Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g23490 | A09 | 14905390 | C | T | upstream_gene_variant | MODIFIER | c.-593C>T| |
S64 |
2 | BAA09g23490 | A09 | 14907590 | G | A | missense_variant | MODERATE | c.544G>A|p.Asp182Asn |
S7 |
3 | BAA09g23490 | A09 | 14908833 | C | T | missense_variant | MODERATE | c.1354C>T|p.Pro452Ser |
S242 |
4 | BAA09g23490 | A09 | 14909006 | C | T | synonymous_variant | LOW | c.1527C>T|p.Val509Val |
S135 |
5 | BAA09g23490 | A09 | 14909489 | G | A | missense_variant | MODERATE | c.1728G>A|p.Met576Ile |
S100 |
6 | BAA09g23490 | A09 | 14909782 | C | T | missense_variant | MODERATE | c.2021C>T|p.Ser674Leu |
S211 S227 |
7 | BAA09g23490 | A09 | 14910201 | G | A | missense_variant | MODERATE | c.2291G>A|p.Cys764Tyr |
S244 |
8 | BAA09g23490 | A09 | 14910660 | C | T | downstream_gene_variant | MODIFIER | c.*272C>T| |
S272 |
9 | BAA09g23490 | A09 | 14910786 | G | A | downstream_gene_variant | MODIFIER | c.*398G>A| |
S291 |
10 | BAA09g23490 | A09 | 14910908 | C | T | downstream_gene_variant | MODIFIER | c.*520C>T| |
S286 |