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
111801 BAA10g08370 A10 10122725 C T upstream_gene_variant MODIFIER c.-4904G>A| S273
111802 BAA10g08380 A10 10123553 C T downstream_gene_variant MODIFIER c.*3547G>A| S183
111803 BAA10g08380 A10 10124912 G A downstream_gene_variant MODIFIER c.*2188C>T| S262
111804 BAA10g08380 A10 10124983 C T downstream_gene_variant MODIFIER c.*2117G>A| S124
111805 BAA10g08380 A10 10125018 C T downstream_gene_variant MODIFIER c.*2082G>A| S193
111806 BAA10g08380 A10 10127918 G A upstream_gene_variant MODIFIER c.-490C>T| S237
111807 BAA10g08380 A10 10128218 G A upstream_gene_variant MODIFIER c.-790C>T| S112
111808 BAA10g08380 A10 10128264 G A upstream_gene_variant MODIFIER c.-836C>T| S45
111809 BAA10g08380 A10 10128386 G A upstream_gene_variant MODIFIER c.-958C>T| S257
111810 BAA10g08380 A10 10128451 G A upstream_gene_variant MODIFIER c.-1023C>T| S289
111811 BAA10g08380 A10 10129240 C T upstream_gene_variant MODIFIER c.-1812G>A| S225
111812 BAA10g08380 A10 10129389 G A upstream_gene_variant MODIFIER c.-1961C>T| S180
111813 BAA10g08380 A10 10129426 C T upstream_gene_variant MODIFIER c.-1998G>A| S174
S27
111814 BAA10g08380 A10 10129792 G A upstream_gene_variant MODIFIER c.-2364C>T| S57
111815 BAA10g08390 A10 10132656 G A downstream_gene_variant MODIFIER c.*775C>T| S226
111816 BAA10g08390 A10 10133459 G A missense_variant MODERATE c.2873C>T|p.Ser958Phe S69
111817 BAA10g08390 A10 10133698 C T stop_gained HIGH c.2634G>A|p.Trp878* S244
111818 BAA10g08390 A10 10134148 C T intron_variant MODIFIER c.2503+54G>A| S193
111819 BAA10g08390 A10 10134542 G A synonymous_variant LOW c.2163C>T|p.Ile721Ile S295
111820 BAA10g08390 A10 10134644 C T stop_gained HIGH c.2061G>A|p.Trp687* S203
111821 BAA10g08390 A10 10134826 C T missense_variant MODERATE c.1879G>A|p.Asp627Asn S206
S26
111822 BAA10g08390 A10 10134932 C T synonymous_variant LOW c.1773G>A|p.Leu591Leu S67
111823 BAA10g08390 A10 10135306 G A missense_variant MODERATE c.1399C>T|p.Leu467Phe S67
111824 BAA10g08390 A10 10135316 C T synonymous_variant LOW c.1389G>A|p.Val463Val S79
S91
111825 BAA10g08390 A10 10135758 C T missense_variant MODERATE c.947G>A|p.Arg316Lys S297