Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g54670 | A09 | 55199826 | C | T | missense_variant | MODERATE | c.3122G>A|p.Gly1041Glu |
S118 |
2 | BAA09g54670 | A09 | 55200257 | G | A | missense_variant | MODERATE | c.2909C>T|p.Ala970Val |
S34 |
3 | BAA09g54670 | A09 | 55201140 | G | A | missense_variant | MODERATE | c.2551C>T|p.Pro851Ser |
S88 |
4 | BAA09g54670 | A09 | 55201208 | C | T | missense_variant | MODERATE | c.2483G>A|p.Gly828Glu |
S136 |
5 | BAA09g54670 | A09 | 55201983 | G | A | synonymous_variant | LOW | c.1974C>T|p.Cys658Cys |
S221 |
6 | BAA09g54670 | A09 | 55203314 | C | T | synonymous_variant | LOW | c.1146G>A|p.Gly382Gly |
S174 S27 |
7 | BAA09g54670 | A09 | 55203857 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.883-1G>A| |
S303 |
8 | BAA09g54670 | A09 | 55204733 | C | T | stop_gained | HIGH | c.530G>A|p.Trp177* |
S206 S26 |
9 | BAA09g54670 | A09 | 55206393 | C | T | upstream_gene_variant | MODIFIER | c.-804G>A| |
S118 |
10 | BAA09g54670 | A09 | 55207807 | G | A | upstream_gene_variant | MODIFIER | c.-2218C>T| |
S36 |