Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g19840 | A10 | 18058226 | G | A | synonymous_variant | LOW | c.855C>T|p.Tyr285Tyr |
S64 |
2 | BAA10g19840 | A10 | 18058366 | C | T | missense_variant | MODERATE | c.715G>A|p.Asp239Asn |
S183 |
3 | BAA10g19840 | A10 | 18060491 | G | A | missense_variant | MODERATE | c.34C>T|p.Pro12Ser |
S197 |
4 | BAA10g19840 | A10 | 18063759 | C | T | upstream_gene_variant | MODIFIER | c.-3235G>A| |
S206 |
5 | BAA10g19840 | A10 | 18063976 | G | A | upstream_gene_variant | MODIFIER | c.-3452C>T| |
S158 |
6 | BAA10g19840 | A10 | 18064174 | C | T | upstream_gene_variant | MODIFIER | c.-3650G>A| |
S162 |
7 | BAA10g19840 | A10 | 18064325 | C | T | upstream_gene_variant | MODIFIER | c.-3801G>A| |
S124 |