Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g00250 | A10 | 117768 | C | T | upstream_gene_variant | MODIFIER | c.-1172C>T| |
S185 |
2 | BAA10g00250 | A10 | 118361 | C | T | upstream_gene_variant | MODIFIER | c.-579C>T| |
S35 |
3 | BAA10g00250 | A10 | 118584 | C | T | upstream_gene_variant | MODIFIER | c.-356C>T| |
S293 |
4 | BAA10g00250 | A10 | 119015 | C | T | missense_variant | MODERATE | c.76C>T|p.Pro26Ser |
S287 |
5 | BAA10g00250 | A10 | 119668 | G | A | synonymous_variant | LOW | c.501G>A|p.Thr167Thr |
S194 |
6 | BAA10g00250 | A10 | 120089 | C | T | missense_variant | MODERATE | c.773C>T|p.Ser258Phe |
S134 |
7 | BAA10g00250 | A10 | 120244 | C | T | synonymous_variant | LOW | c.862C>T|p.Leu288Leu |
S201 |
8 | BAA10g00250 | A10 | 120483 | C | T | missense_variant | MODERATE | c.1007C>T|p.Thr336Ile |
S11 |