Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g13670 | A01 | 6499754 | C | T | upstream_gene_variant | MODIFIER | c.-3109C>T| |
S144 |
2 | BAA01g13670 | A01 | 6503086 | C | T | missense_variant | MODERATE | c.224C>T|p.Ser75Phe |
S69 |
3 | BAA01g13670 | A01 | 6503437 | C | T | missense_variant | MODERATE | c.575C>T|p.Thr192Met |
S176 |
4 | BAA01g13670 | A01 | 6506810 | G | A | missense_variant | MODERATE | c.2416G>A|p.Val806Ile |
S259 |
5 | BAA01g13670 | A01 | 6507162 | G | A | missense_variant | MODERATE | c.2687G>A|p.Gly896Glu |
S165 |
6 | BAA01g13670 | A01 | 6507427 | G | A | stop_gained | HIGH | c.2766G>A|p.Trp922* |
S191 |
7 | BAA01g13670 | A01 | 6507864 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.2926-1G>A| |
S56 |
8 | BAA01g13670 | A01 | 6508568 | C | T | missense_variant | MODERATE | c.3458C>T|p.Ser1153Phe |
S89 |
9 | BAA01g13670 | A01 | 6509164 | C | T | synonymous_variant | LOW | c.3894C>T|p.Asn1298Asn |
S153 |