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
134601 BAA10g20760 A10 18527712 C T upstream_gene_variant MODIFIER c.-4659G>A| S282
134602 BAA10g20760 A10 18527921 C T upstream_gene_variant MODIFIER c.-4868G>A| S20
134603 BAA10g20770 A10 18528008 G A missense_variant MODERATE c.832G>A|p.Gly278Arg S278
134604 BAA10g20770 A10 18528588 G A downstream_gene_variant MODIFIER c.*68G>A| S293
134605 BAA10g20770 A10 18528898 T C downstream_gene_variant MODIFIER c.*378T>C| S119
134606 BAA10g20780 A10 18532229 C T missense_variant MODERATE c.1475G>A|p.Gly492Asp S173
134607 BAA10g20780 A10 18532361 G T missense_variant MODERATE c.1343C>A|p.Ala448Glu S61
134608 BAA10g20780 A10 18532892 C T missense_variant MODERATE c.812G>A|p.Gly271Glu S133
134609 BAA10g20780 A10 18533801 C T upstream_gene_variant MODIFIER c.-98G>A| S125
134610 BAA10g20780 A10 18533852 G A upstream_gene_variant MODIFIER c.-149C>T| S118
134611 BAA10g20780 A10 18533948 G A upstream_gene_variant MODIFIER c.-245C>T| S128
134612 BAA10g20780 A10 18535425 C T upstream_gene_variant MODIFIER c.-1722G>A| S199
134613 BAA10g20780 A10 18536724 C T upstream_gene_variant MODIFIER c.-3021G>A| S183
134614 BAA10g20790 A10 18539034 C T missense_variant MODERATE c.1994G>A|p.Gly665Glu S155
134615 BAA10g20790 A10 18539344 C T missense_variant MODERATE c.1765G>A|p.Asp589Asn S286
134616 BAA10g20790 A10 18539363 C T splice_region_variant&intron_variant LOW c.1750-4G>A| S113
134617 BAA10g20790 A10 18539473 C T missense_variant MODERATE c.1741G>A|p.Asp581Asn S95
134618 BAA10g20790 A10 18540726 C T splice_region_variant&intron_variant LOW c.1034+8G>A| S266
134619 BAA10g20800 A10 18541592 G A downstream_gene_variant MODIFIER c.*3217C>T| S64
134620 BAA10g20800 A10 18542531 C T downstream_gene_variant MODIFIER c.*2278G>A| S297
134621 BAA10g20790 A10 18543244 G A synonymous_variant LOW c.216C>T|p.Tyr72Tyr S174
S241
134622 BAA10g20790 A10 18543792 G A synonymous_variant LOW c.123C>T|p.Leu41Leu S233
134623 BAA10g20790 A10 18544239 G A upstream_gene_variant MODIFIER c.-325C>T| S159
S243
134624 BAA10g20800 A10 18544888 G A missense_variant&splice_region_variant MODERATE c.908C>T|p.Ala303Val S32
134625 BAA10g20790 A10 18544975 C T upstream_gene_variant MODIFIER c.-1061G>A| S183