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
125801 BAA10g14780 A10 15421982 G A upstream_gene_variant MODIFIER c.-3297C>T| S136
125802 BAA10g14780 A10 15423482 C T upstream_gene_variant MODIFIER c.-4797G>A| S8
125803 BAA10g14780 A10 15423501 C T upstream_gene_variant MODIFIER c.-4816G>A| S183
125804 BAA10g14790 A10 15423898 G A upstream_gene_variant MODIFIER c.-3607C>T| S207
125805 BAA10g14800 A10 15424547 G A synonymous_variant LOW c.480C>T|p.Tyr160Tyr S192
125806 BAA10g14800 A10 15424647 G A missense_variant MODERATE c.380C>T|p.Pro127Leu S65
125807 BAA10g14790 A10 15424675 C T upstream_gene_variant MODIFIER c.-4384G>A| S122
125808 BAA10g14800 A10 15425799 C T upstream_gene_variant MODIFIER c.-587G>A| S168
125809 BAA10g14800 A10 15428411 G A upstream_gene_variant MODIFIER c.-3199C>T| S226
125810 BAA10g14800 A10 15428486 C T upstream_gene_variant MODIFIER c.-3274G>A| S8
125811 BAA10g14800 A10 15429002 C T upstream_gene_variant MODIFIER c.-3790G>A| S73
S91
125812 BAA10g14800 A10 15429405 G A upstream_gene_variant MODIFIER c.-4193C>T| S139
125813 BAA10g14800 A10 15429975 G A upstream_gene_variant MODIFIER c.-4763C>T| S292
125814 BAA10g14820 A10 15431746 G A missense_variant MODERATE c.572G>A|p.Ser191Asn S139
125815 BAA10g14820 A10 15432075 C T missense_variant MODERATE c.746C>T|p.Ala249Val S190
125816 BAA10g14830 A10 15432639 A T upstream_gene_variant MODIFIER c.-2460A>T| S107
125817 BAA10g14830 A10 15433955 G A upstream_gene_variant MODIFIER c.-1144G>A| S183
125818 BAA10g14830 A10 15434384 G A upstream_gene_variant MODIFIER c.-715G>A| S295
125819 BAA10g14830 A10 15434928 C T upstream_gene_variant MODIFIER c.-171C>T| S197
125820 BAA10g14830 A10 15435082 G A upstream_gene_variant MODIFIER c.-17G>A| S239
125821 BAA10g14830 A10 15436137 C T synonymous_variant LOW c.1039C>T|p.Leu347Leu S276
125822 BAA10g14840 A10 15436667 G A upstream_gene_variant MODIFIER c.-830G>A| S192
125823 BAA10g14840 A10 15436726 C T upstream_gene_variant MODIFIER c.-771C>T| S233
125824 BAA10g14840 A10 15437665 G A missense_variant MODERATE c.169G>A|p.Val57Met S289
125825 BAA10g14850 A10 15437813 C T upstream_gene_variant MODIFIER c.-3928C>T| S244