Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g14100 | A10 | 14950340 | G | A | missense_variant | MODERATE | c.1081C>T|p.Pro361Ser |
S279 |
2 | BAA10g14100 | A10 | 14951235 | G | A | missense_variant | MODERATE | c.262C>T|p.Pro88Ser |
S127 |
3 | BAA10g14100 | A10 | 14952598 | C | T | upstream_gene_variant | MODIFIER | c.-209G>A| |
S28 |
4 | BAA10g14100 | A10 | 14952600 | G | C | upstream_gene_variant | MODIFIER | c.-211C>G| |
S28 |
5 | BAA10g14100 | A10 | 14953123 | C | T | upstream_gene_variant | MODIFIER | c.-734G>A| |
S113 |
6 | BAA10g14100 | A10 | 14955506 | G | A | upstream_gene_variant | MODIFIER | c.-3117C>T| |
S219 S72 |
7 | BAA10g14100 | A10 | 14956261 | C | T | upstream_gene_variant | MODIFIER | c.-3872G>A| |
S200 |