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
193951 BAA02g27660-BAA02g27670 A02 15577504 G A intergenic_region MODIFIER n.15577504G>A| S13
193952 BAA02g27670 A02 15578712 G A downstream_gene_variant MODIFIER c.*3819C>T| S275
193953 BAA02g27670 A02 15580582 C T downstream_gene_variant MODIFIER c.*1949G>A| S75
S81
193954 BAA02g27670 A02 15581961 G A downstream_gene_variant MODIFIER c.*570C>T| S257
193955 BAA02g27670 A02 15582640 G A missense_variant MODERATE c.2864C>T|p.Thr955Ile S35
193956 BAA02g27670 A02 15583521 G A synonymous_variant LOW c.2589C>T|p.Asp863Asp S228
193957 BAA02g27680 A02 15583606 G A upstream_gene_variant MODIFIER c.-3480G>A| S279
193958 BAA02g27680 A02 15583698 G A upstream_gene_variant MODIFIER c.-3388G>A| S127
193959 BAA02g27670 A02 15584116 C T missense_variant MODERATE c.2209G>A|p.Gly737Ser S157
S163
193960 BAA02g27670 A02 15585550 C T missense_variant MODERATE c.775G>A|p.Glu259Lys S226
193961 BAA02g27670 A02 15585855 C T missense_variant MODERATE c.541G>A|p.Glu181Lys S40
S49
193962 BAA02g27670 A02 15586239 G A missense_variant MODERATE c.157C>T|p.Pro53Ser S155
S211
193963 BAA02g27670 A02 15586511 C T upstream_gene_variant MODIFIER c.-116G>A| S135
193964 BAA02g27670 A02 15586601 G A upstream_gene_variant MODIFIER c.-206C>T| S249
193965 BAA02g27680 A02 15588134 G A synonymous_variant LOW c.519G>A|p.Arg173Arg S166
193966 BAA02g27680 A02 15588777 C T synonymous_variant LOW c.699C>T|p.Phe233Phe S240
193967 BAA02g27680 A02 15588848 C T splice_region_variant&intron_variant LOW c.762+8C>T| S15
193968 BAA02g27690 A02 15590802 G A stop_gained HIGH c.360G>A|p.Trp120* S89
193969 BAA02g27670 A02 15591198 C T upstream_gene_variant MODIFIER c.-4803G>A| S66
193970 BAA02g27680 A02 15591475 C T downstream_gene_variant MODIFIER c.*1920C>T| S305
193971 BAA02g27700 A02 15592386 C T synonymous_variant LOW c.162G>A|p.Glu54Glu S108
193972 BAA02g27710 A02 15594053 C T missense_variant MODERATE c.695G>A|p.Gly232Glu S170
193973 BAA02g27710 A02 15594473 G A missense_variant MODERATE c.362C>T|p.Ser121Phe S67
193974 BAA02g27710 A02 15594661 G A missense_variant MODERATE c.271C>T|p.Leu91Phe S17
193975 BAA02g27710 A02 15594772 G A splice_region_variant&intron_variant LOW c.167-7C>T| S111