Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g15000 | A09 | 8576742 | C | T | missense_variant | MODERATE | c.3175G>A|p.Asp1059Asn |
S69 |
2 | BAA09g15000 | A09 | 8577356 | G | A | missense_variant | MODERATE | c.2777C>T|p.Ser926Phe |
S12 |
3 | BAA09g15000 | A09 | 8577875 | G | A | missense_variant | MODERATE | c.2258C>T|p.Pro753Leu |
S184 |
4 | BAA09g15000 | A09 | 8578130 | G | A | missense_variant | MODERATE | c.2003C>T|p.Pro668Leu |
S273 |
5 | BAA09g15000 | A09 | 8578399 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.1735-1G>A| |
S8 |
6 | BAA09g15000 | A09 | 8579594 | C | T | missense_variant | MODERATE | c.1228G>A|p.Ala410Thr |
S177 |
7 | BAA09g15000 | A09 | 8580312 | C | T | missense_variant | MODERATE | c.590G>A|p.Arg197His |
S80 |
8 | BAA09g15000 | A09 | 8581344 | G | A | upstream_gene_variant | MODIFIER | c.-443C>T| |
S182 |