Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
7751 | BAA01g06210 | A01 | 2781441 | C | T | upstream_gene_variant | MODIFIER | c.-912G>A| |
S20 |
7752 | BAA01g06220 | A01 | 2782540 | C | T | synonymous_variant | LOW | c.546G>A|p.Glu182Glu |
S132 S137 S215 S89 |
7753 | BAA01g06220 | A01 | 2782760 | G | A | missense_variant | MODERATE | c.401C>T|p.Ser134Phe |
S64 |
7754 | BAA01g06220 | A01 | 2782825 | G | A | synonymous_variant | LOW | c.336C>T|p.Leu112Leu |
S286 |
7755 | BAA01g06220 | A01 | 2783024 | G | A | missense_variant | MODERATE | c.137C>T|p.Ser46Phe |
S28 |
7756 | BAA01g06210 | A01 | 2783573 | G | A | upstream_gene_variant | MODIFIER | c.-3044C>T| |
S15 S3 |
7757 | BAA01g06210 | A01 | 2783778 | C | T | upstream_gene_variant | MODIFIER | c.-3249G>A| |
S225 |
7758 | BAA01g06230 | A01 | 2785985 | C | T | missense_variant | MODERATE | c.2170G>A|p.Glu724Lys |
S48 |
7759 | BAA01g06230 | A01 | 2787263 | C | T | missense_variant | MODERATE | c.892G>A|p.Glu298Lys |
S135 |
7760 | BAA01g06230 | A01 | 2787544 | C | T | missense_variant | MODERATE | c.611G>A|p.Arg204Gln |
S265 S48 |
7761 | BAA01g06230 | A01 | 2788814 | G | A | upstream_gene_variant | MODIFIER | c.-400C>T| |
S306 S308 |
7762 | BAA01g06230 | A01 | 2788883 | G | A | upstream_gene_variant | MODIFIER | c.-469C>T| |
S133 |
7763 | BAA01g06230 | A01 | 2789195 | C | T | upstream_gene_variant | MODIFIER | c.-781G>A| |
S4 |
7764 | BAA01g06230 | A01 | 2789516 | C | T | upstream_gene_variant | MODIFIER | c.-1102G>A| |
S42 |
7765 | BAA01g06240 | A01 | 2789826 | C | T | missense_variant | MODERATE | c.212C>T|p.Pro71Leu |
S166 |
7766 | BAA01g06240 | A01 | 2789873 | C | T | missense_variant | MODERATE | c.259C>T|p.Leu87Phe |
S55 |
7767 | BAA01g06230 | A01 | 2790227 | C | T | upstream_gene_variant | MODIFIER | c.-1813G>A| |
S112 |
7768 | BAA01g06240 | A01 | 2791149 | G | A | stop_gained | HIGH | c.843G>A|p.Trp281* |
S293 |
7769 | BAA01g06230 | A01 | 2791604 | G | A | upstream_gene_variant | MODIFIER | c.-3190C>T| |
S38 |
7770 | BAA01g06240 | A01 | 2792177 | C | T | missense_variant | MODERATE | c.1456C>T|p.Pro486Ser |
S66 |
7771 | BAA01g06230 | A01 | 2792853 | G | A | upstream_gene_variant | MODIFIER | c.-4439C>T| |
S303 |
7772 | BAA01g06240 | A01 | 2792942 | C | T | missense_variant | MODERATE | c.1849C>T|p.Leu617Phe |
S295 |
7773 | BAA01g06230 | A01 | 2793320 | C | T | upstream_gene_variant | MODIFIER | c.-4906G>A| |
S113 |
7774 | BAA01g06240 | A01 | 2793942 | G | A | missense_variant | MODERATE | c.2518G>A|p.Val840Ile |
S178 |
7775 | BAA01g06240 | A01 | 2794255 | G | A | synonymous_variant | LOW | c.2667G>A|p.Lys889Lys |
S197 |