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
114101 BAA10g09140 A10 11197276 C T upstream_gene_variant MODIFIER c.-3241C>T| S238
114102 BAA10g09140 A10 11197319 G A upstream_gene_variant MODIFIER c.-3198G>A| S288
114103 BAA10g09140 A10 11198149 C T upstream_gene_variant MODIFIER c.-2368C>T| S11
114104 BAA10g09140 A10 11198406 C T upstream_gene_variant MODIFIER c.-2111C>T| S9
114105 BAA10g09140 A10 11198897 G A upstream_gene_variant MODIFIER c.-1620G>A| S35
114106 BAA10g09140 A10 11199153 C T upstream_gene_variant MODIFIER c.-1364C>T| S175
114107 BAA10g09140 A10 11199294 C T upstream_gene_variant MODIFIER c.-1223C>T| S104
S52
114108 BAA10g09140 A10 11199943 T G upstream_gene_variant MODIFIER c.-574T>G| S249
114109 BAA10g09140 A10 11200390 G A upstream_gene_variant MODIFIER c.-127G>A| S65
114110 BAA10g09150 A10 11201873 C T downstream_gene_variant MODIFIER c.*928G>A| S103
114111 BAA10g09140 A10 11202040 G A synonymous_variant LOW c.1209G>A|p.Glu403Glu S45
114112 BAA10g09140 A10 11202669 G A downstream_gene_variant MODIFIER c.*101G>A| S279
114113 BAA10g09140 A10 11203099 G A downstream_gene_variant MODIFIER c.*531G>A| S271
S48
114114 BAA10g09150 A10 11203333 C T missense_variant MODERATE c.202G>A|p.Ala68Thr S168
114115 BAA10g09150 A10 11205268 G A upstream_gene_variant MODIFIER c.-1646C>T| S216
114116 BAA10g09160 A10 11209587 C T upstream_gene_variant MODIFIER c.-1994C>T| S305
114117 BAA10g09160 A10 11210283 G A upstream_gene_variant MODIFIER c.-1298G>A| S302
114118 BAA10g09160 A10 11211460 C T upstream_gene_variant MODIFIER c.-121C>T| S38
114119 BAA10g09160 A10 11211635 G A missense_variant MODERATE c.55G>A|p.Glu19Lys S179
114120 BAA10g09170 A10 11212437 G A upstream_gene_variant MODIFIER c.-4569G>A| S125
114121 BAA10g09160 A10 11212601 G A synonymous_variant LOW c.417G>A|p.Lys139Lys S262
114122 BAA10g09160 A10 11212679 G A synonymous_variant LOW c.495G>A|p.Glu165Glu S7
114123 BAA10g09160 A10 11212893 C T missense_variant MODERATE c.626C>T|p.Pro209Leu S183
114124 BAA10g09170 A10 11213245 G A upstream_gene_variant MODIFIER c.-3761G>A| S109
114125 BAA10g09170 A10 11213480 C T upstream_gene_variant MODIFIER c.-3526C>T| S113