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
159601 BAA02g06950 A02 2975542 G A upstream_gene_variant MODIFIER c.-2608C>T| S136
159602 BAA02g06970 A02 2976920 G A missense_variant MODERATE c.82G>A|p.Asp28Asn S122
159603 BAA02g06950 A02 2977230 G A upstream_gene_variant MODIFIER c.-4296C>T| S231
159604 BAA02g06980 A02 2978261 C T missense_variant MODERATE c.203C>T|p.Pro68Leu S243
159605 BAA02g06980 A02 2978592 G A splice_acceptor_variant&intron_variant HIGH c.370-1G>A| S246
159606 BAA02g06980 A02 2978683 C T missense_variant MODERATE c.460C>T|p.Leu154Phe S78
159607 BAA02g06970 A02 2980293 C T downstream_gene_variant MODIFIER c.*3134C>T| S301
S304
159608 BAA02g06990 A02 2980569 G A synonymous_variant LOW c.984C>T|p.Asn328Asn S140
159609 BAA02g06990 A02 2980636 C T missense_variant MODERATE c.917G>A|p.Arg306Lys S249
159610 BAA02g06980 A02 2982935 C T downstream_gene_variant MODIFIER c.*3894C>T| S44
159611 BAA02g06980 A02 2983358 G A downstream_gene_variant MODIFIER c.*4317G>A| S297
159612 BAA02g06990 A02 2984892 C T missense_variant MODERATE c.512G>A|p.Gly171Asp S293
159613 BAA02g06990 A02 2985054 C T missense_variant MODERATE c.350G>A|p.Arg117Lys S19
159614 BAA02g06990 A02 2986039 C T upstream_gene_variant MODIFIER c.-636G>A| S226
159615 BAA02g06990 A02 2987578 G A upstream_gene_variant MODIFIER c.-2175C>T| S266
159616 BAA02g06990 A02 2988280 G A upstream_gene_variant MODIFIER c.-2877C>T| S126
159617 BAA02g06990 A02 2989110 C T upstream_gene_variant MODIFIER c.-3707G>A| S299
159618 BAA02g06990 A02 2989441 G T upstream_gene_variant MODIFIER c.-4038C>A| S8
159619 BAA02g07000 A02 2992706 G A downstream_gene_variant MODIFIER c.*1508C>T| S237
159620 BAA02g07000 A02 2993352 C T downstream_gene_variant MODIFIER c.*862G>A| S257
159621 BAA02g07000 A02 2993886 C T downstream_gene_variant MODIFIER c.*328G>A| S19
159622 BAA02g07000 A02 2994294 C T missense_variant MODERATE c.991G>A|p.Asp331Asn S104
159623 BAA02g07000 A02 2995025 C T splice_region_variant&intron_variant LOW c.592-8G>A| S8
159624 BAA02g07000 A02 2995147 G A missense_variant MODERATE c.538C>T|p.Leu180Phe S171
159625 BAA02g07000 A02 2997536 G A upstream_gene_variant MODIFIER c.-976C>T| S266