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
114801 BAA10g09400 A10 11401108 C T upstream_gene_variant MODIFIER c.-774C>T| S287
114802 BAA10g09400 A10 11401490 G A upstream_gene_variant MODIFIER c.-392G>A| S217
114803 BAA10g09400 A10 11401659 G A upstream_gene_variant MODIFIER c.-223G>A| S36
114804 BAA10g09400 A10 11402488 G A missense_variant MODERATE c.607G>A|p.Gly203Ser S237
114805 BAA10g09400 A10 11402533 G A missense_variant MODERATE c.652G>A|p.Glu218Lys S226
114806 BAA10g09400 A10 11404822 C T downstream_gene_variant MODIFIER c.*1090C>T| S193
114807 BAA10g09400 A10 11406035 C T downstream_gene_variant MODIFIER c.*2303C>T| S206
S26
114808 BAA10g09410 A10 11406988 C T synonymous_variant LOW c.159G>A|p.Glu53Glu S183
114809 BAA10g09410 A10 11407326 C T upstream_gene_variant MODIFIER c.-180G>A| S67
114810 BAA10g09410 A10 11407514 G A upstream_gene_variant MODIFIER c.-368C>T| S68
114811 BAA10g09410 A10 11407770 G A upstream_gene_variant MODIFIER c.-624C>T| S66
114812 BAA10g09420 A10 11408056 G A missense_variant MODERATE c.299C>T|p.Ser100Leu S105
S106
114813 BAA10g09420 A10 11408726 C T synonymous_variant LOW c.12G>A|p.Glu4Glu S183
114814 BAA10g09410 A10 11409081 C T upstream_gene_variant MODIFIER c.-1935G>A| S46
114815 BAA10g09410 A10 11409198 G A upstream_gene_variant MODIFIER c.-2052C>T| S36
114816 BAA10g09410 A10 11409713 C T upstream_gene_variant MODIFIER c.-2567G>A| S174
S27
114817 BAA10g09410 A10 11410111 C T upstream_gene_variant MODIFIER c.-2965G>A| S54
114818 BAA10g09410 A10 11410327 G A upstream_gene_variant MODIFIER c.-3181C>T| S148
S30
S31
114819 BAA10g09420 A10 11413022 C T upstream_gene_variant MODIFIER c.-4208G>A| S199
114820 BAA10g09420 A10 11413253 G A upstream_gene_variant MODIFIER c.-4439C>T| S203
114821 BAA10g09420 A10 11413467 G A upstream_gene_variant MODIFIER c.-4653C>T| S59
114822 BAA10g09420 A10 11413504 G A upstream_gene_variant MODIFIER c.-4690C>T| S218
114823 BAA10g09420-BAA10g09430 A10 11414130 C T intergenic_region MODIFIER n.11414130C>T| S269
114824 BAA10g09430 A10 11414573 C T downstream_gene_variant MODIFIER c.*4677G>A| S146
114825 BAA10g09430 A10 11415130 C T downstream_gene_variant MODIFIER c.*4120G>A| S168