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
130501 BAA10g18070 A10 17092686 C T upstream_gene_variant MODIFIER c.-213C>T| S89
130502 BAA10g18060 A10 17094131 G A downstream_gene_variant MODIFIER c.*3379G>A| S166
130503 BAA10g18060 A10 17095359 C T downstream_gene_variant MODIFIER c.*4607C>T| S244
130504 BAA10g18060 A10 17095366 G A downstream_gene_variant MODIFIER c.*4614G>A| S192
130505 BAA10g18060 A10 17095664 G A downstream_gene_variant MODIFIER c.*4912G>A| S295
130506 BAA10g18070 A10 17096032 G A downstream_gene_variant MODIFIER c.*2906G>A| S192
130507 BAA10g18070 A10 17096093 G A downstream_gene_variant MODIFIER c.*2967G>A| S58
130508 BAA10g18070 A10 17096330 G A downstream_gene_variant MODIFIER c.*3204G>A| S174
130509 BAA10g18070 A10 17096592 C T downstream_gene_variant MODIFIER c.*3466C>T| S117
130510 BAA10g18070 A10 17096668 G A downstream_gene_variant MODIFIER c.*3542G>A| S241
130511 BAA10g18070-BAA10g18080 A10 17098292 G A intergenic_region MODIFIER n.17098292G>A| S131
130512 BAA10g18070-BAA10g18080 A10 17098694 G A intergenic_region MODIFIER n.17098694G>A| S161
130513 BAA10g18070-BAA10g18080 A10 17098758 G A intergenic_region MODIFIER n.17098758G>A| S149
130514 BAA10g18080 A10 17099747 G A upstream_gene_variant MODIFIER c.-4911G>A| S262
130515 BAA10g18080 A10 17100158 G A upstream_gene_variant MODIFIER c.-4500G>A| S182
130516 BAA10g18080 A10 17100427 C T upstream_gene_variant MODIFIER c.-4231C>T| S86
130517 BAA10g18080 A10 17101125 C T upstream_gene_variant MODIFIER c.-3533C>T| S162
130518 BAA10g18080 A10 17102566 G A upstream_gene_variant MODIFIER c.-2092G>A| S128
130519 BAA10g18080 A10 17103046 C T upstream_gene_variant MODIFIER c.-1612C>T| S203
130520 BAA10g18080 A10 17103556 G A upstream_gene_variant MODIFIER c.-1102G>A| S295
130521 BAA10g18080 A10 17103799 C T upstream_gene_variant MODIFIER c.-859C>T| S23
130522 BAA10g18080 A10 17105819 C T missense_variant MODERATE c.1162C>T|p.Pro388Ser S174
S27
S39
130523 BAA10g18080 A10 17106812 G A missense_variant MODERATE c.2155G>A|p.Asp719Asn S32
130524 BAA10g18080 A10 17106857 C T synonymous_variant LOW c.2200C>T|p.Leu734Leu S6
130525 BAA10g18090 A10 17107502 G A upstream_gene_variant MODIFIER c.-1465G>A| S111