Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g01970 | A10 | 939796 | G | T | upstream_gene_variant | MODIFIER | c.-3519G>T| |
S158 S160 |
2 | BAA10g01970 | A10 | 939845 | G | A | upstream_gene_variant | MODIFIER | c.-3470G>A| |
S198 |
3 | BAA10g01970 | A10 | 943077 | G | A | upstream_gene_variant | MODIFIER | c.-238G>A| |
S289 |
4 | BAA10g01970 | A10 | 943803 | C | T | missense_variant | MODERATE | c.206C>T|p.Ala69Val |
S294 |
5 | BAA10g01970 | A10 | 944495 | G | A | missense_variant | MODERATE | c.604G>A|p.Val202Met |
S112 |
6 | BAA10g01970 | A10 | 944998 | C | T | synonymous_variant | LOW | c.765C>T|p.Asp255Asp |
S165 |
7 | BAA10g01970 | A10 | 945318 | G | A | synonymous_variant | LOW | c.906G>A|p.Glu302Glu |
S208 S219 |
8 | BAA10g01970 | A10 | 945692 | C | T | synonymous_variant | LOW | c.1153C>T|p.Leu385Leu |
S123 |
9 | BAA10g01970 | A10 | 945854 | G | A | missense_variant | MODERATE | c.1315G>A|p.Ala439Thr |
S80 |
10 | BAA10g01970 | A10 | 948736 | C | T | downstream_gene_variant | MODIFIER | c.*2675C>T| |
S247 |
11 | BAA10g01970 | A10 | 949543 | G | A | downstream_gene_variant | MODIFIER | c.*3482G>A| |
S32 |
12 | BAA10g01970 | A10 | 949555 | G | A | downstream_gene_variant | MODIFIER | c.*3494G>A| |
S167 |
13 | BAA10g01970 | A10 | 950831 | G | T | downstream_gene_variant | MODIFIER | c.*4770G>T| |
S107 S142 S166 S168 |