Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
4851 | BAA01g03920 | A01 | 1778820 | A | T | upstream_gene_variant | MODIFIER | c.-3572T>A| |
S155 S211 S227 |
4852 | BAA01g03920 | A01 | 1779107 | G | A | upstream_gene_variant | MODIFIER | c.-3859C>T| |
S247 S34 |
4853 | BAA01g03920 | A01 | 1779942 | G | A | upstream_gene_variant | MODIFIER | c.-4694C>T| |
S209 |
4854 | BAA01g03940 | A01 | 1781225 | G | A | upstream_gene_variant | MODIFIER | c.-3589G>A| |
S289 S290 |
4855 | BAA01g03940 | A01 | 1782606 | G | A | upstream_gene_variant | MODIFIER | c.-2208G>A| |
S188 |
4856 | BAA01g03930 | A01 | 1783225 | C | T | missense_variant | MODERATE | c.670G>A|p.Asp224Asn |
S267 |
4857 | BAA01g03930 | A01 | 1784219 | G | A | synonymous_variant | LOW | c.18C>T|p.Asn6Asn |
S240 |
4858 | BAA01g03930 | A01 | 1785692 | C | T | upstream_gene_variant | MODIFIER | c.-1395G>A| |
S166 |
4859 | BAA01g03940 | A01 | 1785785 | G | A | missense_variant | MODERATE | c.317G>A|p.Arg106Lys |
S11 |
4860 | BAA01g03930 | A01 | 1786285 | G | A | upstream_gene_variant | MODIFIER | c.-1988C>T| |
S136 |
4861 | BAA01g03940 | A01 | 1787015 | G | A | missense_variant | MODERATE | c.946G>A|p.Asp316Asn |
S136 |
4862 | BAA01g03950 | A01 | 1788118 | G | A | stop_gained | HIGH | c.1162C>T|p.Gln388* |
S75 S81 |
4863 | BAA01g03950 | A01 | 1788256 | C | T | missense_variant | MODERATE | c.1105G>A|p.Val369Ile |
S166 |
4864 | BAA01g03950 | A01 | 1789896 | C | T | synonymous_variant | LOW | c.285G>A|p.Leu95Leu |
S42 |
4865 | BAA01g03950 | A01 | 1790724 | G | A | upstream_gene_variant | MODIFIER | c.-313C>T| |
S172 S217 |
4866 | BAA01g03950 | A01 | 1790744 | C | T | upstream_gene_variant | MODIFIER | c.-333G>A| |
S71 |
4867 | BAA01g03950 | A01 | 1791640 | G | A | upstream_gene_variant | MODIFIER | c.-1229C>T| |
S202 |
4868 | BAA01g03950 | A01 | 1791680 | C | T | upstream_gene_variant | MODIFIER | c.-1269G>A| |
S255 |
4869 | BAA01g03960 | A01 | 1792453 | C | T | splice_region_variant&intron_variant | LOW | c.876+5G>A| |
S137 |
4870 | BAA01g03950 | A01 | 1794037 | C | T | upstream_gene_variant | MODIFIER | c.-3626G>A| |
S160 |
4871 | BAA01g03950 | A01 | 1794305 | G | A | upstream_gene_variant | MODIFIER | c.-3894C>T| |
S103 |
4872 | BAA01g03960 | A01 | 1797039 | G | A | upstream_gene_variant | MODIFIER | c.-2306C>T| |
S156 S157 S163 |
4873 | BAA01g03990 | A01 | 1800865 | C | T | missense_variant&splice_region_variant | MODERATE | c.121G>A|p.Glu41Lys |
S51 |
4874 | BAA01g03990 | A01 | 1802522 | G | A | upstream_gene_variant | MODIFIER | c.-1374C>T| |
S199 |
4875 | BAA01g04000 | A01 | 1806568 | G | A | missense_variant | MODERATE | c.367C>T|p.Pro123Ser |
S67 |