Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g01790 | A10 | 848990 | C | T | upstream_gene_variant | MODIFIER | c.-3430C>T| |
S260 |
2 | BAA10g01790 | A10 | 852585 | G | A | missense_variant | MODERATE | c.166G>A|p.Glu56Lys |
S85 |
3 | BAA10g01790 | A10 | 852823 | G | A | stop_gained | HIGH | c.404G>A|p.Trp135* |
S157 S163 |
4 | BAA10g01790 | A10 | 852864 | G | A | missense_variant | MODERATE | c.445G>A|p.Asp149Asn |
S19 |
5 | BAA10g01790 | A10 | 854280 | C | T | missense_variant | MODERATE | c.1405C>T|p.Leu469Phe |
S265 |
6 | BAA10g01790 | A10 | 854350 | G | A | missense_variant | MODERATE | c.1475G>A|p.Gly492Glu |
S261 |
7 | BAA10g01790 | A10 | 855537 | G | A | downstream_gene_variant | MODIFIER | c.*804G>A| |
S19 |