Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g19720 | A02 | 10265768 | C | G | missense_variant | MODERATE | c.541G>C|p.Ala181Pro |
S278 |
2 | BAA02g19720 | A02 | 10266069 | G | A | missense_variant | MODERATE | c.334C>T|p.Arg112Cys |
S291 |
3 | BAA02g19720 | A02 | 10266209 | C | T | missense_variant | MODERATE | c.194G>A|p.Arg65Lys |
S299 |
4 | BAA02g19720 | A02 | 10267072 | G | A | upstream_gene_variant | MODIFIER | c.-593C>T| |
S35 |
5 | BAA02g19720 | A02 | 10267322 | C | T | upstream_gene_variant | MODIFIER | c.-843G>A| |
S305 |
6 | BAA02g19720 | A02 | 10267757 | G | A | upstream_gene_variant | MODIFIER | c.-1278C>T| |
S237 |
7 | BAA02g19720 | A02 | 10268664 | G | A | upstream_gene_variant | MODIFIER | c.-2185C>T| |
S34 |
8 | BAA02g19720 | A02 | 10269039 | G | A | upstream_gene_variant | MODIFIER | c.-2560C>T| |
S59 |
9 | BAA02g19720 | A02 | 10269611 | G | A | upstream_gene_variant | MODIFIER | c.-3132C>T| |
S19 |
10 | BAA02g19720 | A02 | 10270460 | G | A | upstream_gene_variant | MODIFIER | c.-3981C>T| |
S225 |
11 | BAA02g19720 | A02 | 10270629 | T | C | upstream_gene_variant | MODIFIER | c.-4150A>G| |
S182 |