Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g47640 | A09 | 51822094 | T | C | downstream_gene_variant | MODIFIER | c.*2779A>G| |
S203 |
2 | BAA09g47640 | A09 | 51822642 | G | A | downstream_gene_variant | MODIFIER | c.*2231C>T| |
S233 |
3 | BAA09g47640 | A09 | 51824890 | G | A | missense_variant | MODERATE | c.496C>T|p.Leu166Phe |
S42 |
4 | BAA09g47640 | A09 | 51826522 | G | A | upstream_gene_variant | MODIFIER | c.-321C>T| |
S201 |
5 | BAA09g47640 | A09 | 51826760 | G | A | upstream_gene_variant | MODIFIER | c.-559C>T| |
S165 |
6 | BAA09g47640 | A09 | 51826796 | G | A | upstream_gene_variant | MODIFIER | c.-595C>T| |
S308 |
7 | BAA09g47640 | A09 | 51829338 | C | T | upstream_gene_variant | MODIFIER | c.-3137G>A| |
S92 |
8 | BAA09g47640 | A09 | 51830000 | G | A | upstream_gene_variant | MODIFIER | c.-3799C>T| |
S105 S106 |
9 | BAA09g47640 | A09 | 51830172 | G | A | upstream_gene_variant | MODIFIER | c.-3971C>T| |
S165 |
10 | BAA09g47640 | A09 | 51830887 | G | A | upstream_gene_variant | MODIFIER | c.-4686C>T| |
S189 |