Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g19710 | A10 | 18000531 | C | T | missense_variant | MODERATE | c.379G>A|p.Glu127Lys |
S308 |
2 | BAA10g19710 | A10 | 18000582 | C | T | missense_variant | MODERATE | c.328G>A|p.Ala110Thr |
S109 S26 |
3 | BAA10g19710 | A10 | 18001263 | C | T | upstream_gene_variant | MODIFIER | c.-354G>A| |
S117 |
4 | BAA10g19710 | A10 | 18003385 | G | A | upstream_gene_variant | MODIFIER | c.-2476C>T| |
S303 |
5 | BAA10g19710 | A10 | 18004452 | G | A | upstream_gene_variant | MODIFIER | c.-3543C>T| |
S57 |
6 | BAA10g19710 | A10 | 18005048 | G | A | upstream_gene_variant | MODIFIER | c.-4139C>T| |
S175 |
7 | BAA10g19710 | A10 | 18005200 | G | A | upstream_gene_variant | MODIFIER | c.-4291C>T| |
S25 |
8 | BAA10g19710 | A10 | 18005734 | C | T | upstream_gene_variant | MODIFIER | c.-4825G>A| |
S143 |