Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g19590 | A10 | 17918422 | G | A | upstream_gene_variant | MODIFIER | c.-2039G>A| |
S57 |
2 | BAA10g19590 | A10 | 17919005 | C | T | upstream_gene_variant | MODIFIER | c.-1456C>T| |
S169 |
3 | BAA10g19590 | A10 | 17923692 | G | A | missense_variant | MODERATE | c.1682G>A|p.Gly561Glu |
S160 |
4 | BAA10g19590 | A10 | 17923796 | G | A | missense_variant | MODERATE | c.1786G>A|p.Ala596Thr |
S219 |
5 | BAA10g19590 | A10 | 17924246 | C | T | synonymous_variant | LOW | c.2025C>T|p.Cys675Cys |
S107 |
6 | BAA10g19590 | A10 | 17924408 | C | T | synonymous_variant | LOW | c.2100C>T|p.Phe700Phe |
S130 |
7 | BAA10g19590 | A10 | 17924722 | G | A | missense_variant | MODERATE | c.2305G>A|p.Glu769Lys |
S280 |
8 | BAA10g19590 | A10 | 17924904 | G | A | missense_variant | MODERATE | c.2344G>A|p.Glu782Lys |
S67 |
9 | BAA10g19590 | A10 | 17926145 | G | A | downstream_gene_variant | MODIFIER | c.*1125G>A| |
S95 |
10 | BAA10g19590 | A10 | 17927278 | G | A | downstream_gene_variant | MODIFIER | c.*2258G>A| |
S273 |
11 | BAA10g19590 | A10 | 17927900 | G | A | downstream_gene_variant | MODIFIER | c.*2880G>A| |
S279 |