Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g29680 | A08 | 20300970 | G | A | upstream_gene_variant | MODIFIER | c.-2104G>A| |
S216 |
2 | BAA08g29680 | A08 | 20302812 | G | A | upstream_gene_variant | MODIFIER | c.-262G>A| |
S142 |
3 | BAA08g29680 | A08 | 20303391 | C | T | missense_variant | MODERATE | c.229C>T|p.Leu77Phe |
S105 S106 |
4 | BAA08g29680 | A08 | 20303637 | G | A | missense_variant | MODERATE | c.304G>A|p.Glu102Lys |
S62 |
5 | BAA08g29680 | A08 | 20303709 | G | A | missense_variant | MODERATE | c.376G>A|p.Asp126Asn |
S183 |
6 | BAA08g29680 | A08 | 20303882 | G | A | missense_variant&splice_region_variant | MODERATE | c.395G>A|p.Gly132Glu |
S36 |
7 | BAA08g29680 | A08 | 20305810 | G | A | missense_variant | MODERATE | c.1408G>A|p.Glu470Lys |
S107 |
8 | BAA08g29680 | A08 | 20306802 | C | T | missense_variant | MODERATE | c.1700C>T|p.Ala567Val |
S28 |
9 | BAA08g29680 | A08 | 20310736 | C | T | downstream_gene_variant | MODIFIER | c.*2403C>T| |
S173 |