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
98101 BAA10g05780 A10 2968015 C T upstream_gene_variant MODIFIER c.-3606G>A| S170
98102 BAA10g05780 A10 2968029 G A upstream_gene_variant MODIFIER c.-3620C>T| S277
98103 BAA10g05790 A10 2971220 C T downstream_gene_variant MODIFIER c.*2096G>A| S87
98104 BAA10g05790 A10 2971438 C T downstream_gene_variant MODIFIER c.*1878G>A| S196
98105 BAA10g05790 A10 2971536 C T downstream_gene_variant MODIFIER c.*1780G>A| S132
S137
S215
S237
S89
98106 BAA10g05790 A10 2972359 C T downstream_gene_variant MODIFIER c.*957G>A| S73
S91
98107 BAA10g05790 A10 2972403 G A downstream_gene_variant MODIFIER c.*913C>T| S198
98108 BAA10g05790 A10 2972688 G A downstream_gene_variant MODIFIER c.*628C>T| S278
98109 BAA10g05790 A10 2972906 G A downstream_gene_variant MODIFIER c.*410C>T| S18
98110 BAA10g05810 A10 2973213 A T upstream_gene_variant MODIFIER c.-4885A>T| S103
98111 BAA10g05790 A10 2973408 G A stop_gained HIGH c.94C>T|p.Arg32* S45
98112 BAA10g05790 A10 2973449 C T missense_variant MODERATE c.53G>A|p.Arg18His S195
98113 BAA10g05790 A10 2974645 G A upstream_gene_variant MODIFIER c.-1144C>T| S280
98114 BAA10g05790 A10 2975213 G A upstream_gene_variant MODIFIER c.-1712C>T| S241
98115 BAA10g05790 A10 2975554 G A upstream_gene_variant MODIFIER c.-2053C>T| S33
98116 BAA10g05790 A10 2975645 G A upstream_gene_variant MODIFIER c.-2144C>T| S218
98117 BAA10g05790 A10 2977941 C T upstream_gene_variant MODIFIER c.-4440G>A| S162
98118 BAA10g05800 A10 2980855 C T upstream_gene_variant MODIFIER c.-3390G>A| S122
98119 BAA10g05820 A10 2982849 G A missense_variant MODERATE c.574C>T|p.Arg192Cys S12
98120 BAA10g05820 A10 2983483 C T synonymous_variant LOW c.33G>A|p.Glu11Glu S149
98121 BAA10g05820 A10 2984367 C T upstream_gene_variant MODIFIER c.-852G>A| S265
98122 BAA10g05820 A10 2984531 G A upstream_gene_variant MODIFIER c.-1016C>T| S242
98123 BAA10g05830 A10 2985167 C T missense_variant MODERATE c.406G>A|p.Ala136Thr S8
98124 BAA10g05830 A10 2985502 C T missense_variant MODERATE c.199G>A|p.Glu67Lys S152
98125 BAA10g05820 A10 2986196 C T upstream_gene_variant MODIFIER c.-2681G>A| S197