Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g45630 | A09 | 50779811 | C | T | missense_variant | MODERATE | c.934G>A|p.Asp312Asn |
S117 |
2 | BAA09g45630 | A09 | 50779837 | C | T | missense_variant | MODERATE | c.908G>A|p.Arg303Lys |
S184 |
3 | BAA09g45630 | A09 | 50779907 | C | T | missense_variant | MODERATE | c.838G>A|p.Gly280Arg |
S267 |
4 | BAA09g45630 | A09 | 50780501 | C | T | missense_variant | MODERATE | c.244G>A|p.Asp82Asn |
S40 S49 |
5 | BAA09g45630 | A09 | 50782688 | G | A | upstream_gene_variant | MODIFIER | c.-1872C>T| |
S36 |
6 | BAA09g45630 | A09 | 50782931 | G | A | upstream_gene_variant | MODIFIER | c.-2115C>T| |
S177 |
7 | BAA09g45630 | A09 | 50783242 | C | T | upstream_gene_variant | MODIFIER | c.-2426G>A| |
S282 |
8 | BAA09g45630 | A09 | 50784069 | C | T | upstream_gene_variant | MODIFIER | c.-3253G>A| |
S242 |
9 | BAA09g45630 | A09 | 50784375 | G | A | upstream_gene_variant | MODIFIER | c.-3559C>T| |
S135 |
10 | BAA09g45630 | A09 | 50784508 | G | A | upstream_gene_variant | MODIFIER | c.-3692C>T| |
S244 |
11 | BAA09g45630 | A09 | 50785211 | C | T | upstream_gene_variant | MODIFIER | c.-4395G>A| |
S132 S137 S138 S215 S288 |
12 | BAA09g45630 | A09 | 50785272 | C | T | upstream_gene_variant | MODIFIER | c.-4456G>A| |
S66 |