Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g11660 | A07 | 20340962 | C | T | missense_variant | MODERATE | c.25C>T|p.Leu9Phe |
S261 |
2 | BAA07g11660 | A07 | 20341732 | C | T | missense_variant | MODERATE | c.320C>T|p.Pro107Leu |
S32 |
3 | BAA07g11660 | A07 | 20342124 | G | A | splice_donor_variant&intron_variant | HIGH | c.621+1G>A| |
S157 S163 |
4 | BAA07g11660 | A07 | 20344066 | C | T | synonymous_variant | LOW | c.1282C>T|p.Leu428Leu |
S143 |
5 | BAA07g11660 | A07 | 20344701 | G | A | synonymous_variant | LOW | c.1584G>A|p.Glu528Glu |
S123 |