Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g17880 | A09 | 10743250 | C | T | upstream_gene_variant | MODIFIER | c.-836C>T| |
S9 |
2 | BAA09g17880 | A09 | 10743379 | A | T | upstream_gene_variant | MODIFIER | c.-707A>T| |
S298 |
3 | BAA09g17880 | A09 | 10744650 | G | A | missense_variant | MODERATE | c.235G>A|p.Glu79Lys |
S181 |
4 | BAA09g17880 | A09 | 10744767 | G | A | missense_variant | MODERATE | c.352G>A|p.Glu118Lys |
S198 |
5 | BAA09g17880 | A09 | 10744798 | C | T | missense_variant | MODERATE | c.383C>T|p.Ser128Phe |
S212 |
6 | BAA09g17880 | A09 | 10744950 | G | A | missense_variant | MODERATE | c.535G>A|p.Gly179Arg |
S207 |
7 | BAA09g17880 | A09 | 10744961 | G | A | synonymous_variant | LOW | c.546G>A|p.Gln182Gln |
S164 |
8 | BAA09g17880 | A09 | 10744972 | C | T | missense_variant | MODERATE | c.557C>T|p.Ala186Val |
S230 |
9 | BAA09g17880 | A09 | 10745219 | G | A | synonymous_variant | LOW | c.804G>A|p.Gln268Gln |
S277 |