Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g29060 | A10 | 22017107 | C | T | synonymous_variant | LOW | c.1260G>A|p.Gly420Gly |
S168 |
2 | BAA10g29060 | A10 | 22017411 | C | T | missense_variant | MODERATE | c.956G>A|p.Gly319Glu |
S243 |
3 | BAA10g29060 | A10 | 22018895 | C | T | missense_variant | MODERATE | c.4G>A|p.Gly2Ser |
S286 |
4 | BAA10g29060 | A10 | 22019682 | G | A | upstream_gene_variant | MODIFIER | c.-784C>T| |
S219 S72 |
5 | BAA10g29060 | A10 | 22020698 | C | T | upstream_gene_variant | MODIFIER | c.-1800G>A| |
S47 |
6 | BAA10g29060 | A10 | 22021054 | G | A | upstream_gene_variant | MODIFIER | c.-2156C>T| |
S240 |
7 | BAA10g29060 | A10 | 22021394 | C | A | upstream_gene_variant | MODIFIER | c.-2496G>T| |
S158 |
8 | BAA10g29060 | A10 | 22021838 | C | T | upstream_gene_variant | MODIFIER | c.-2940G>A| |
S204 |
9 | BAA10g29060 | A10 | 22023298 | C | T | upstream_gene_variant | MODIFIER | c.-4400G>A| |
S286 |
10 | BAA10g29060 | A10 | 22023454 | G | A | upstream_gene_variant | MODIFIER | c.-4556C>T| |
S32 |
11 | BAA10g29060 | A10 | 22023601 | G | A | upstream_gene_variant | MODIFIER | c.-4703C>T| |
S79 S84 |