Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g22860 | A10 | 19458307 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.619-1G>A| |
S238 |
2 | BAA10g22860 | A10 | 19458695 | C | T | missense_variant | MODERATE | c.403G>A|p.Asp135Asn |
S28 |
3 | BAA10g22860 | A10 | 19458863 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.236-1G>A| |
S266 |
4 | BAA10g22860 | A10 | 19459061 | C | T | missense_variant | MODERATE | c.130G>A|p.Gly44Ser |
S185 |
5 | BAA10g22860 | A10 | 19459780 | G | T | upstream_gene_variant | MODIFIER | c.-590C>A| |
S280 |
6 | BAA10g22860 | A10 | 19459999 | G | A | upstream_gene_variant | MODIFIER | c.-809C>T| |
S62 |
7 | BAA10g22860 | A10 | 19460496 | G | A | upstream_gene_variant | MODIFIER | c.-1306C>T| |
S88 |
8 | BAA10g22860 | A10 | 19462788 | C | T | upstream_gene_variant | MODIFIER | c.-3598G>A| |
S116 |
9 | BAA10g22860 | A10 | 19463999 | G | A | upstream_gene_variant | MODIFIER | c.-4809C>T| |
S289 S290 |