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
98201 BAA10g05870 A10 3001505 G A downstream_gene_variant MODIFIER c.*2727C>T| S151
S263
98202 BAA10g05870 A10 3001637 G A downstream_gene_variant MODIFIER c.*2595C>T| S18
98203 BAA10g05870 A10 3003185 G A downstream_gene_variant MODIFIER c.*1047C>T| S62
98204 BAA10g05870 A10 3003217 C T downstream_gene_variant MODIFIER c.*1015G>A| S157
S163
98205 BAA10g05870 A10 3003525 C T downstream_gene_variant MODIFIER c.*707G>A| S232
98206 BAA10g05870 A10 3003696 G A downstream_gene_variant MODIFIER c.*536C>T| S290
98207 BAA10g05870 A10 3004156 C T downstream_gene_variant MODIFIER c.*76G>A| S119
98208 BAA10g05870 A10 3004503 G A intron_variant MODIFIER c.2083-9C>T| S264
98209 BAA10g05870 A10 3004506 C T intron_variant MODIFIER c.2083-12G>A| S104
S52
98210 BAA10g05870 A10 3005119 C T intron_variant MODIFIER c.1949+76G>A| S169
98211 BAA10g05880 A10 3006076 C T upstream_gene_variant MODIFIER c.-4184C>T| S246
98212 BAA10g05870 A10 3006249 G A missense_variant MODERATE c.1598C>T|p.Pro533Leu S19
98213 BAA10g05870 A10 3007463 G A splice_region_variant&synonymous_variant LOW c.1134C>T|p.Tyr378Tyr S262
98214 BAA10g05870 A10 3008072 G A missense_variant MODERATE c.869C>T|p.Pro290Leu S94
98215 BAA10g05870 A10 3008591 G A missense_variant MODERATE c.512C>T|p.Pro171Leu S65
98216 BAA10g05870 A10 3009346 G A upstream_gene_variant MODIFIER c.-56C>T| S117
98217 BAA10g05870 A10 3009592 G A upstream_gene_variant MODIFIER c.-302C>T| S57
98218 BAA10g05870 A10 3009789 C T upstream_gene_variant MODIFIER c.-499G>A| S244
98219 BAA10g05870 A10 3011115 G A upstream_gene_variant MODIFIER c.-1825C>T| S25
98220 BAA10g05870 A10 3011325 C T upstream_gene_variant MODIFIER c.-2035G>A| S15
S4
S6
98221 BAA10g05870 A10 3012161 G A upstream_gene_variant MODIFIER c.-2871C>T| S82
S92
98222 BAA10g05870 A10 3012878 G A upstream_gene_variant MODIFIER c.-3588C>T| S53
98223 BAA10g05890 A10 3013791 C T missense_variant MODERATE c.583G>A|p.Gly195Ser S152
98224 BAA10g05890 A10 3013833 C T missense_variant MODERATE c.541G>A|p.Gly181Arg S281
98225 BAA10g05890 A10 3014448 G A upstream_gene_variant MODIFIER c.-75C>T| S165