Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g49480 | A09 | 52778527 | G | A | missense_variant | MODERATE | c.1231C>T|p.Pro411Ser |
S189 |
2 | BAA09g49480 | A09 | 52778662 | C | T | missense_variant | MODERATE | c.1096G>A|p.Gly366Arg |
S301 S304 |
3 | BAA09g49480 | A09 | 52778737 | C | T | missense_variant | MODERATE | c.1021G>A|p.Ala341Thr |
S296 |
4 | BAA09g49480 | A09 | 52779034 | C | T | missense_variant | MODERATE | c.724G>A|p.Ala242Thr |
S278 |
5 | BAA09g49480 | A09 | 52779141 | G | A | missense_variant | MODERATE | c.617C>T|p.Ala206Val |
S177 |
6 | BAA09g49480 | A09 | 52779162 | C | T | missense_variant | MODERATE | c.596G>A|p.Gly199Glu |
S279 |
7 | BAA09g49480 | A09 | 52779268 | G | A | synonymous_variant | LOW | c.490C>T|p.Leu164Leu |
S240 |