Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g21070 | A10 | 18664248 | C | T | upstream_gene_variant | MODIFIER | c.-2542C>T| |
S162 |
2 | BAA10g21070 | A10 | 18667733 | G | A | missense_variant | MODERATE | c.272G>A|p.Arg91Lys |
S192 |
3 | BAA10g21070 | A10 | 18667965 | C | T | synonymous_variant | LOW | c.405C>T|p.Cys135Cys |
S107 |
4 | BAA10g21070 | A10 | 18668355 | A | C | synonymous_variant | LOW | c.708A>C|p.Ile236Ile |
S157 S163 S249 S43 |
5 | BAA10g21070 | A10 | 18668462 | G | A | missense_variant | MODERATE | c.815G>A|p.Gly272Glu |
S69 |
6 | BAA10g21070 | A10 | 18668770 | G | A | missense_variant | MODERATE | c.1123G>A|p.Ala375Thr |
S27 |
7 | BAA10g21070 | A10 | 18668993 | G | A | missense_variant | MODERATE | c.1346G>A|p.Gly449Glu |
S270 |
8 | BAA10g21070 | A10 | 18669485 | G | A | missense_variant | MODERATE | c.1838G>A|p.Arg613Lys |
S279 |
9 | BAA10g21070 | A10 | 18670806 | G | A | splice_donor_variant&intron_variant | HIGH | c.2793+1G>A| |
S288 |