Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g24080 | A08 | 17684671 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.1074-1G>A| |
S232 |
2 | BAA08g24080 | A08 | 17685475 | G | A | missense_variant | MODERATE | c.1600G>A|p.Asp534Asn |
S110 S183 S198 |
3 | BAA08g24080 | A08 | 17685910 | C | T | missense_variant | MODERATE | c.1876C>T|p.Leu626Phe |
S201 |
4 | BAA08g24080 | A08 | 17685925 | C | T | missense_variant | MODERATE | c.1891C>T|p.Leu631Phe |
S69 |
5 | BAA08g24080 | A08 | 17686713 | C | T | synonymous_variant | LOW | c.2412C>T|p.Ile804Ile |
S59 |
6 | BAA08g24080 | A08 | 17686906 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.2529-1G>A| |
S87 |
7 | BAA08g24080 | A08 | 17687193 | G | A | missense_variant | MODERATE | c.2735G>A|p.Arg912Lys |
S158 |
8 | BAA08g24080 | A08 | 17687454 | C | T | missense_variant | MODERATE | c.2996C>T|p.Ser999Phe |
S301 S304 |