Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g26050 | A10 | 20785033 | C | T | splice_region_variant&intron_variant | LOW | c.1497+8G>A| |
S136 S301 S304 |
2 | BAA10g26050 | A10 | 20786365 | C | T | missense_variant | MODERATE | c.739G>A|p.Asp247Asn |
S305 |
3 | BAA10g26050 | A10 | 20790884 | G | A | upstream_gene_variant | MODIFIER | c.-3163C>T| |
S9 |