Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g00880 | A10 | 410220 | G | A | upstream_gene_variant | MODIFIER | c.-1721G>A| |
S69 |
2 | BAA10g00880 | A10 | 411021 | C | T | upstream_gene_variant | MODIFIER | c.-920C>T| |
S185 |
3 | BAA10g00880 | A10 | 411069 | C | T | upstream_gene_variant | MODIFIER | c.-872C>T| |
S221 |
4 | BAA10g00880 | A10 | 411858 | C | T | upstream_gene_variant | MODIFIER | c.-83C>T| |
S244 |
5 | BAA10g00880 | A10 | 413371 | G | A | missense_variant | MODERATE | c.575G>A|p.Gly192Glu |
S3 |
6 | BAA10g00880 | A10 | 414317 | A | C | missense_variant | MODERATE | c.1069A>C|p.Asn357His |
S118 S12 S122 S128 S144 S164 S260 S266 S53 S8 |