Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g09910 | A10 | 11736386 | C | T | upstream_gene_variant | MODIFIER | c.-4193C>T| |
S149 |
2 | BAA10g09910 | A10 | 11737418 | G | A | upstream_gene_variant | MODIFIER | c.-3161G>A| |
S178 |
3 | BAA10g09910 | A10 | 11737593 | G | A | upstream_gene_variant | MODIFIER | c.-2986G>A| |
S229 |
4 | BAA10g09910 | A10 | 11737967 | C | T | upstream_gene_variant | MODIFIER | c.-2612C>T| |
S111 S143 |
5 | BAA10g09910 | A10 | 11738290 | G | A | upstream_gene_variant | MODIFIER | c.-2289G>A| |
S234 |
6 | BAA10g09910 | A10 | 11738402 | C | T | upstream_gene_variant | MODIFIER | c.-2177C>T| |
S187 |
7 | BAA10g09910 | A10 | 11738745 | C | T | upstream_gene_variant | MODIFIER | c.-1834C>T| |
S282 |
8 | BAA10g09910 | A10 | 11738896 | C | T | upstream_gene_variant | MODIFIER | c.-1683C>T| |
S167 |
9 | BAA10g09910 | A10 | 11739025 | C | T | upstream_gene_variant | MODIFIER | c.-1554C>T| |
S235 S269 |
10 | BAA10g09910 | A10 | 11740707 | T | A | missense_variant | MODERATE | c.129T>A|p.Asp43Glu |
S7 |
11 | BAA10g09910 | A10 | 11740727 | G | A | missense_variant | MODERATE | c.149G>A|p.Arg50Gln |
S157 S163 |
12 | BAA10g09910 | A10 | 11745709 | G | A | downstream_gene_variant | MODIFIER | c.*4039G>A| |
S148 S210 S30 S31 |
13 | BAA10g09910 | A10 | 11745853 | C | T | downstream_gene_variant | MODIFIER | c.*4183C>T| |
S84 S93 |
14 | BAA10g09910 | A10 | 11745870 | C | T | downstream_gene_variant | MODIFIER | c.*4200C>T| |
S92 |
15 | BAA10g09910 | A10 | 11746482 | G | A | downstream_gene_variant | MODIFIER | c.*4812G>A| |
S69 |