Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g69140 | A09 | 61843421 | G | A | missense_variant | MODERATE | c.23G>A|p.Gly8Glu |
S295 |
2 | BAA09g69140 | A09 | 61844032 | T | C | missense_variant | MODERATE | c.356T>C|p.Phe119Ser |
S268 |
3 | BAA09g69140 | A09 | 61844439 | G | A | missense_variant | MODERATE | c.650G>A|p.Gly217Asp |
S283 |
4 | BAA09g69140 | A09 | 61845118 | G | A | synonymous_variant | LOW | c.1227G>A|p.Lys409Lys |
S68 |
5 | BAA09g69140 | A09 | 61845316 | G | A | synonymous_variant | LOW | c.1320G>A|p.Lys440Lys |
S57 |
6 | BAA09g69140 | A09 | 61846581 | C | T | downstream_gene_variant | MODIFIER | c.*878C>T| |
S77 S82 |
7 | BAA09g69140 | A09 | 61847134 | C | A | downstream_gene_variant | MODIFIER | c.*1431C>A| |
S134 S193 |
8 | BAA09g69140 | A09 | 61847152 | C | T | downstream_gene_variant | MODIFIER | c.*1449C>T| |
S223 |
9 | BAA09g69140 | A09 | 61847277 | C | T | downstream_gene_variant | MODIFIER | c.*1574C>T| |
S228 |