Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g17790 | A10 | 16963993 | C | T | upstream_gene_variant | MODIFIER | c.-4453C>T| |
S238 |
2 | BAA10g17790 | A10 | 16968610 | C | T | synonymous_variant | LOW | c.165C>T|p.Asn55Asn |
S87 |
3 | BAA10g17790 | A10 | 16968665 | G | A | missense_variant | MODERATE | c.220G>A|p.Asp74Asn |
S212 |
4 | BAA10g17790 | A10 | 16968847 | G | A | synonymous_variant | LOW | c.402G>A|p.Lys134Lys |
S112 |
5 | BAA10g17790 | A10 | 16974407 | C | T | downstream_gene_variant | MODIFIER | c.*4960C>T| |
S10 |