Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g09090 | A10 | 11163604 | G | A | upstream_gene_variant | MODIFIER | c.-2274G>A| |
S43 |
2 | BAA10g09090 | A10 | 11163623 | C | T | upstream_gene_variant | MODIFIER | c.-2255C>T| |
S92 |
3 | BAA10g09090 | A10 | 11163835 | G | A | upstream_gene_variant | MODIFIER | c.-2043G>A| |
S192 |
4 | BAA10g09090 | A10 | 11164456 | A | G | upstream_gene_variant | MODIFIER | c.-1422A>G| |
S252 |
5 | BAA10g09090 | A10 | 11164818 | G | A | upstream_gene_variant | MODIFIER | c.-1060G>A| |
S198 |
6 | BAA10g09090 | A10 | 11165058 | G | A | upstream_gene_variant | MODIFIER | c.-820G>A| |
S134 |
7 | BAA10g09090 | A10 | 11165124 | C | T | upstream_gene_variant | MODIFIER | c.-754C>T| |
S170 |
8 | BAA10g09090 | A10 | 11165157 | G | A | upstream_gene_variant | MODIFIER | c.-721G>A| |
S127 |
9 | BAA10g09090 | A10 | 11165212 | C | T | upstream_gene_variant | MODIFIER | c.-666C>T| |
S70 |
10 | BAA10g09090 | A10 | 11165980 | G | A | missense_variant | MODERATE | c.103G>A|p.Val35Ile |
S45 |
11 | BAA10g09090 | A10 | 11166327 | G | A | missense_variant | MODERATE | c.238G>A|p.Glu80Lys |
S219 S72 |
12 | BAA10g09090 | A10 | 11166962 | G | A | synonymous_variant | LOW | c.873G>A|p.Gln291Gln |
S179 |