Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g22510 | A10 | 19302835 | C | T | missense_variant | MODERATE | c.1345G>A|p.Ala449Thr |
S34 |
2 | BAA10g22510 | A10 | 19303188 | G | A | missense_variant | MODERATE | c.992C>T|p.Ser331Leu |
S61 |
3 | BAA10g22510 | A10 | 19303266 | G | A | missense_variant | MODERATE | c.914C>T|p.Thr305Ile |
S18 |
4 | BAA10g22510 | A10 | 19303594 | C | T | missense_variant | MODERATE | c.586G>A|p.Asp196Asn |
S150 |
5 | BAA10g22510 | A10 | 19303781 | G | A | synonymous_variant | LOW | c.399C>T|p.Leu133Leu |
S191 |
6 | BAA10g22510 | A10 | 19303856 | G | A | synonymous_variant | LOW | c.324C>T|p.Phe108Phe |
S219 S72 |
7 | BAA10g22510 | A10 | 19303878 | C | T | missense_variant | MODERATE | c.302G>A|p.Gly101Asp |
S275 |
8 | BAA10g22510 | A10 | 19308991 | G | A | upstream_gene_variant | MODIFIER | c.-4812C>T| |
S117 |
9 | BAA10g22510 | A10 | 19309102 | G | A | upstream_gene_variant | MODIFIER | c.-4923C>T| |
S149 |