Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g08740 | A09 | 4885599 | C | T | missense_variant | MODERATE | c.17C>T|p.Ser6Phe |
S123 |
2 | BAA09g08740 | A09 | 4885623 | G | A | splice_donor_variant&intron_variant | HIGH | c.40+1G>A| |
S185 |
3 | BAA09g08740 | A09 | 4887840 | C | T | missense_variant | MODERATE | c.887C>T|p.Pro296Leu |
S257 |
4 | BAA09g08740 | A09 | 4887953 | C | T | synonymous_variant | LOW | c.1000C>T|p.Leu334Leu |
S288 |
5 | BAA09g08740 | A09 | 4890252 | G | A | missense_variant | MODERATE | c.2419G>A|p.Gly807Ser |
S195 |