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
159101 BAA02g06580 A02 2802911 C T upstream_gene_variant MODIFIER c.-2589C>T| S46
159102 BAA02g06580 A02 2803054 C T upstream_gene_variant MODIFIER c.-2446C>T| S95
159103 BAA02g06580 A02 2803073 G A upstream_gene_variant MODIFIER c.-2427G>A| S41
159104 BAA02g06580 A02 2803172 C T upstream_gene_variant MODIFIER c.-2328C>T| S216
159105 BAA02g06580 A02 2803459 C T upstream_gene_variant MODIFIER c.-2041C>T| S112
159106 BAA02g06580 A02 2805656 G A missense_variant MODERATE c.157G>A|p.Gly53Arg S12
159107 BAA02g06580 A02 2805667 G A synonymous_variant LOW c.168G>A|p.Thr56Thr S127
159108 BAA02g06580 A02 2806719 C T missense_variant MODERATE c.542C>T|p.Pro181Leu S13
159109 BAA02g06590 A02 2807415 C T upstream_gene_variant MODIFIER c.-731C>T| S267
159110 BAA02g06580 A02 2808765 C T downstream_gene_variant MODIFIER c.*1423C>T| S295
159111 BAA02g06600 A02 2811069 C T missense_variant MODERATE c.5947G>A|p.Gly1983Ser S37
159112 BAA02g06600 A02 2812332 G A missense_variant MODERATE c.4684C>T|p.Leu1562Phe S294
159113 BAA02g06600 A02 2812344 C T missense_variant MODERATE c.4672G>A|p.Ala1558Thr S32
159114 BAA02g06600 A02 2814363 C T missense_variant MODERATE c.2827G>A|p.Ala943Thr S174
159115 BAA02g06600 A02 2815283 G A missense_variant MODERATE c.2404C>T|p.Pro802Ser S269
159116 BAA02g06600 A02 2816923 G A missense_variant MODERATE c.1439C>T|p.Thr480Ile S292
S9
159117 BAA02g06610 A02 2817747 C T downstream_gene_variant MODIFIER c.*2994G>A| S234
159118 BAA02g06600 A02 2817847 C T stop_gained HIGH c.845G>A|p.Trp282* S203
159119 BAA02g06600 A02 2817870 G A synonymous_variant LOW c.822C>T|p.Arg274Arg S59
159120 BAA02g06600 A02 2818400 G A missense_variant MODERATE c.481C>T|p.Arg161Cys S302
159121 BAA02g06610 A02 2818549 G A downstream_gene_variant MODIFIER c.*2192C>T| S271
159122 BAA02g06610 A02 2821162 G A synonymous_variant LOW c.2793C>T|p.Cys931Cys S294
159123 BAA02g06600 A02 2821477 G A upstream_gene_variant MODIFIER c.-2058C>T| S174
159124 BAA02g06610 A02 2821501 G A splice_region_variant&intron_variant LOW c.2655+7C>T| S236
159125 BAA02g06600 A02 2822536 C T upstream_gene_variant MODIFIER c.-3117G>A| S207