Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g29300 | A08 | 20159623 | C | T | synonymous_variant | LOW | c.1665G>A|p.Lys555Lys |
S13 |
2 | BAA08g29300 | A08 | 20159787 | G | A | missense_variant | MODERATE | c.1501C>T|p.His501Tyr |
S287 |
3 | BAA08g29300 | A08 | 20165954 | C | T | missense_variant | MODERATE | c.595G>A|p.Glu199Lys |
S53 |
4 | BAA08g29300 | A08 | 20166015 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.535-1G>A| |
S149 |
5 | BAA08g29300 | A08 | 20167556 | G | A | missense_variant | MODERATE | c.191C>T|p.Pro64Leu |
S65 |
6 | BAA08g29300 | A08 | 20169307 | C | T | upstream_gene_variant | MODIFIER | c.-727G>A| |
S181 |
7 | BAA08g29300 | A08 | 20172634 | C | T | upstream_gene_variant | MODIFIER | c.-4054G>A| |
S94 |
8 | BAA08g29300 | A08 | 20173001 | C | T | upstream_gene_variant | MODIFIER | c.-4421G>A| |
S231 |
9 | BAA08g29300 | A08 | 20173028 | C | T | upstream_gene_variant | MODIFIER | c.-4448G>A| |
S41 |