Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g13770 | A10 | 14729749 | C | T | upstream_gene_variant | MODIFIER | c.-4194C>T| |
S153 S213 |
2 | BAA10g13770 | A10 | 14730288 | G | A | upstream_gene_variant | MODIFIER | c.-3655G>A| |
S136 |
3 | BAA10g13770 | A10 | 14731982 | G | A | upstream_gene_variant | MODIFIER | c.-1961G>A| |
S17 |
4 | BAA10g13770 | A10 | 14733779 | G | A | upstream_gene_variant | MODIFIER | c.-164G>A| |
S38 |
5 | BAA10g13770 | A10 | 14733869 | C | T | upstream_gene_variant | MODIFIER | c.-74C>T| |
S28 |
6 | BAA10g13770 | A10 | 14734262 | G | A | synonymous_variant | LOW | c.240G>A|p.Glu80Glu |
S61 |
7 | BAA10g13770 | A10 | 14734292 | C | T | synonymous_variant | LOW | c.270C>T|p.Pro90Pro |
S185 |
8 | BAA10g13770 | A10 | 14734979 | C | T | missense_variant | MODERATE | c.773C>T|p.Ala258Val |
S167 |
9 | BAA10g13770 | A10 | 14734993 | C | T | missense_variant | MODERATE | c.787C>T|p.Leu263Phe |
S298 |
10 | BAA10g13770 | A10 | 14739083 | C | T | downstream_gene_variant | MODIFIER | c.*3266C>T| |
S297 |
11 | BAA10g13770 | A10 | 14739259 | C | T | downstream_gene_variant | MODIFIER | c.*3442C>T| |
S204 |
12 | BAA10g13770 | A10 | 14740431 | G | A | downstream_gene_variant | MODIFIER | c.*4614G>A| |
S292 |
13 | BAA10g13770 | A10 | 14740599 | G | A | downstream_gene_variant | MODIFIER | c.*4782G>A| |
S69 |