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
70951 BAA01g37240 A01 24836139 C T missense_variant MODERATE c.364C>T|p.Pro122Ser S161
70952 BAA01g37240 A01 24836160 C T missense_variant MODERATE c.385C>T|p.Pro129Ser S148
S210
70953 BAA01g37240 A01 24836165 C T synonymous_variant LOW c.390C>T|p.Leu130Leu S51
70954 BAA01g37250 A01 24836585 G A downstream_gene_variant MODIFIER c.*2064C>T| S129
70955 BAA01g37250 A01 24836606 C T downstream_gene_variant MODIFIER c.*2043G>A| S28
70956 BAA01g37250 A01 24836641 G A downstream_gene_variant MODIFIER c.*2008C>T| S71
70957 BAA01g37240 A01 24837747 G A stop_gained HIGH c.1119G>A|p.Trp373* S43
70958 BAA01g37240 A01 24838327 T G downstream_gene_variant MODIFIER c.*223T>G| S133
70959 BAA01g37250 A01 24839806 G A upstream_gene_variant MODIFIER c.-441C>T| S35
70960 BAA01g37250 A01 24840184 C T upstream_gene_variant MODIFIER c.-819G>A| S39
70961 BAA01g37250 A01 24840408 G A upstream_gene_variant MODIFIER c.-1043C>T| S187
70962 BAA01g37250 A01 24840675 G A upstream_gene_variant MODIFIER c.-1310C>T| S3
70963 BAA01g37250 A01 24841634 C T upstream_gene_variant MODIFIER c.-2269G>A| S206
S26
70964 BAA01g37250 A01 24842146 C T upstream_gene_variant MODIFIER c.-2781G>A| S123
70965 BAA01g37250 A01 24843114 G A upstream_gene_variant MODIFIER c.-3749C>T| S171
70966 BAA01g37250 A01 24843469 C T upstream_gene_variant MODIFIER c.-4104G>A| S174
S27
70967 BAA01g37250 A01 24843571 C T upstream_gene_variant MODIFIER c.-4206G>A| S89
70968 BAA01g37250 A01 24843602 C T upstream_gene_variant MODIFIER c.-4237G>A| S289
S290
70969 BAA01g37250 A01 24843747 C T upstream_gene_variant MODIFIER c.-4382G>A| S289
S290
70970 BAA01g37250 A01 24844101 C T upstream_gene_variant MODIFIER c.-4736G>A| S293
70971 BAA01g37250-BAA01g37260 A01 24844598 G A intergenic_region MODIFIER n.24844598G>A| S212
70972 BAA01g37250-BAA01g37260 A01 24844744 G A intergenic_region MODIFIER n.24844744G>A| S99
70973 BAA01g37250-BAA01g37260 A01 24844920 C T intergenic_region MODIFIER n.24844920C>T| S302
70974 BAA01g37250-BAA01g37260 A01 24845832 C T intergenic_region MODIFIER n.24845832C>T| S165
70975 BAA01g37250-BAA01g37260 A01 24845952 C T intergenic_region MODIFIER n.24845952C>T| S81
S85