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
29151 BAA01g20560 A01 10146457 G A missense_variant MODERATE c.448C>T|p.Pro150Ser S187
29152 BAA01g20560 A01 10148685 C T upstream_gene_variant MODIFIER c.-1457G>A| S42
29153 BAA01g20570 A01 10150500 G A synonymous_variant LOW c.1209C>T|p.Tyr403Tyr S199
29154 BAA01g20570 A01 10150700 G A missense_variant MODERATE c.1009C>T|p.Pro337Ser S202
29155 BAA01g20570 A01 10150898 G A missense_variant MODERATE c.811C>T|p.Pro271Ser S292
29156 BAA01g20580 A01 10155648 G A missense_variant MODERATE c.307C>T|p.Pro103Ser S59
29157 BAA01g20580 A01 10157057 C T upstream_gene_variant MODIFIER c.-1103G>A| S171
29158 BAA01g20580 A01 10157189 C T upstream_gene_variant MODIFIER c.-1235G>A| S221
29159 BAA01g20580 A01 10157387 C T upstream_gene_variant MODIFIER c.-1433G>A| S136
29160 BAA01g20580 A01 10158319 G A upstream_gene_variant MODIFIER c.-2365C>T| S197
29161 BAA01g20580 A01 10160019 C T upstream_gene_variant MODIFIER c.-4065G>A| S266
29162 BAA01g20580 A01 10160184 G A upstream_gene_variant MODIFIER c.-4230C>T| S59
29163 BAA01g20590 A01 10161256 C T upstream_gene_variant MODIFIER c.-274C>T| S179
29164 BAA01g20590 A01 10161666 G A missense_variant MODERATE c.137G>A|p.Arg46His S108
S79
S91
29165 BAA01g20590 A01 10164198 G A intron_variant MODIFIER c.1171-64G>A| S59
29166 BAA01g20590 A01 10164665 C T downstream_gene_variant MODIFIER c.*146C>T| S38
29167 BAA01g20590 A01 10165517 G A downstream_gene_variant MODIFIER c.*998G>A| S117
29168 BAA01g20590 A01 10167277 C T downstream_gene_variant MODIFIER c.*2758C>T| S135
29169 BAA01g20590 A01 10168750 C T downstream_gene_variant MODIFIER c.*4231C>T| S81
29170 BAA01g20590 A01 10169008 C T downstream_gene_variant MODIFIER c.*4489C>T| S18
29171 BAA01g20590 A01 10169399 G A downstream_gene_variant MODIFIER c.*4880G>A| S6
29172 BAA01g20600 A01 10169713 T G downstream_gene_variant MODIFIER c.*3890A>C| S177
29173 BAA01g20600 A01 10170470 C T downstream_gene_variant MODIFIER c.*3133G>A| S257
29174 BAA01g20600 A01 10170606 C T downstream_gene_variant MODIFIER c.*2997G>A| S11
29175 BAA01g20600 A01 10170696 G A downstream_gene_variant MODIFIER c.*2907C>T| S6