Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g05930 | A10 | 3038876 | G | A | upstream_gene_variant | MODIFIER | c.-1744G>A| |
S83 S88 |
2 | BAA10g05930 | A10 | 3038940 | C | T | upstream_gene_variant | MODIFIER | c.-1680C>T| |
S291 S42 |
3 | BAA10g05930 | A10 | 3039716 | G | A | upstream_gene_variant | MODIFIER | c.-904G>A| |
S184 |
4 | BAA10g05930 | A10 | 3040337 | G | A | upstream_gene_variant | MODIFIER | c.-283G>A| |
S92 |
5 | BAA10g05930 | A10 | 3040925 | A | T | synonymous_variant | LOW | c.306A>T|p.Ile102Ile |
S279 |
6 | BAA10g05930 | A10 | 3041695 | C | T | synonymous_variant | LOW | c.612C>T|p.Ile204Ile |
S73 S91 |
7 | BAA10g05930 | A10 | 3041907 | G | A | missense_variant | MODERATE | c.824G>A|p.Ser275Asn |
S261 |
8 | BAA10g05930 | A10 | 3042006 | C | T | intron_variant | MODIFIER | c.897+26C>T| |
S49 |
9 | BAA10g05930 | A10 | 3042012 | C | T | intron_variant | MODIFIER | c.897+32C>T| |
S19 |
10 | BAA10g05930 | A10 | 3043380 | G | A | downstream_gene_variant | MODIFIER | c.*656G>A| |
S207 |
11 | BAA10g05930 | A10 | 3043529 | G | A | downstream_gene_variant | MODIFIER | c.*805G>A| |
S133 |
12 | BAA10g05930 | A10 | 3044739 | C | T | downstream_gene_variant | MODIFIER | c.*2015C>T| |
S189 |
13 | BAA10g05930 | A10 | 3045638 | G | A | downstream_gene_variant | MODIFIER | c.*2914G>A| |
S90 |
14 | BAA10g05930 | A10 | 3046242 | G | A | downstream_gene_variant | MODIFIER | c.*3518G>A| |
S240 |
15 | BAA10g05930 | A10 | 3046402 | C | T | downstream_gene_variant | MODIFIER | c.*3678C>T| |
S233 |
16 | BAA10g05930 | A10 | 3047502 | C | T | downstream_gene_variant | MODIFIER | c.*4778C>T| |
S95 |