Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g49420 | A09 | 52766096 | G | A | missense_variant | MODERATE | c.124G>A|p.Asp42Asn |
S207 |
2 | BAA09g49420 | A09 | 52766439 | C | T | splice_region_variant&intron_variant | LOW | c.298-3C>T| |
S182 |
3 | BAA09g49420 | A09 | 52766843 | C | T | missense_variant | MODERATE | c.602C>T|p.Ala201Val |
S117 |
4 | BAA09g49420 | A09 | 52767070 | C | T | missense_variant | MODERATE | c.829C>T|p.Arg277Cys |
S192 |
5 | BAA09g49420 | A09 | 52767244 | C | T | missense_variant | MODERATE | c.1003C>T|p.Leu335Phe |
S223 |