Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g66630 | A09 | 60797843 | C | T | missense_variant | MODERATE | c.2320G>A|p.Glu774Lys |
S259 |
2 | BAA09g66630 | A09 | 60798020 | C | T | missense_variant | MODERATE | c.2143G>A|p.Glu715Lys |
S138 |
3 | BAA09g66630 | A09 | 60798595 | C | T | missense_variant | MODERATE | c.1568G>A|p.Gly523Glu |
S51 |
4 | BAA09g66630 | A09 | 60798794 | C | T | missense_variant | MODERATE | c.1369G>A|p.Glu457Lys |
S249 |
5 | BAA09g66630 | A09 | 60799043 | C | T | missense_variant | MODERATE | c.1120G>A|p.Asp374Asn |
S183 S198 |
6 | BAA09g66630 | A09 | 60799193 | G | A | missense_variant | MODERATE | c.970C>T|p.Leu324Phe |
S79 S84 |
7 | BAA09g66630 | A09 | 60799318 | G | A | missense_variant | MODERATE | c.845C>T|p.Pro282Leu |
S291 |
8 | BAA09g66630 | A09 | 60799409 | C | T | missense_variant | MODERATE | c.754G>A|p.Asp252Asn |
S198 |
9 | BAA09g66630 | A09 | 60800156 | C | T | missense_variant | MODERATE | c.596G>A|p.Gly199Glu |
S198 |
10 | BAA09g66630 | A09 | 60800312 | C | T | missense_variant | MODERATE | c.440G>A|p.Gly147Glu |
S107 |
11 | BAA09g66630 | A09 | 60800837 | G | A | missense_variant | MODERATE | c.37C>T|p.Arg13Cys |
S265 |
12 | BAA09g66630 | A09 | 60802714 | C | T | upstream_gene_variant | MODIFIER | c.-1841G>A| |
S305 |
13 | BAA09g66630 | A09 | 60804565 | C | T | upstream_gene_variant | MODIFIER | c.-3692G>A| |
S152 |
14 | BAA09g66630 | A09 | 60805143 | G | A | upstream_gene_variant | MODIFIER | c.-4270C>T| |
S255 |