Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g01810 | A10 | 868404 | G | A | upstream_gene_variant | MODIFIER | c.-3157G>A| |
S225 S73 |
2 | BAA10g01810 | A10 | 871862 | G | A | missense_variant | MODERATE | c.206G>A|p.Gly69Glu |
S159 S243 |
3 | BAA10g01810 | A10 | 872020 | C | T | missense_variant | MODERATE | c.364C>T|p.Arg122Cys |
S11 S56 |
4 | BAA10g01810 | A10 | 872260 | G | A | synonymous_variant | LOW | c.492G>A|p.Leu164Leu |
S1 S90 |
5 | BAA10g01810 | A10 | 873128 | G | A | missense_variant | MODERATE | c.997G>A|p.Ala333Thr |
S237 |
6 | BAA10g01810 | A10 | 873602 | C | T | synonymous_variant | LOW | c.1293C>T|p.Val431Val |
S244 |
7 | BAA10g01810 | A10 | 873642 | G | A | missense_variant | MODERATE | c.1333G>A|p.Glu445Lys |
S153 S213 |
8 | BAA10g01810 | A10 | 876941 | C | T | downstream_gene_variant | MODIFIER | c.*2882C>T| |
S42 |
9 | BAA10g01810 | A10 | 877032 | G | A | downstream_gene_variant | MODIFIER | c.*2973G>A| |
S38 |
10 | BAA10g01810 | A10 | 877079 | G | A | downstream_gene_variant | MODIFIER | c.*3020G>A| |
S274 |
11 | BAA10g01810 | A10 | 877518 | G | A | downstream_gene_variant | MODIFIER | c.*3459G>A| |
S252 |
12 | BAA10g01810 | A10 | 877762 | G | A | downstream_gene_variant | MODIFIER | c.*3703G>A| |
S295 |
13 | BAA10g01810 | A10 | 877935 | C | T | downstream_gene_variant | MODIFIER | c.*3876C>T| |
S166 |
14 | BAA10g01810 | A10 | 878364 | G | A | downstream_gene_variant | MODIFIER | c.*4305G>A| |
S245 |
15 | BAA10g01810 | A10 | 878392 | C | T | downstream_gene_variant | MODIFIER | c.*4333C>T| |
S117 |