Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g03600 | A10 | 1730250 | G | A | missense_variant | MODERATE | c.992C>T|p.Thr331Ile |
S158 |
2 | BAA10g03600 | A10 | 1730949 | C | T | missense_variant | MODERATE | c.688G>A|p.Asp230Asn |
S297 |
3 | BAA10g03600 | A10 | 1731529 | C | T | synonymous_variant | LOW | c.555G>A|p.Lys185Lys |
S224 |
4 | BAA10g03600 | A10 | 1731581 | G | A | missense_variant | MODERATE | c.503C>T|p.Ala168Val |
S283 |
5 | BAA10g03600 | A10 | 1732377 | G | A | missense_variant | MODERATE | c.221C>T|p.Thr74Ile |
S20 |
6 | BAA10g03600 | A10 | 1732861 | C | T | missense_variant | MODERATE | c.52G>A|p.Val18Met |
S162 |
7 | BAA10g03600 | A10 | 1734895 | G | A | upstream_gene_variant | MODIFIER | c.-1983C>T| |
S292 |
8 | BAA10g03600 | A10 | 1735320 | G | A | upstream_gene_variant | MODIFIER | c.-2408C>T| |
S296 |
9 | BAA10g03600 | A10 | 1737702 | G | A | upstream_gene_variant | MODIFIER | c.-4790C>T| |
S20 |