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
104101 BAA10g07880-BAA10g07890 A10 4980100 G A intergenic_region MODIFIER n.4980100G>A| S268
104102 BAA10g07880-BAA10g07890 A10 4980448 G A intergenic_region MODIFIER n.4980448G>A| S67
104103 BAA10g07880-BAA10g07890 A10 4980964 G A intergenic_region MODIFIER n.4980964G>A| S293
104104 BAA10g07880-BAA10g07890 A10 4981219 A T intergenic_region MODIFIER n.4981219A>T| S104
S52
104105 BAA10g07890 A10 4981545 G A upstream_gene_variant MODIFIER c.-4711G>A| S148
S210
S30
S31
104106 BAA10g07890 A10 4982444 C T upstream_gene_variant MODIFIER c.-3812C>T| S114
104107 BAA10g07890 A10 4983410 G A upstream_gene_variant MODIFIER c.-2846G>A| S75
S81
104108 BAA10g07890 A10 4985506 C T upstream_gene_variant MODIFIER c.-750C>T| S294
104109 BAA10g07890 A10 4986079 C T upstream_gene_variant MODIFIER c.-177C>T| S242
104110 BAA10g07890 A10 4986743 G A intron_variant MODIFIER c.92-10G>A| S36
104111 BAA10g07890 A10 4986982 C T synonymous_variant LOW c.321C>T|p.Asn107Asn S238
104112 BAA10g07890 A10 4987058 C T intron_variant MODIFIER c.325+72C>T| S259
104113 BAA10g07890 A10 4987529 C T intron_variant MODIFIER c.419+279C>T| S136
S186
104114 BAA10g07890 A10 4988025 C T missense_variant MODERATE c.437C>T|p.Thr146Ile S8
104115 BAA10g07890 A10 4988061 C T missense_variant MODERATE c.473C>T|p.Pro158Leu S247
104116 BAA10g07890 A10 4989179 G A downstream_gene_variant MODIFIER c.*83G>A| S130
S160
104117 BAA10g07890 A10 4989918 G A downstream_gene_variant MODIFIER c.*822G>A| S202
104118 BAA10g07890 A10 4990015 G A downstream_gene_variant MODIFIER c.*919G>A| S202
104119 BAA10g07890 A10 4990721 G A downstream_gene_variant MODIFIER c.*1625G>A| S184
104120 BAA10g07890 A10 4991259 C T downstream_gene_variant MODIFIER c.*2163C>T| S10
104121 BAA10g07890 A10 4991724 C T downstream_gene_variant MODIFIER c.*2628C>T| S95
104122 BAA10g07900 A10 4992510 C T upstream_gene_variant MODIFIER c.-4757C>T| S42
104123 BAA10g07900 A10 4995515 G A upstream_gene_variant MODIFIER c.-1752G>A| S125
104124 BAA10g07900 A10 4996860 C T upstream_gene_variant MODIFIER c.-407C>T| S193
104125 BAA10g07900 A10 4996945 G A upstream_gene_variant MODIFIER c.-322G>A| S237