Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g20390 | A10 | 18370474 | G | A | upstream_gene_variant | MODIFIER | c.-420G>A| |
S233 |
2 | BAA10g20390 | A10 | 18372986 | G | A | missense_variant | MODERATE | c.514G>A|p.Asp172Asn |
S263 |
3 | BAA10g20390 | A10 | 18373568 | C | T | missense_variant | MODERATE | c.905C>T|p.Ala302Val |
S12 |
4 | BAA10g20390 | A10 | 18373590 | C | T | synonymous_variant | LOW | c.927C>T|p.Ile309Ile |
S286 |
5 | BAA10g20390 | A10 | 18373656 | C | T | synonymous_variant | LOW | c.993C>T|p.Pro331Pro |
S183 |