Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
2201 | BAA01g01790 | A01 | 817868 | G | A | upstream_gene_variant | MODIFIER | c.-402C>T| |
S234 |
2202 | BAA01g01790 | A01 | 818696 | G | A | upstream_gene_variant | MODIFIER | c.-1230C>T| |
S123 |
2203 | BAA01g01790 | A01 | 818832 | G | A | upstream_gene_variant | MODIFIER | c.-1366C>T| |
S297 |
2204 | BAA01g01790 | A01 | 819451 | G | A | upstream_gene_variant | MODIFIER | c.-1985C>T| |
S104 S52 |
2205 | BAA01g01800 | A01 | 823173 | G | A | missense_variant | MODERATE | c.190C>T|p.Pro64Ser |
S301 S304 |
2206 | BAA01g01800 | A01 | 823347 | G | A | synonymous_variant | LOW | c.16C>T|p.Leu6Leu |
S159 S243 |
2207 | BAA01g01800 | A01 | 823855 | G | A | upstream_gene_variant | MODIFIER | c.-493C>T| |
S279 |
2208 | BAA01g01800 | A01 | 824120 | G | A | upstream_gene_variant | MODIFIER | c.-758C>T| |
S293 S57 |
2209 | BAA01g01800 | A01 | 826042 | G | A | upstream_gene_variant | MODIFIER | c.-2680C>T| |
S1 S161 S228 S244 S90 |
2210 | BAA01g01800 | A01 | 826216 | G | A | upstream_gene_variant | MODIFIER | c.-2854C>T| |
S247 |
2211 | BAA01g01800 | A01 | 827015 | T | C | upstream_gene_variant | MODIFIER | c.-3653A>G| |
S87 |
2212 | BAA01g01800 | A01 | 827495 | C | T | upstream_gene_variant | MODIFIER | c.-4133G>A| |
S269 |
2213 | BAA01g01800 | A01 | 827790 | G | A | upstream_gene_variant | MODIFIER | c.-4428C>T| |
S250 |
2214 | BAA01g01810 | A01 | 828643 | G | A | upstream_gene_variant | MODIFIER | c.-2320G>A| |
S173 |
2215 | BAA01g01810 | A01 | 829297 | G | A | upstream_gene_variant | MODIFIER | c.-1666G>A| |
S134 S193 S274 |
2216 | BAA01g01810 | A01 | 829831 | G | A | upstream_gene_variant | MODIFIER | c.-1132G>A| |
S10 |
2217 | BAA01g01810 | A01 | 830781 | G | A | upstream_gene_variant | MODIFIER | c.-182G>A| |
S162 |
2218 | BAA01g01810 | A01 | 831003 | C | T | missense_variant | MODERATE | c.41C>T|p.Ser14Leu |
S246 |
2219 | BAA01g01810 | A01 | 831146 | G | A | missense_variant | MODERATE | c.184G>A|p.Glu62Lys |
S142 |
2220 | BAA01g01810 | A01 | 831159 | G | A | missense_variant | MODERATE | c.197G>A|p.Arg66Lys |
S199 |
2221 | BAA01g01810 | A01 | 831221 | C | T | missense_variant | MODERATE | c.259C>T|p.Leu87Phe |
S62 |
2222 | BAA01g01810 | A01 | 831530 | G | A | missense_variant | MODERATE | c.568G>A|p.Glu190Lys |
S159 S188 S243 S276 S298 S299 |
2223 | BAA01g01810 | A01 | 831853 | C | T | downstream_gene_variant | MODIFIER | c.*303C>T| |
S41 |
2224 | BAA01g01810 | A01 | 833134 | C | T | downstream_gene_variant | MODIFIER | c.*1584C>T| |
S233 |
2225 | BAA01g01810 | A01 | 833807 | C | T | downstream_gene_variant | MODIFIER | c.*2257C>T| |
S246 |