Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g19660 | A04 | 23073366 | G | A | missense_variant | MODERATE | c.2167C>T|p.Pro723Ser |
S17 |
2 | BAA04g19660 | A04 | 23073873 | C | T | missense_variant | MODERATE | c.1660G>A|p.Ala554Thr |
S197 S31 |
3 | BAA04g19660 | A04 | 23073945 | C | T | missense_variant | MODERATE | c.1588G>A|p.Glu530Lys |
S260 |
4 | BAA04g19660 | A04 | 23074011 | C | T | missense_variant | MODERATE | c.1522G>A|p.Glu508Lys |
S284 |
5 | BAA04g19660 | A04 | 23074833 | C | T | missense_variant | MODERATE | c.700G>A|p.Glu234Lys |
S50 |
6 | BAA04g19660 | A04 | 23075037 | C | T | missense_variant | MODERATE | c.496G>A|p.Glu166Lys |
S123 |
7 | BAA04g19660 | A04 | 23075080 | C | T | stop_gained | HIGH | c.453G>A|p.Trp151* |
S296 |
8 | BAA04g19660 | A04 | 23075251 | C | T | synonymous_variant | LOW | c.282G>A|p.Glu94Glu |
S178 |
9 | BAA04g19660 | A04 | 23075327 | G | A | missense_variant | MODERATE | c.206C>T|p.Ser69Phe |
S105 S106 |
10 | BAA04g19660 | A04 | 23076162 | C | T | upstream_gene_variant | MODIFIER | c.-630G>A| |
S279 |
11 | BAA04g19660 | A04 | 23078213 | C | T | upstream_gene_variant | MODIFIER | c.-2681G>A| |
S188 |