Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g00700 | A08 | 523314 | C | T | missense_variant | MODERATE | c.98C>T|p.Ser33Phe |
S305 |
2 | BAA08g00700 | A08 | 523630 | C | T | synonymous_variant | LOW | c.192C>T|p.Ile64Ile |
S177 |
3 | BAA08g00700 | A08 | 524147 | G | A | missense_variant | MODERATE | c.548G>A|p.Gly183Glu |
S278 |
4 | BAA08g00700 | A08 | 524260 | G | A | missense_variant | MODERATE | c.661G>A|p.Asp221Asn |
S192 |
5 | BAA08g00700 | A08 | 524562 | C | T | stop_gained | HIGH | c.799C>T|p.Gln267* |
S276 |
6 | BAA08g00700 | A08 | 524721 | C | T | intron_variant | MODIFIER | c.892-15C>T| |
S189 |