Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g53160 | A09 | 54534033 | G | A | missense_variant | MODERATE | c.1892C>T|p.Ala631Val |
S247 |
2 | BAA09g53160 | A09 | 54534187 | C | T | missense_variant&splice_region_variant | MODERATE | c.1738G>A|p.Val580Ile |
S67 |
3 | BAA09g53160 | A09 | 54535119 | C | T | missense_variant | MODERATE | c.1132G>A|p.Glu378Lys |
S179 |
4 | BAA09g53160 | A09 | 54535404 | C | T | synonymous_variant | LOW | c.1047G>A|p.Lys349Lys |
S117 |
5 | BAA09g53160 | A09 | 54536193 | G | A | missense_variant | MODERATE | c.623C>T|p.Ser208Phe |
S268 |
6 | BAA09g53160 | A09 | 54537122 | C | T | missense_variant | MODERATE | c.311G>A|p.Arg104Lys |
S162 |
7 | BAA09g53160 | A09 | 54537928 | G | A | upstream_gene_variant | MODIFIER | c.-384C>T| |
S23 |
8 | BAA09g53160 | A09 | 54537934 | G | A | upstream_gene_variant | MODIFIER | c.-390C>T| |
S158 |
9 | BAA09g53160 | A09 | 54540784 | C | T | upstream_gene_variant | MODIFIER | c.-3240G>A| |
S168 |
10 | BAA09g53160 | A09 | 54541065 | C | G | upstream_gene_variant | MODIFIER | c.-3521G>C| |
S155 S211 |