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
131101 BAA10g18490 A10 17284384 C T upstream_gene_variant MODIFIER c.-4948G>A| S282
131102 BAA10g18500 A10 17284711 C T upstream_gene_variant MODIFIER c.-910G>A| S117
131103 BAA10g18500 A10 17286477 G A upstream_gene_variant MODIFIER c.-2676C>T| S278
131104 BAA10g18500 A10 17287636 C T upstream_gene_variant MODIFIER c.-3835G>A| S142
131105 BAA10g18510 A10 17288822 C T downstream_gene_variant MODIFIER c.*23C>T| S68
131106 BAA10g18510 A10 17288831 A G downstream_gene_variant MODIFIER c.*32A>G| S272
131107 BAA10g18510-BAA10g18520 A10 17295180 T C intergenic_region MODIFIER n.17295180T>C| S166
S167
S236
S257
S262
131108 BAA10g18510-BAA10g18520 A10 17295215 G C intergenic_region MODIFIER n.17295215G>C| S16
131109 BAA10g18510-BAA10g18520 A10 17297620 G A intergenic_region MODIFIER n.17297620G>A| S160
131110 BAA10g18510-BAA10g18520 A10 17298814 C T intergenic_region MODIFIER n.17298814C>T| S73
S91
131111 BAA10g18510-BAA10g18520 A10 17299033 C T intergenic_region MODIFIER n.17299033C>T| S48
131112 BAA10g18510-BAA10g18520 A10 17299425 C T intergenic_region MODIFIER n.17299425C>T| S174
S216
S241
S265
131113 BAA10g18510-BAA10g18520 A10 17299760 C T intergenic_region MODIFIER n.17299760C>T| S68
131114 BAA10g18510-BAA10g18520 A10 17302234 G A intergenic_region MODIFIER n.17302234G>A| S174
S27
131115 BAA10g18510-BAA10g18520 A10 17302637 G A intergenic_region MODIFIER n.17302637G>A| S182
131116 BAA10g18520 A10 17303202 C T upstream_gene_variant MODIFIER c.-4446C>T| S19
131117 BAA10g18520 A10 17303494 G A upstream_gene_variant MODIFIER c.-4154G>A| S267
131118 BAA10g18520 A10 17305254 C T upstream_gene_variant MODIFIER c.-2394C>T| S20
131119 BAA10g18520 A10 17306076 C T upstream_gene_variant MODIFIER c.-1572C>T| S174
S27
S39
131120 BAA10g18520 A10 17309229 G A missense_variant&splice_region_variant MODERATE c.1012G>A|p.Glu338Lys S286
131121 BAA10g18520 A10 17310814 C T missense_variant MODERATE c.1852C>T|p.Pro618Ser S61
131122 BAA10g18520 A10 17311399 G A missense_variant MODERATE c.2272G>A|p.Glu758Lys S203
131123 BAA10g18520 A10 17311715 C T missense_variant MODERATE c.2518C>T|p.Leu840Phe S247
131124 BAA10g18530 A10 17313277 G A splice_region_variant&intron_variant LOW c.1787-3C>T| S162
131125 BAA10g18530 A10 17314284 G A synonymous_variant LOW c.1110C>T|p.His370His S172
S217