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
135101 BAA10g21100 A10 18687199 C T upstream_gene_variant MODIFIER c.-1179G>A| S216
135102 BAA10g21100 A10 18687612 C T upstream_gene_variant MODIFIER c.-1592G>A| S87
135103 BAA10g21110 A10 18688830 G A synonymous_variant LOW c.510G>A|p.Gln170Gln S69
135104 BAA10g21110 A10 18688953 C T synonymous_variant LOW c.633C>T|p.Phe211Phe S11
135105 BAA10g21110 A10 18689755 G A missense_variant MODERATE c.1102G>A|p.Glu368Lys S273
135106 BAA10g21110 A10 18690261 G A missense_variant MODERATE c.1445G>A|p.Gly482Glu S16
135107 BAA10g21100 A10 18690865 G A upstream_gene_variant MODIFIER c.-4845C>T| S182
135108 BAA10g21120 A10 18691201 G A missense_variant MODERATE c.1124C>T|p.Ser375Phe S17
135109 BAA10g21120 A10 18691458 G A missense_variant MODERATE c.959C>T|p.Ala320Val S149
135110 BAA10g21120 A10 18692380 G A synonymous_variant LOW c.411C>T|p.His137His S134
135111 BAA10g21120 A10 18693539 C T upstream_gene_variant MODIFIER c.-442G>A| S153
S213
135112 BAA10g21120 A10 18694280 C T upstream_gene_variant MODIFIER c.-1183G>A| S83
S88
135113 BAA10g21130 A10 18696573 C T missense_variant MODERATE c.442C>T|p.Arg148Cys S281
135114 BAA10g21130 A10 18696777 G A missense_variant MODERATE c.646G>A|p.Gly216Arg S293
135115 BAA10g21140 A10 18698414 G A upstream_gene_variant MODIFIER c.-2142G>A| S262
135116 BAA10g21140 A10 18700096 G A upstream_gene_variant MODIFIER c.-460G>A| S131
135117 BAA10g21140 A10 18700422 G A upstream_gene_variant MODIFIER c.-134G>A| S122
135118 BAA10g21140 A10 18701035 G A synonymous_variant LOW c.384G>A|p.Glu128Glu S261
135119 BAA10g21140 A10 18701344 G A missense_variant MODERATE c.590G>A|p.Arg197His S57
135120 BAA10g21140 A10 18701939 G A intron_variant MODIFIER c.887+31G>A| S213
135121 BAA10g21140 A10 18701999 C T intron_variant MODIFIER c.888-9C>T| S98
135122 BAA10g21140 A10 18702239 C T intron_variant MODIFIER c.964-28C>T| S11
135123 BAA10g21140 A10 18703642 C T intron_variant MODIFIER c.1594-21C>T| S150
135124 BAA10g21150 A10 18707145 G A upstream_gene_variant MODIFIER c.-1915G>A| S210
135125 BAA10g21150 A10 18707966 C T upstream_gene_variant MODIFIER c.-1094C>T| S224