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
112651 BAA10g08600 A10 10427006 C T upstream_gene_variant MODIFIER c.-609G>A| S124
112652 BAA10g08600 A10 10427473 C T upstream_gene_variant MODIFIER c.-1076G>A| S256
112653 BAA10g08600 A10 10427658 G A upstream_gene_variant MODIFIER c.-1261C>T| S125
112654 BAA10g08600 A10 10427717 C T upstream_gene_variant MODIFIER c.-1320G>A| S123
112655 BAA10g08600 A10 10427915 C T upstream_gene_variant MODIFIER c.-1518G>A| S305
112656 BAA10g08600 A10 10428040 C T upstream_gene_variant MODIFIER c.-1643G>A| S25
112657 BAA10g08600 A10 10428053 G A upstream_gene_variant MODIFIER c.-1656C>T| S76
112658 BAA10g08600 A10 10428055 G A upstream_gene_variant MODIFIER c.-1658C>T| S66
112659 BAA10g08600 A10 10428125 C T upstream_gene_variant MODIFIER c.-1728G>A| S155
S211
112660 BAA10g08600 A10 10428729 C T upstream_gene_variant MODIFIER c.-2332G>A| S143
112661 BAA10g08600 A10 10429199 C T upstream_gene_variant MODIFIER c.-2802G>A| S124
112662 BAA10g08600 A10 10430115 G A upstream_gene_variant MODIFIER c.-3718C>T| S159
S243
112663 BAA10g08600-BAA10g08610 A10 10432916 C T intergenic_region MODIFIER n.10432916C>T| S146
112664 BAA10g08600-BAA10g08610 A10 10432961 G A intergenic_region MODIFIER n.10432961G>A| S290
112665 BAA10g08600-BAA10g08610 A10 10433374 C T intergenic_region MODIFIER n.10433374C>T| S133
112666 BAA10g08610 A10 10438033 G A upstream_gene_variant MODIFIER c.-3687G>A| S171
112667 BAA10g08610 A10 10438937 G A upstream_gene_variant MODIFIER c.-2783G>A| S65
112668 BAA10g08610 A10 10439975 G A upstream_gene_variant MODIFIER c.-1745G>A| S15
S3
112669 BAA10g08610 A10 10440196 C T upstream_gene_variant MODIFIER c.-1524C>T| S152
S162
112670 BAA10g08610 A10 10441330 C T upstream_gene_variant MODIFIER c.-390C>T| S155
S211
112671 BAA10g08610 A10 10442000 C T intron_variant MODIFIER c.139+71C>T| S136
S186
112672 BAA10g08610 A10 10442106 G A intron_variant MODIFIER c.139+177G>A| S205
112673 BAA10g08610 A10 10446099 C T downstream_gene_variant MODIFIER c.*3601C>T| S116
112674 BAA10g08610-BAA10g08620 A10 10447765 C T intergenic_region MODIFIER n.10447765C>T| S287
112675 BAA10g08610-BAA10g08620 A10 10447828 C T intergenic_region MODIFIER n.10447828C>T| S37