Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g42900 | A06 | 27674033 | G | A | missense_variant | MODERATE | c.2267C>T|p.Ser756Phe |
S191 |
2 | BAA06g42900 | A06 | 27674138 | C | T | missense_variant | MODERATE | c.2162G>A|p.Gly721Glu |
S286 |
3 | BAA06g42900 | A06 | 27674407 | G | A | synonymous_variant | LOW | c.1893C>T|p.Pro631Pro |
S75 S81 |
4 | BAA06g42900 | A06 | 27674461 | G | A | synonymous_variant | LOW | c.1839C>T|p.Phe613Phe |
S177 |
5 | BAA06g42900 | A06 | 27675531 | C | T | missense_variant | MODERATE | c.1438G>A|p.Asp480Asn |
S57 |
6 | BAA06g42900 | A06 | 27676333 | C | T | stop_gained | HIGH | c.636G>A|p.Trp212* |
S278 |
7 | BAA06g42900 | A06 | 27680309 | C | T | upstream_gene_variant | MODIFIER | c.-3341G>A| |
S252 |
8 | BAA06g42900 | A06 | 27681559 | A | G | upstream_gene_variant | MODIFIER | c.-4591T>C| |
S203 |
9 | BAA06g42900 | A06 | 27681865 | G | A | upstream_gene_variant | MODIFIER | c.-4897C>T| |
S201 |