Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g61330 | A09 | 58451237 | C | T | missense_variant | MODERATE | c.3034G>A|p.Glu1012Lys |
S168 |
2 | BAA09g61330 | A09 | 58452359 | G | A | missense_variant | MODERATE | c.2420C>T|p.Ser807Phe |
S126 |
3 | BAA09g61330 | A09 | 58452653 | C | T | missense_variant | MODERATE | c.2191G>A|p.Glu731Lys |
S183 S198 |
4 | BAA09g61330 | A09 | 58452665 | G | A | missense_variant | MODERATE | c.2179C>T|p.Pro727Ser |
S12 |
5 | BAA09g61330 | A09 | 58453541 | G | A | synonymous_variant | LOW | c.1303C>T|p.Leu435Leu |
S225 |
6 | BAA09g61330 | A09 | 58453952 | C | T | missense_variant | MODERATE | c.892G>A|p.Asp298Asn |
S207 |
7 | BAA09g61330 | A09 | 58454108 | G | A | missense_variant | MODERATE | c.736C>T|p.Leu246Phe |
S132 S137 S215 |
8 | BAA09g61330 | A09 | 58454378 | C | T | missense_variant | MODERATE | c.466G>A|p.Gly156Arg |
S245 |
9 | BAA09g61330 | A09 | 58454394 | G | A | synonymous_variant | LOW | c.450C>T|p.Val150Val |
S144 |
10 | BAA09g61330 | A09 | 58454656 | C | T | missense_variant | MODERATE | c.188G>A|p.Gly63Glu |
S135 |
11 | BAA09g61330 | A09 | 58455874 | C | T | upstream_gene_variant | MODIFIER | c.-1031G>A| |
S174 S27 |
12 | BAA09g61330 | A09 | 58457565 | C | T | upstream_gene_variant | MODIFIER | c.-2722G>A| |
S278 |
13 | BAA09g61330 | A09 | 58459032 | G | A | upstream_gene_variant | MODIFIER | c.-4189C>T| |
S25 |