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
95101 BAA10g03890 A10 1905037 G A upstream_gene_variant MODIFIER c.-778C>T| S219
S72
95102 BAA10g03890 A10 1905139 G A upstream_gene_variant MODIFIER c.-880C>T| S156
95103 BAA10g03890 A10 1905534 G A upstream_gene_variant MODIFIER c.-1275C>T| S33
95104 BAA10g03890 A10 1905905 C T upstream_gene_variant MODIFIER c.-1646G>A| S146
95105 BAA10g03890 A10 1906372 C T upstream_gene_variant MODIFIER c.-2113G>A| S276
95106 BAA10g03900 A10 1910004 G A missense_variant MODERATE c.338C>T|p.Pro113Leu S242
95107 BAA10g03910 A10 1910204 C T upstream_gene_variant MODIFIER c.-4800C>T| S84
S93
95108 BAA10g03910 A10 1910226 G A upstream_gene_variant MODIFIER c.-4778G>A| S138
95109 BAA10g03910 A10 1910260 C T upstream_gene_variant MODIFIER c.-4744C>T| S225
95110 BAA10g03910 A10 1911423 C T upstream_gene_variant MODIFIER c.-3581C>T| S23
95111 BAA10g03910 A10 1911523 C T upstream_gene_variant MODIFIER c.-3481C>T| S305
95112 BAA10g03900 A10 1912299 C T upstream_gene_variant MODIFIER c.-372G>A| S42
95113 BAA10g03900 A10 1912616 G A upstream_gene_variant MODIFIER c.-689C>T| S124
95114 BAA10g03900 A10 1913021 C T upstream_gene_variant MODIFIER c.-1094G>A| S162
95115 BAA10g03900 A10 1913169 G A upstream_gene_variant MODIFIER c.-1242C>T| S205
95116 BAA10g03900 A10 1913255 G A upstream_gene_variant MODIFIER c.-1328C>T| S33
95117 BAA10g03910 A10 1915331 C T missense_variant MODERATE c.116C>T|p.Ala39Val S87
95118 BAA10g03910 A10 1915348 C T missense_variant MODERATE c.133C>T|p.Arg45Trp S197
95119 BAA10g03900 A10 1916568 A C upstream_gene_variant MODIFIER c.-4641T>G| S261
95120 BAA10g03910 A10 1917460 G A splice_region_variant&synonymous_variant LOW c.489G>A|p.Gly163Gly S178
95121 BAA10g03910 A10 1919664 C T missense_variant MODERATE c.842C>T|p.Thr281Ile S123
95122 BAA10g03920 A10 1921299 G A missense_variant MODERATE c.758G>A|p.Arg253Lys S46
95123 BAA10g03920 A10 1921655 G A missense_variant MODERATE c.1114G>A|p.Asp372Asn S303
95124 BAA10g03930 A10 1923488 G A missense_variant MODERATE c.1534C>T|p.Pro512Ser S17
95125 BAA10g03930 A10 1924196 C T stop_gained HIGH c.1203G>A|p.Trp401* S166