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
145701 BAA10g30200 A10 22475002 C T splice_region_variant&intron_variant LOW c.1635+8C>T| S103
145702 BAA10g30200 A10 22477631 G A downstream_gene_variant MODIFIER c.*1571G>A| S59
145703 BAA10g30200 A10 22478014 C T downstream_gene_variant MODIFIER c.*1954C>T| S292
145704 BAA10g30200 A10 22478513 C T downstream_gene_variant MODIFIER c.*2453C>T| S232
145705 BAA10g30200 A10 22480344 G A downstream_gene_variant MODIFIER c.*4284G>A| S4
145706 BAA10g30210 A10 22481590 G A downstream_gene_variant MODIFIER c.*4411C>T| S68
145707 BAA10g30210 A10 22482708 C T downstream_gene_variant MODIFIER c.*3293G>A| S142
145708 BAA10g30210 A10 22483139 G A downstream_gene_variant MODIFIER c.*2862C>T| S69
145709 BAA10g30210 A10 22484931 G A downstream_gene_variant MODIFIER c.*1070C>T| S178
145710 BAA10g30210 A10 22485906 G A downstream_gene_variant MODIFIER c.*95C>T| S239
145711 BAA10g30210 A10 22486586 C T synonymous_variant LOW c.444G>A|p.Glu148Glu S11
S133
145712 BAA10g30210 A10 22486668 C T missense_variant MODERATE c.362G>A|p.Ser121Asn S156
145713 BAA10g30210 A10 22486938 G A synonymous_variant LOW c.126C>T|p.Val42Val S294
145714 BAA10g30210 A10 22486978 G A missense_variant MODERATE c.86C>T|p.Ala29Val S80
145715 BAA10g30210 A10 22487156 C T upstream_gene_variant MODIFIER c.-93G>A| S203
145716 BAA10g30210 A10 22487507 C T upstream_gene_variant MODIFIER c.-444G>A| S45
145717 BAA10g30210 A10 22487613 G A upstream_gene_variant MODIFIER c.-550C>T| S38
145718 BAA10g30210 A10 22487660 G A upstream_gene_variant MODIFIER c.-597C>T| S125
145719 BAA10g30210 A10 22488782 G A upstream_gene_variant MODIFIER c.-1719C>T| S132
S137
S215
145720 BAA10g30210 A10 22490057 G A upstream_gene_variant MODIFIER c.-2994C>T| S71
145721 BAA10g30210 A10 22490632 G A upstream_gene_variant MODIFIER c.-3569C>T| S252
145722 BAA10g30210 A10 22491447 C T upstream_gene_variant MODIFIER c.-4384G>A| S246
145723 BAA10g30220 A10 22491616 G A missense_variant MODERATE c.32G>A|p.Gly11Glu S171
145724 BAA10g30220 A10 22491897 C T missense_variant MODERATE c.239C>T|p.Ser80Phe S25
145725 BAA10g30210 A10 22491974 C T upstream_gene_variant MODIFIER c.-4911G>A| S235