Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g16900 | A10 | 16513728 | C | T | missense_variant | MODERATE | c.967G>A|p.Val323Ile |
S163 |
2 | BAA10g16900 | A10 | 16513737 | C | T | missense_variant&splice_region_variant | MODERATE | c.958G>A|p.Gly320Ser |
S163 |
3 | BAA10g16900 | A10 | 16514097 | C | T | missense_variant | MODERATE | c.676G>A|p.Val226Ile |
S162 |
4 | BAA10g16900 | A10 | 16516398 | G | A | upstream_gene_variant | MODIFIER | c.-959C>T| |
S27 |
5 | BAA10g16900 | A10 | 16516684 | G | A | upstream_gene_variant | MODIFIER | c.-1245C>T| |
S295 |
6 | BAA10g16900 | A10 | 16519821 | C | T | upstream_gene_variant | MODIFIER | c.-4382G>A| |
S42 |