Users can query the SNP information according to the gene ID.


Gene ID

Results: 1 - 489298 of 489298 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
149201 BAA10g33380 A10 23749882 G A synonymous_variant LOW c.810G>A|p.Lys270Lys S226
149202 BAA10g33390 A10 23752269 C T synonymous_variant LOW c.744C>T|p.Ile248Ile S63
149203 BAA10g33370 A10 23752849 G A upstream_gene_variant MODIFIER c.-4860C>T| S303
149204 BAA10g33400 A10 23753552 G A upstream_gene_variant MODIFIER c.-3781G>A| S183
S198
149205 BAA10g33400 A10 23753754 G A upstream_gene_variant MODIFIER c.-3579G>A| S62
149206 BAA10g33400 A10 23753805 G A upstream_gene_variant MODIFIER c.-3528G>A| S109
149207 BAA10g33400 A10 23753903 C T upstream_gene_variant MODIFIER c.-3430C>T| S292
149208 BAA10g33400 A10 23754059 C T upstream_gene_variant MODIFIER c.-3274C>T| S218
149209 BAA10g33400 A10 23757063 C T upstream_gene_variant MODIFIER c.-270C>T| S13
S219
S279
S72
149210 BAA10g33400 A10 23757133 G A upstream_gene_variant MODIFIER c.-200G>A| S165
149211 BAA10g33400 A10 23757529 G A missense_variant MODERATE c.116G>A|p.Arg39Lys S39
149212 BAA10g33400 A10 23758515 C T missense_variant MODERATE c.859C>T|p.Pro287Ser S123
149213 BAA10g33400 A10 23758854 C T downstream_gene_variant MODIFIER c.*49C>T| S8
149214 BAA10g33400 A10 23758929 G A downstream_gene_variant MODIFIER c.*124G>A| S109
149215 BAA10g33400 A10 23759485 C T downstream_gene_variant MODIFIER c.*680C>T| S306
149216 BAA10g33400 A10 23760202 C T downstream_gene_variant MODIFIER c.*1397C>T| S295
149217 BAA10g33400 A10 23760478 C T downstream_gene_variant MODIFIER c.*1673C>T| S25
149218 BAA10g33400 A10 23760524 G A downstream_gene_variant MODIFIER c.*1719G>A| S105
149219 BAA10g33400 A10 23760624 G A downstream_gene_variant MODIFIER c.*1819G>A| S100
149220 BAA10g33410 A10 23763380 G A upstream_gene_variant MODIFIER c.-1739C>T| S280
149221 BAA10g33410 A10 23765425 C T upstream_gene_variant MODIFIER c.-3784G>A| S105
149222 BAA10g33410 A10 23766410 C T upstream_gene_variant MODIFIER c.-4769G>A| S187
S194
149223 BAA10g33420 A10 23767270 T G upstream_gene_variant MODIFIER c.-4486A>C| S292
149224 BAA10g33430 A10 23770327 G A missense_variant MODERATE c.640G>A|p.Ala214Thr S37
149225 BAA10g33440 A10 23772460 G A upstream_gene_variant MODIFIER c.-288G>A| S293