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
129801 BAA10g17570 A10 16850632 C T synonymous_variant LOW c.378C>T|p.Gly126Gly S23
129802 BAA10g17570 A10 16850968 G A intron_variant MODIFIER c.460+254G>A| S71
129803 BAA10g17570 A10 16851781 G A intron_variant MODIFIER c.461-286G>A| S79
S84
129804 BAA10g17570 A10 16852765 G A downstream_gene_variant MODIFIER c.*439G>A| S9
129805 BAA10g17570 A10 16852857 G A downstream_gene_variant MODIFIER c.*531G>A| S4
129806 BAA10g17570 A10 16852931 G A downstream_gene_variant MODIFIER c.*605G>A| S178
129807 BAA10g17570 A10 16853684 C T downstream_gene_variant MODIFIER c.*1358C>T| S246
129808 BAA10g17570 A10 16853855 C T downstream_gene_variant MODIFIER c.*1529C>T| S8
129809 BAA10g17570 A10 16854605 G A downstream_gene_variant MODIFIER c.*2279G>A| S66
129810 BAA10g17570 A10 16855775 C T downstream_gene_variant MODIFIER c.*3449C>T| S269
129811 BAA10g17570 A10 16855808 C T downstream_gene_variant MODIFIER c.*3482C>T| S268
129812 BAA10g17570 A10 16856258 G A downstream_gene_variant MODIFIER c.*3932G>A| S75
S81
129813 BAA10g17570 A10 16856494 G A downstream_gene_variant MODIFIER c.*4168G>A| S126
129814 BAA10g17580 A10 16857688 G A upstream_gene_variant MODIFIER c.-4793G>A| S288
129815 BAA10g17580 A10 16862975 C T missense_variant MODERATE c.262C>T|p.Leu88Phe S73
S91
129816 BAA10g17580 A10 16863103 G A splice_region_variant&synonymous_variant LOW c.309G>A|p.Arg103Arg S61
129817 BAA10g17580 A10 16863290 G A missense_variant MODERATE c.496G>A|p.Gly166Ser S74
129818 BAA10g17580 A10 16863617 C T missense_variant MODERATE c.823C>T|p.Arg275Cys S277
S78
S83
129819 BAA10g17590 A10 16864151 G A downstream_gene_variant MODIFIER c.*2409C>T| S134
129820 BAA10g17580 A10 16864566 A G downstream_gene_variant MODIFIER c.*259A>G| S202
129821 BAA10g17590 A10 16866667 G A missense_variant MODERATE c.805C>T|p.Pro269Ser S1
S90
129822 BAA10g17590 A10 16867961 C T missense_variant MODERATE c.125G>A|p.Gly42Glu S275
129823 BAA10g17590 A10 16867992 G A missense_variant MODERATE c.94C>T|p.Pro32Ser S228
129824 BAA10g17590 A10 16868914 C T upstream_gene_variant MODIFIER c.-829G>A| S150
129825 BAA10g17590 A10 16869135 G A upstream_gene_variant MODIFIER c.-1050C>T| S63