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
129051 BAA10g17030 A10 16589106 G A upstream_gene_variant MODIFIER c.-4770G>A| S125
129052 BAA10g17030 A10 16590194 C T upstream_gene_variant MODIFIER c.-3682C>T| S143
129053 BAA10g17030 A10 16590458 C T upstream_gene_variant MODIFIER c.-3418C>T| S186
129054 BAA10g17020 A10 16590660 G A synonymous_variant LOW c.462C>T|p.Asn154Asn S139
129055 BAA10g17030 A10 16591097 C T upstream_gene_variant MODIFIER c.-2779C>T| S10
129056 BAA10g17030 A10 16591233 G A upstream_gene_variant MODIFIER c.-2643G>A| S216
129057 BAA10g17030 A10 16591414 G A upstream_gene_variant MODIFIER c.-2462G>A| S283
129058 BAA10g17030 A10 16591505 C T upstream_gene_variant MODIFIER c.-2371C>T| S235
S236
S260
129059 BAA10g17020 A10 16592997 G A synonymous_variant LOW c.105C>T|p.Tyr35Tyr S172
S217
129060 BAA10g17020 A10 16593166 G A upstream_gene_variant MODIFIER c.-65C>T| S9
129061 BAA10g17030 A10 16594048 C T missense_variant MODERATE c.173C>T|p.Ser58Phe S306
S308
129062 BAA10g17030 A10 16594055 G A missense_variant MODERATE c.180G>A|p.Met60Ile S3
129063 BAA10g17030 A10 16594101 G A missense_variant MODERATE c.226G>A|p.Glu76Lys S184
129064 BAA10g17020 A10 16595493 G A upstream_gene_variant MODIFIER c.-2392C>T| S39
129065 BAA10g17020 A10 16595517 G A upstream_gene_variant MODIFIER c.-2416C>T| S16
129066 BAA10g17020 A10 16595775 C T upstream_gene_variant MODIFIER c.-2674G>A| S237
129067 BAA10g17020 A10 16596610 G A upstream_gene_variant MODIFIER c.-3509C>T| S261
129068 BAA10g17050 A10 16598180 G A missense_variant MODERATE c.323G>A|p.Gly108Glu S125
129069 BAA10g17050 A10 16599567 G A missense_variant&splice_region_variant MODERATE c.1480G>A|p.Asp494Asn S291
129070 BAA10g17050 A10 16599695 C T synonymous_variant LOW c.1608C>T|p.Pro536Pro S34
129071 BAA10g17050 A10 16600092 G A missense_variant MODERATE c.1924G>A|p.Val642Met S303
129072 BAA10g17050 A10 16600265 C T synonymous_variant LOW c.2097C>T|p.Tyr699Tyr S142
129073 BAA10g17040 A10 16600782 C T upstream_gene_variant MODIFIER c.-4563G>A| S162
129074 BAA10g17060 A10 16601450 C T synonymous_variant LOW c.729G>A|p.Val243Val S117
129075 BAA10g17060 A10 16601566 C T missense_variant MODERATE c.613G>A|p.Gly205Ser S37