Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g41970 | A03 | 19789983 | C | T | missense_variant | MODERATE | c.521C>T|p.Pro174Leu |
S42 |
2 | BAA03g41970 | A03 | 19790372 | G | A | missense_variant | MODERATE | c.844G>A|p.Glu282Lys |
S212 |
3 | BAA03g41970 | A03 | 19790528 | G | A | missense_variant | MODERATE | c.1000G>A|p.Asp334Asn |
S185 |
4 | BAA03g41970 | A03 | 19790759 | C | T | missense_variant | MODERATE | c.1231C>T|p.Pro411Ser |
S240 |
5 | BAA03g41970 | A03 | 19790777 | G | A | missense_variant | MODERATE | c.1249G>A|p.Glu417Lys |
S177 |
6 | BAA03g41970 | A03 | 19791208 | C | T | synonymous_variant | LOW | c.1680C>T|p.Leu560Leu |
S204 |
7 | BAA03g41970 | A03 | 19793099 | G | A | downstream_gene_variant | MODIFIER | c.*1855G>A| |
S180 |
8 | BAA03g41970 | A03 | 19793853 | C | T | downstream_gene_variant | MODIFIER | c.*2609C>T| |
S19 |
9 | BAA03g41970 | A03 | 19795055 | C | T | downstream_gene_variant | MODIFIER | c.*3811C>T| |
S18 |
10 | BAA03g41970 | A03 | 19795686 | G | A | downstream_gene_variant | MODIFIER | c.*4442G>A| |
S23 |