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
83201 BAA01g44110 A01 29264987 G A missense_variant MODERATE c.887C>T|p.Thr296Ile S172
S217
83202 BAA01g44130 A01 29265528 C T upstream_gene_variant MODIFIER c.-3162C>T| S47
83203 BAA01g44130 A01 29265633 C T upstream_gene_variant MODIFIER c.-3057C>T| S206
S26
83204 BAA01g44110 A01 29267250 C T upstream_gene_variant MODIFIER c.-433G>A| S183
S198
83205 BAA01g44120 A01 29267819 C T synonymous_variant LOW c.231G>A|p.Arg77Arg S170
83206 BAA01g44120 A01 29267938 C T missense_variant MODERATE c.112G>A|p.Asp38Asn S79
83207 BAA01g44110 A01 29268099 C T upstream_gene_variant MODIFIER c.-1282G>A| S11
83208 BAA01g44110 A01 29268409 G A upstream_gene_variant MODIFIER c.-1592C>T| S179
83209 BAA01g44130 A01 29269395 G A missense_variant MODERATE c.616G>A|p.Gly206Ser S80
83210 BAA01g44110 A01 29269537 G A upstream_gene_variant MODIFIER c.-2720C>T| S117
83211 BAA01g44110 A01 29269553 C T upstream_gene_variant MODIFIER c.-2736G>A| S77
S82
83212 BAA01g44130 A01 29269758 G A missense_variant MODERATE c.712G>A|p.Glu238Lys S194
83213 BAA01g44130 A01 29269850 C T synonymous_variant LOW c.804C>T|p.Leu268Leu S159
83214 BAA01g44130 A01 29269868 G A missense_variant MODERATE c.822G>A|p.Met274Ile S79
S91
83215 BAA01g44130 A01 29269947 C T missense_variant MODERATE c.901C>T|p.Pro301Ser S88
83216 BAA01g44130 A01 29270001 G A missense_variant MODERATE c.955G>A|p.Ala319Thr S104
83217 BAA01g44130 A01 29270154 C T missense_variant MODERATE c.1108C>T|p.Pro370Ser S168
83218 BAA01g44130 A01 29272613 C T missense_variant MODERATE c.2608C>T|p.Pro870Ser S41
83219 BAA01g44130 A01 29272650 G A missense_variant MODERATE c.2645G>A|p.Gly882Asp S293
83220 BAA01g44130 A01 29273101 C T downstream_gene_variant MODIFIER c.*285C>T| S165
83221 BAA01g44150 A01 29273345 G A upstream_gene_variant MODIFIER c.-4769G>A| S6
83222 BAA01g44140 A01 29273818 G A synonymous_variant LOW c.2586C>T|p.Val862Val S274
83223 BAA01g44140 A01 29274129 C T missense_variant MODERATE c.2275G>A|p.Val759Met S259
83224 BAA01g44140 A01 29274199 C T synonymous_variant LOW c.2205G>A|p.Arg735Arg S11
83225 BAA01g44140 A01 29274281 G A missense_variant MODERATE c.2123C>T|p.Ser708Phe S250