Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g35120 | A08 | 22414183 | G | A | missense_variant | MODERATE | c.4G>A|p.Gly2Arg |
S36 |
2 | BAA08g35120 | A08 | 22415412 | G | A | missense_variant | MODERATE | c.616G>A|p.Asp206Asn |
S291 |
3 | BAA08g35120 | A08 | 22415840 | C | T | missense_variant | MODERATE | c.878C>T|p.Ser293Phe |
S286 |
4 | BAA08g35120 | A08 | 22416089 | G | A | missense_variant | MODERATE | c.1057G>A|p.Gly353Arg |
S8 |
5 | BAA08g35120 | A08 | 22416439 | C | T | missense_variant | MODERATE | c.1336C>T|p.Pro446Ser |
S134 |
6 | BAA08g35120 | A08 | 22417316 | G | A | missense_variant | MODERATE | c.1850G>A|p.Arg617Lys |
S211 S227 |
7 | BAA08g35120 | A08 | 22418535 | C | T | missense_variant | MODERATE | c.2563C>T|p.Pro855Ser |
S125 |
8 | BAA08g35120 | A08 | 22418559 | G | A | missense_variant | MODERATE | c.2587G>A|p.Val863Ile |
S204 |
9 | BAA08g35120 | A08 | 22419000 | C | T | downstream_gene_variant | MODIFIER | c.*177C>T| |
S295 |