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
131801 BAA10g18950 A10 17556836 C T upstream_gene_variant MODIFIER c.-2800G>A| S185
131802 BAA10g18950-BAA10g18960 A10 17559690 G A intergenic_region MODIFIER n.17559690G>A| S288
131803 BAA10g18950-BAA10g18960 A10 17559950 C T intergenic_region MODIFIER n.17559950C>T| S34
131804 BAA10g18950-BAA10g18960 A10 17560400 C T intergenic_region MODIFIER n.17560400C>T| S238
131805 BAA10g18960 A10 17560498 G A downstream_gene_variant MODIFIER c.*4990C>T| S63
131806 BAA10g18960 A10 17560606 C T downstream_gene_variant MODIFIER c.*4882G>A| S70
131807 BAA10g18960 A10 17561708 G A downstream_gene_variant MODIFIER c.*3780C>T| S288
131808 BAA10g18960 A10 17562263 G A downstream_gene_variant MODIFIER c.*3225C>T| S4
131809 BAA10g18960 A10 17565407 G A downstream_gene_variant MODIFIER c.*81C>T| S144
131810 BAA10g18960 A10 17567745 G A upstream_gene_variant MODIFIER c.-1834C>T| S280
131811 BAA10g18960 A10 17568586 G A upstream_gene_variant MODIFIER c.-2675C>T| S9
131812 BAA10g18960 A10 17569299 C T upstream_gene_variant MODIFIER c.-3388G>A| S286
S299
131813 BAA10g18960 A10 17570331 C T upstream_gene_variant MODIFIER c.-4420G>A| S41
131814 BAA10g18960 A10 17570770 C T upstream_gene_variant MODIFIER c.-4859G>A| S173
131815 BAA10g18970 A10 17575300 C T upstream_gene_variant MODIFIER c.-269C>T| S199
131816 BAA10g18970 A10 17575626 G A missense_variant MODERATE c.58G>A|p.Glu20Lys S64
131817 BAA10g18980 A10 17576538 G A upstream_gene_variant MODIFIER c.-3638G>A| S236
131818 BAA10g18970 A10 17576584 C T synonymous_variant LOW c.498C>T|p.Ile166Ile S298
131819 BAA10g18980 A10 17578412 C T upstream_gene_variant MODIFIER c.-1764C>T| S121
131820 BAA10g18980 A10 17579438 G A upstream_gene_variant MODIFIER c.-738G>A| S50
131821 BAA10g18980 A10 17579683 C T upstream_gene_variant MODIFIER c.-493C>T| S259
131822 BAA10g18980 A10 17580408 G A missense_variant MODERATE c.233G>A|p.Arg78Lys S273
131823 BAA10g18980 A10 17580644 G A missense_variant MODERATE c.469G>A|p.Val157Met S223
131824 BAA10g18980 A10 17581214 C T synonymous_variant LOW c.834C>T|p.Thr278Thr S246
131825 BAA10g18980 A10 17583114 C T downstream_gene_variant MODIFIER c.*630C>T| S244