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
69101 BAA01g36130 A01 24234478 C T upstream_gene_variant MODIFIER c.-722G>A| S184
69102 BAA01g36130 A01 24235709 C T upstream_gene_variant MODIFIER c.-1953G>A| S293
69103 BAA01g36140 A01 24236280 C T synonymous_variant LOW c.555C>T|p.Ser185Ser S166
69104 BAA01g36140 A01 24236457 C T synonymous_variant LOW c.732C>T|p.His244His S98
69105 BAA01g36140 A01 24236625 G A synonymous_variant LOW c.900G>A|p.Pro300Pro S34
69106 BAA01g36130 A01 24238189 G A upstream_gene_variant MODIFIER c.-4433C>T| S86
69107 BAA01g36130 A01 24238301 G A upstream_gene_variant MODIFIER c.-4545C>T| S109
69108 BAA01g36150 A01 24239333 G A upstream_gene_variant MODIFIER c.-112G>A| S217
69109 BAA01g36150 A01 24240257 G A missense_variant MODERATE c.523G>A|p.Asp175Asn S259
69110 BAA01g36150 A01 24240796 C T synonymous_variant LOW c.886C>T|p.Leu296Leu S215
69111 BAA01g36150 A01 24241513 C T synonymous_variant LOW c.1530C>T|p.Asn510Asn S195
69112 BAA01g36150 A01 24241593 C T missense_variant MODERATE c.1610C>T|p.Ala537Val S301
S304
69113 BAA01g36140 A01 24241803 G A downstream_gene_variant MODIFIER c.*4148G>A| S173
69114 BAA01g36140 A01 24242060 C T downstream_gene_variant MODIFIER c.*4405C>T| S162
69115 BAA01g36160 A01 24243022 G A upstream_gene_variant MODIFIER c.-424C>T| S252
69116 BAA01g36160 A01 24246176 C T upstream_gene_variant MODIFIER c.-3578G>A| S164
69117 BAA01g36170 A01 24246589 G A synonymous_variant LOW c.141C>T|p.Ser47Ser S226
69118 BAA01g36160 A01 24246776 T G upstream_gene_variant MODIFIER c.-4178A>C| S156
S204
S208
S269
S292
S45
S49
S63
69119 BAA01g36180 A01 24247605 C T missense_variant MODERATE c.550G>A|p.Glu184Lys S145
S213
69120 BAA01g36180 A01 24247793 C T stop_gained HIGH c.362G>A|p.Trp121* S233
69121 BAA01g36180 A01 24247957 C T stop_gained HIGH c.198G>A|p.Trp66* S69
69122 BAA01g36170 A01 24250222 C T upstream_gene_variant MODIFIER c.-3493G>A| S39
69123 BAA01g36170 A01 24250365 C T upstream_gene_variant MODIFIER c.-3636G>A| S136
69124 BAA01g36170 A01 24250547 C T upstream_gene_variant MODIFIER c.-3818G>A| S12
69125 BAA01g36170 A01 24251138 C T upstream_gene_variant MODIFIER c.-4409G>A| S23