | G | A | synonymous_variant | LOW | c.1332G>A|p.Glu444Glu |
S162 |
10 | BAA02g14800 | A02 | 6986851 | G | A | missense_variant | MODERATE | c.1843G>A|p.Glu615Lys |
S10 |