Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
851 | BAA01g00640 | A01 | 288837 | G | A | upstream_gene_variant | MODIFIER | c.-391G>A| |
S44 |
852 | BAA01g00640 | A01 | 289407 | G | A | synonymous_variant | LOW | c.180G>A|p.Glu60Glu |
S241 |
853 | BAA01g00650 | A01 | 292275 | C | T | upstream_gene_variant | MODIFIER | c.-764C>T| |
S107 |
854 | BAA01g00650 | A01 | 292687 | G | A | upstream_gene_variant | MODIFIER | c.-352G>A| |
S104 S52 |
855 | BAA01g00650 | A01 | 292912 | C | T | upstream_gene_variant | MODIFIER | c.-127C>T| |
S265 |
856 | BAA01g00650 | A01 | 293299 | G | A | synonymous_variant | LOW | c.261G>A|p.Lys87Lys |
S40 |
857 | BAA01g00670 | A01 | 294528 | C | T | upstream_gene_variant | MODIFIER | c.-3165C>T| |
S208 |
858 | BAA01g00650 | A01 | 295098 | C | T | missense_variant | MODERATE | c.1276C>T|p.Pro426Ser |
S166 |
859 | BAA01g00670 | A01 | 295232 | C | T | upstream_gene_variant | MODIFIER | c.-2461C>T| |
S282 |
860 | BAA01g00650 | A01 | 295394 | C | T | synonymous_variant | LOW | c.1479C>T|p.Ile493Ile |
S18 |
861 | BAA01g00650 | A01 | 295539 | G | A | synonymous_variant | LOW | c.1515G>A|p.Glu505Glu |
S217 S248 |
862 | BAA01g00670 | A01 | 295852 | C | T | upstream_gene_variant | MODIFIER | c.-1841C>T| |
S111 |
863 | BAA01g00660 | A01 | 296754 | C | T | missense_variant | MODERATE | c.58G>A|p.Glu20Lys |
S158 |
864 | BAA01g00660 | A01 | 297260 | C | T | upstream_gene_variant | MODIFIER | c.-449G>A| |
S62 |
865 | BAA01g00660 | A01 | 298076 | C | T | upstream_gene_variant | MODIFIER | c.-1265G>A| |
S244 |
866 | BAA01g00670 | A01 | 298443 | C | T | missense_variant | MODERATE | c.302C>T|p.Ser101Phe |
S94 |
867 | BAA01g00660 | A01 | 298842 | G | A | upstream_gene_variant | MODIFIER | c.-2031C>T| |
S230 |
868 | BAA01g00670 | A01 | 298927 | C | T | missense_variant | MODERATE | c.352C>T|p.Pro118Ser |
S132 S137 S215 S89 |
869 | BAA01g00670 | A01 | 298961 | G | A | missense_variant | MODERATE | c.386G>A|p.Gly129Asp |
S9 |
870 | BAA01g00670 | A01 | 299166 | G | A | synonymous_variant | LOW | c.591G>A|p.Lys197Lys |
S108 |
871 | BAA01g00670 | A01 | 299619 | G | A | missense_variant | MODERATE | c.970G>A|p.Asp324Asn |
S73 S91 |
872 | BAA01g00670 | A01 | 299661 | C | T | missense_variant | MODERATE | c.1012C>T|p.Pro338Ser |
S255 |
873 | BAA01g00670 | A01 | 299707 | C | T | missense_variant | MODERATE | c.1058C>T|p.Thr353Ile |
S230 |
874 | BAA01g00660 | A01 | 301469 | G | A | upstream_gene_variant | MODIFIER | c.-4658C>T| |
S116 |
875 | BAA01g00680 | A01 | 302250 | C | T | missense_variant&splice_region_variant | MODERATE | c.233C>T|p.Pro78Leu |
S82 S92 |