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
163651 BAA02g10310 A02 4578919 C T upstream_gene_variant MODIFIER c.-4673G>A| S121
163652 BAA02g10310 A02 4579184 C T upstream_gene_variant MODIFIER c.-4938G>A| S120
163653 BAA02g10340 A02 4582365 C T missense_variant MODERATE c.571G>A|p.Gly191Ser S289
S290
163654 BAA02g10340 A02 4582713 G A missense_variant MODERATE c.347C>T|p.Ser116Phe S232
163655 BAA02g10340 A02 4583050 C T splice_region_variant&intron_variant LOW c.202+7G>A| S116
163656 BAA02g10340 A02 4585328 G A upstream_gene_variant MODIFIER c.-2070C>T| S193
163657 BAA02g10340 A02 4585993 C T upstream_gene_variant MODIFIER c.-2735G>A| S270
163658 BAA02g10340 A02 4585999 C T upstream_gene_variant MODIFIER c.-2741G>A| S276
163659 BAA02g10340 A02 4586158 G A upstream_gene_variant MODIFIER c.-2900C>T| S229
163660 BAA02g10360 A02 4587570 G A missense_variant MODERATE c.76G>A|p.Glu26Lys S203
163661 BAA02g10360 A02 4587769 G A missense_variant MODERATE c.187G>A|p.Ala63Thr S2
163662 BAA02g10350 A02 4589467 G A upstream_gene_variant MODIFIER c.-4231C>T| S164
163663 BAA02g10370 A02 4590464 G A synonymous_variant LOW c.1056C>T|p.Val352Val S203
163664 BAA02g10360 A02 4591827 G A downstream_gene_variant MODIFIER c.*2563G>A| S105
S106
163665 BAA02g10370 A02 4593147 C T upstream_gene_variant MODIFIER c.-619G>A| S78
S83
163666 BAA02g10380 A02 4595020 G A missense_variant MODERATE c.535C>T|p.His179Tyr S165
163667 BAA02g10370 A02 4596868 G A upstream_gene_variant MODIFIER c.-4340C>T| S2
163668 BAA02g10390 A02 4597781 C T splice_acceptor_variant&intron_variant HIGH c.221-1G>A| S129
163669 BAA02g10390 A02 4598013 G A missense_variant MODERATE c.188C>T|p.Thr63Ile S280
163670 BAA02g10380 A02 4598787 G A upstream_gene_variant MODIFIER c.-2561C>T| S82
S92
163671 BAA02g10380 A02 4598818 C T upstream_gene_variant MODIFIER c.-2592G>A| S270
163672 BAA02g10380 A02 4598852 C T upstream_gene_variant MODIFIER c.-2626G>A| S135
163673 BAA02g10390 A02 4601361 G A upstream_gene_variant MODIFIER c.-3161C>T| S62
163674 BAA02g10400 A02 4601541 C T missense_variant MODERATE c.593G>A|p.Ser198Asn S185
163675 BAA02g10400 A02 4601545 C T missense_variant MODERATE c.589G>A|p.Gly197Arg S139