Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g16190 | A10 | 16131509 | C | T | missense_variant | MODERATE | c.2456G>A|p.Gly819Asp |
S204 |
2 | BAA10g16190 | A10 | 16132000 | C | T | synonymous_variant | LOW | c.1965G>A|p.Lys655Lys |
S269 |
3 | BAA10g16190 | A10 | 16132066 | G | A | synonymous_variant | LOW | c.1899C>T|p.Gly633Gly |
S240 |
4 | BAA10g16190 | A10 | 16132083 | C | T | missense_variant | MODERATE | c.1882G>A|p.Glu628Lys |
S110 |
5 | BAA10g16190 | A10 | 16132397 | G | A | missense_variant | MODERATE | c.1568C>T|p.Ala523Val |
S207 |
6 | BAA10g16190 | A10 | 16133458 | G | A | synonymous_variant | LOW | c.507C>T|p.Val169Val |
S178 |
7 | BAA10g16190 | A10 | 16134034 | C | T | missense_variant | MODERATE | c.167G>A|p.Arg56Lys |
S272 |
8 | BAA10g16190 | A10 | 16136183 | C | T | upstream_gene_variant | MODIFIER | c.-1983G>A| |
S123 |
9 | BAA10g16190 | A10 | 16136451 | C | G | upstream_gene_variant | MODIFIER | c.-2251G>C| |
S5 |
10 | BAA10g16190 | A10 | 16138087 | C | T | upstream_gene_variant | MODIFIER | c.-3887G>A| |
S284 |
11 | BAA10g16190 | A10 | 16138861 | T | A | upstream_gene_variant | MODIFIER | c.-4661A>T| |
S262 |