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
103551 BAA10g07770-BAA10g07780 A10 4785644 C T intergenic_region MODIFIER n.4785644C>T| S114
103552 BAA10g07770-BAA10g07780 A10 4786104 G A intergenic_region MODIFIER n.4786104G>A| S283
103553 BAA10g07770-BAA10g07780 A10 4786374 G A intergenic_region MODIFIER n.4786374G>A| S181
103554 BAA10g07770-BAA10g07780 A10 4786566 C T intergenic_region MODIFIER n.4786566C>T| S176
103555 BAA10g07770-BAA10g07780 A10 4787300 G A intergenic_region MODIFIER n.4787300G>A| S125
103556 BAA10g07770-BAA10g07780 A10 4787718 C T intergenic_region MODIFIER n.4787718C>T| S263
103557 BAA10g07770-BAA10g07780 A10 4787817 C T intergenic_region MODIFIER n.4787817C>T| S259
103558 BAA10g07770-BAA10g07780 A10 4788780 G A intergenic_region MODIFIER n.4788780G>A| S272
103559 BAA10g07770-BAA10g07780 A10 4789437 G A intergenic_region MODIFIER n.4789437G>A| S293
103560 BAA10g07770-BAA10g07780 A10 4789593 G A intergenic_region MODIFIER n.4789593G>A| S164
103561 BAA10g07780 A10 4793381 T C upstream_gene_variant MODIFIER c.-1723T>C| S5
103562 BAA10g07780 A10 4794030 C T upstream_gene_variant MODIFIER c.-1074C>T| S132
S137
S215
S89
103563 BAA10g07780 A10 4794049 G A upstream_gene_variant MODIFIER c.-1055G>A| S284
103564 BAA10g07780 A10 4794842 G A upstream_gene_variant MODIFIER c.-262G>A| S69
103565 BAA10g07780 A10 4795012 G A upstream_gene_variant MODIFIER c.-92G>A| S293
103566 BAA10g07780 A10 4795139 G A synonymous_variant LOW c.36G>A|p.Lys12Lys S198
103567 BAA10g07780 A10 4795235 C T synonymous_variant LOW c.132C>T|p.Leu44Leu S92
103568 BAA10g07790 A10 4795790 C T downstream_gene_variant MODIFIER c.*4594G>A| S113
103569 BAA10g07780 A10 4798437 C T downstream_gene_variant MODIFIER c.*1963C>T| S244
103570 BAA10g07780 A10 4798597 C T downstream_gene_variant MODIFIER c.*2123C>T| S224
103571 BAA10g07780 A10 4798706 C T downstream_gene_variant MODIFIER c.*2232C>T| S96
103572 BAA10g07780 A10 4798951 C T downstream_gene_variant MODIFIER c.*2477C>T| S9
103573 BAA10g07780 A10 4798959 G A downstream_gene_variant MODIFIER c.*2485G>A| S4
103574 BAA10g07800 A10 4799176 G A upstream_gene_variant MODIFIER c.-4972G>A| S290
103575 BAA10g07800 A10 4799775 C T upstream_gene_variant MODIFIER c.-4373C>T| S169