Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g10920 | A10 | 12651280 | C | T | missense_variant&splice_region_variant | MODERATE | c.1168C>T|p.Leu390Phe |
S73 S91 |
2 | BAA10g10920 | A10 | 12651443 | G | A | missense_variant | MODERATE | c.1331G>A|p.Arg444Gln |
S184 |
3 | BAA10g10920 | A10 | 12653261 | C | T | downstream_gene_variant | MODIFIER | c.*1751C>T| |
S190 |
4 | BAA10g10920 | A10 | 12655130 | G | A | downstream_gene_variant | MODIFIER | c.*3620G>A| |
S288 |
5 | BAA10g10920 | A10 | 12655363 | C | T | downstream_gene_variant | MODIFIER | c.*3853C>T| |
S38 |