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
117251 BAA10g10580 A10 12327516 G A synonymous_variant LOW c.1122G>A|p.Thr374Thr S293
117252 BAA10g10590 A10 12330396 C T upstream_gene_variant MODIFIER c.-3719C>T| S166
117253 BAA10g10590 A10 12330554 C T upstream_gene_variant MODIFIER c.-3561C>T| S225
117254 BAA10g10590 A10 12330802 C T upstream_gene_variant MODIFIER c.-3313C>T| S231
117255 BAA10g10590 A10 12330867 C T upstream_gene_variant MODIFIER c.-3248C>T| S287
117256 BAA10g10590 A10 12331193 G A upstream_gene_variant MODIFIER c.-2922G>A| S293
117257 BAA10g10590 A10 12332147 C T upstream_gene_variant MODIFIER c.-1968C>T| S203
117258 BAA10g10590 A10 12333038 G A upstream_gene_variant MODIFIER c.-1077G>A| S160
117259 BAA10g10590 A10 12333426 A T upstream_gene_variant MODIFIER c.-689A>T| S178
117260 BAA10g10590 A10 12333964 G A upstream_gene_variant MODIFIER c.-151G>A| S8
117261 BAA10g10600 A10 12334384 G A upstream_gene_variant MODIFIER c.-4615G>A| S292
117262 BAA10g10600 A10 12334685 C T upstream_gene_variant MODIFIER c.-4314C>T| S199
117263 BAA10g10600 A10 12335080 C T upstream_gene_variant MODIFIER c.-3919C>T| S2
117264 BAA10g10600 A10 12335222 G A upstream_gene_variant MODIFIER c.-3777G>A| S43
117265 BAA10g10600 A10 12335515 G A upstream_gene_variant MODIFIER c.-3484G>A| S279
117266 BAA10g10590 A10 12336794 G A synonymous_variant LOW c.858G>A|p.Glu286Glu S75
S81
117267 BAA10g10600 A10 12337409 G A upstream_gene_variant MODIFIER c.-1590G>A| S67
117268 BAA10g10600 A10 12338186 C T upstream_gene_variant MODIFIER c.-813C>T| S133
117269 BAA10g10600 A10 12339995 G A missense_variant MODERATE c.487G>A|p.Glu163Lys S245
117270 BAA10g10590 A10 12340577 G A downstream_gene_variant MODIFIER c.*3660G>A| S138
117271 BAA10g10600 A10 12340956 G A missense_variant MODERATE c.1145G>A|p.Arg382Lys S172
117272 BAA10g10600 A10 12341056 G A synonymous_variant LOW c.1245G>A|p.Thr415Thr S209
117273 BAA10g10590 A10 12341440 C T downstream_gene_variant MODIFIER c.*4523C>T| S180
117274 BAA10g10590 A10 12341445 G A downstream_gene_variant MODIFIER c.*4528G>A| S136
117275 BAA10g10600 A10 12343151 G A downstream_gene_variant MODIFIER c.*1451G>A| S161