Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g28400 | A10 | 21760206 | C | T | missense_variant | MODERATE | c.1736G>A|p.Arg579Lys |
S166 |
2 | BAA10g28400 | A10 | 21760308 | C | T | missense_variant | MODERATE | c.1634G>A|p.Gly545Glu |
S169 |
3 | BAA10g28400 | A10 | 21760687 | C | T | missense_variant | MODERATE | c.1255G>A|p.Glu419Lys |
S153 S213 |
4 | BAA10g28400 | A10 | 21760914 | C | T | missense_variant | MODERATE | c.1028G>A|p.Gly343Glu |
S204 |
5 | BAA10g28400 | A10 | 21761419 | C | T | missense_variant | MODERATE | c.523G>A|p.Gly175Arg |
S283 |
6 | BAA10g28400 | A10 | 21761753 | G | A | synonymous_variant | LOW | c.189C>T|p.Asp63Asp |
S64 |
7 | BAA10g28400 | A10 | 21763959 | G | A | upstream_gene_variant | MODIFIER | c.-2018C>T| |
S184 |
8 | BAA10g28400 | A10 | 21764047 | G | A | upstream_gene_variant | MODIFIER | c.-2106C>T| |
S54 |
9 | BAA10g28400 | A10 | 21764118 | G | A | upstream_gene_variant | MODIFIER | c.-2177C>T| |
S122 |
10 | BAA10g28400 | A10 | 21764153 | C | T | upstream_gene_variant | MODIFIER | c.-2212G>A| |
S188 |
11 | BAA10g28400 | A10 | 21764459 | C | T | upstream_gene_variant | MODIFIER | c.-2518G>A| |
S8 |
12 | BAA10g28400 | A10 | 21765477 | G | A | upstream_gene_variant | MODIFIER | c.-3536C>T| |
S263 |