Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g18700 | A09 | 11251940 | C | T | upstream_gene_variant | MODIFIER | c.-4306C>T| |
S68 |
2 | BAA09g18700 | A09 | 11252156 | C | T | upstream_gene_variant | MODIFIER | c.-4090C>T| |
S115 |
3 | BAA09g18700 | A09 | 11253895 | C | T | upstream_gene_variant | MODIFIER | c.-2351C>T| |
S148 S210 |
4 | BAA09g18700 | A09 | 11254120 | G | A | upstream_gene_variant | MODIFIER | c.-2126G>A| |
S84 S93 |
5 | BAA09g18700 | A09 | 11254592 | A | G | upstream_gene_variant | MODIFIER | c.-1654A>G| |
S203 |
6 | BAA09g18700 | A09 | 11254644 | C | A | upstream_gene_variant | MODIFIER | c.-1602C>A| |
S123 |
7 | BAA09g18700 | A09 | 11255182 | C | T | upstream_gene_variant | MODIFIER | c.-1064C>T| |
S115 |
8 | BAA09g18700 | A09 | 11256255 | G | A | missense_variant | MODERATE | c.10G>A|p.Asp4Asn |
S308 |
9 | BAA09g18700 | A09 | 11260666 | G | A | downstream_gene_variant | MODIFIER | c.*4262G>A| |
S34 |