Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g06440 | A10 | 3300784 | C | T | missense_variant | MODERATE | c.356G>A|p.Arg119Lys |
S10 |
2 | BAA10g06440 | A10 | 3302044 | C | T | upstream_gene_variant | MODIFIER | c.-826G>A| |
S54 |
3 | BAA10g06440 | A10 | 3302386 | G | A | upstream_gene_variant | MODIFIER | c.-1168C>T| |
S164 |
4 | BAA10g06440 | A10 | 3302755 | G | A | upstream_gene_variant | MODIFIER | c.-1537C>T| |
S252 |
5 | BAA10g06440 | A10 | 3302757 | G | A | upstream_gene_variant | MODIFIER | c.-1539C>T| |
S107 |
6 | BAA10g06440 | A10 | 3303018 | G | A | upstream_gene_variant | MODIFIER | c.-1800C>T| |
S100 |
7 | BAA10g06440 | A10 | 3304189 | C | T | upstream_gene_variant | MODIFIER | c.-2971G>A| |
S173 |
8 | BAA10g06440 | A10 | 3304329 | C | T | upstream_gene_variant | MODIFIER | c.-3111G>A| |
S28 |
9 | BAA10g06440 | A10 | 3304688 | G | A | upstream_gene_variant | MODIFIER | c.-3470C>T| |
S182 |
10 | BAA10g06440 | A10 | 3305138 | C | T | upstream_gene_variant | MODIFIER | c.-3920G>A| |
S73 S91 |
11 | BAA10g06440 | A10 | 3305190 | C | T | upstream_gene_variant | MODIFIER | c.-3972G>A| |
S15 S4 S6 |
12 | BAA10g06440 | A10 | 3305404 | C | T | upstream_gene_variant | MODIFIER | c.-4186G>A| |
S98 |