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
51851 BAA01g28680 A01 17984254 G A upstream_gene_variant MODIFIER c.-4938C>T| S63
51852 BAA01g28690 A01 17985082 C T intron_variant MODIFIER c.1167-1880G>A| S272
51853 BAA01g28690 A01 17985726 C T intron_variant MODIFIER c.1166+1845G>A| S282
51854 BAA01g28690 A01 17985999 C T intron_variant MODIFIER c.1166+1572G>A| S28
51855 BAA01g28690 A01 17986180 G A intron_variant MODIFIER c.1166+1391C>T| S85
51856 BAA01g28690 A01 17987006 C T intron_variant MODIFIER c.1166+565G>A| S28
51857 BAA01g28690 A01 17987009 G A intron_variant MODIFIER c.1166+562C>T| S15
S3
51858 BAA01g28690 A01 17987095 A G intron_variant MODIFIER c.1166+476T>C| S299
51859 BAA01g28690 A01 17987739 C T missense_variant MODERATE c.1079G>A|p.Cys360Tyr S200
51860 BAA01g28690 A01 17987750 G A synonymous_variant LOW c.1068C>T|p.Phe356Phe S298
51861 BAA01g28690 A01 17987802 C T missense_variant MODERATE c.1016G>A|p.Arg339Lys S172
S217
51862 BAA01g28690 A01 17988068 C T intron_variant MODIFIER c.884-48G>A| S155
S211
51863 BAA01g28690 A01 17988412 G A intron_variant MODIFIER c.884-392C>T| S217
51864 BAA01g28690 A01 17989155 G A intron_variant MODIFIER c.883+1002C>T| S72
S78
51865 BAA01g28690 A01 17989276 C T intron_variant MODIFIER c.883+881G>A| S48
51866 BAA01g28690 A01 17989419 G A intron_variant MODIFIER c.883+738C>T| S74
51867 BAA01g28690 A01 17989490 C T intron_variant MODIFIER c.883+667G>A| S276
51868 BAA01g28690 A01 17989620 C T intron_variant MODIFIER c.883+537G>A| S18
51869 BAA01g28690 A01 17990110 C T intron_variant MODIFIER c.883+47G>A| S295
51870 BAA01g28690 A01 17990694 G A intron_variant MODIFIER c.685-339C>T| S308
51871 BAA01g28690 A01 17990805 G A intron_variant MODIFIER c.685-450C>T| S265
51872 BAA01g28690 A01 17991066 G A intron_variant MODIFIER c.685-711C>T| S129
51873 BAA01g28690 A01 17991779 A T intron_variant MODIFIER c.684+469T>A| S209
51874 BAA01g28690 A01 17991968 G A intron_variant MODIFIER c.684+280C>T| S236
51875 BAA01g28690 A01 17992276 C T missense_variant MODERATE c.656G>A|p.Gly219Glu S223