Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g68760 | A09 | 61697792 | C | T | missense_variant | MODERATE | c.1580G>A|p.Ser527Asn |
S203 |
2 | BAA09g68760 | A09 | 61697798 | C | T | missense_variant | MODERATE | c.1574G>A|p.Gly525Glu |
S20 |
3 | BAA09g68760 | A09 | 61697990 | C | T | missense_variant | MODERATE | c.1456G>A|p.Ala486Thr |
S198 |
4 | BAA09g68760 | A09 | 61700231 | C | T | upstream_gene_variant | MODIFIER | c.-301G>A| |
S155 S211 |
5 | BAA09g68760 | A09 | 61700586 | C | T | upstream_gene_variant | MODIFIER | c.-656G>A| |
S88 |
6 | BAA09g68760 | A09 | 61701586 | G | A | upstream_gene_variant | MODIFIER | c.-1656C>T| |
S28 |
7 | BAA09g68760 | A09 | 61701646 | G | A | upstream_gene_variant | MODIFIER | c.-1716C>T| |
S10 |
8 | BAA09g68760 | A09 | 61701652 | G | A | upstream_gene_variant | MODIFIER | c.-1722C>T| |
S265 |
9 | BAA09g68760 | A09 | 61703878 | C | T | upstream_gene_variant | MODIFIER | c.-3948G>A| |
S179 |