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
140951 BAA10g26070 A10 20790592 C T splice_acceptor_variant&intron_variant HIGH c.1559-1G>A| S123
140952 BAA10g26050 A10 20790884 G A upstream_gene_variant MODIFIER c.-3163C>T| S9
140953 BAA10g26070 A10 20792986 C T splice_region_variant&intron_variant LOW c.651+8G>A| S10
140954 BAA10g26070 A10 20793672 G A synonymous_variant LOW c.291C>T|p.Ser97Ser S287
140955 BAA10g26070 A10 20793762 G A synonymous_variant LOW c.201C>T|p.Val67Val S198
140956 BAA10g26070 A10 20794172 G T upstream_gene_variant MODIFIER c.-210C>A| S171
140957 BAA10g26070 A10 20794899 G A upstream_gene_variant MODIFIER c.-937C>T| S293
140958 BAA10g26070 A10 20795475 C T upstream_gene_variant MODIFIER c.-1513G>A| S113
140959 BAA10g26070 A10 20796799 G A upstream_gene_variant MODIFIER c.-2837C>T| S18
140960 BAA10g26070 A10 20797405 G A upstream_gene_variant MODIFIER c.-3443C>T| S240
140961 BAA10g26070 A10 20797664 C T upstream_gene_variant MODIFIER c.-3702G>A| S177
140962 BAA10g26080 A10 20799495 G A intron_variant MODIFIER c.966+2143C>T| S158
140963 BAA10g26080 A10 20799545 C A intron_variant MODIFIER c.966+2093G>T| S235
S236
S260
140964 BAA10g26080 A10 20801714 C T splice_region_variant&intron_variant LOW c.894-4G>A| S56
140965 BAA10g26080 A10 20804204 C T upstream_gene_variant MODIFIER c.-1374G>A| S37
140966 BAA10g26080 A10 20804888 C T upstream_gene_variant MODIFIER c.-2058G>A| S87
140967 BAA10g26080 A10 20805419 C T upstream_gene_variant MODIFIER c.-2589G>A| S152
140968 BAA10g26080 A10 20806449 C T upstream_gene_variant MODIFIER c.-3619G>A| S121
140969 BAA10g26090 A10 20807972 A T upstream_gene_variant MODIFIER c.-589A>T| S279
140970 BAA10g26090 A10 20808182 C T upstream_gene_variant MODIFIER c.-379C>T| S113
140971 BAA10g26100 A10 20809278 G A downstream_gene_variant MODIFIER c.*1229C>T| S57
140972 BAA10g26090 A10 20809729 G A synonymous_variant LOW c.417G>A|p.Glu139Glu S55
140973 BAA10g26090 A10 20810009 C T synonymous_variant LOW c.531C>T|p.Phe177Phe S44
140974 BAA10g26090 A10 20810161 G A missense_variant MODERATE c.605G>A|p.Ser202Asn S295
140975 BAA10g26100 A10 20810959 C T missense_variant MODERATE c.1945G>A|p.Val649Ile S23