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
100701 BAA10g07000-BAA10g07010 A10 3810086 G A intergenic_region MODIFIER n.3810086G>A| S241
100702 BAA10g07000-BAA10g07010 A10 3810925 C T intergenic_region MODIFIER n.3810925C>T| S200
100703 BAA10g07000-BAA10g07010 A10 3811618 C T intergenic_region MODIFIER n.3811618C>T| S56
100704 BAA10g07000-BAA10g07010 A10 3812462 C A intergenic_region MODIFIER n.3812462C>A| S223
100705 BAA10g07000-BAA10g07010 A10 3813070 C T intergenic_region MODIFIER n.3813070C>T| S56
100706 BAA10g07000-BAA10g07010 A10 3813257 C T intergenic_region MODIFIER n.3813257C>T| S247
100707 BAA10g07000-BAA10g07010 A10 3813261 G A intergenic_region MODIFIER n.3813261G>A| S306
S308
100708 BAA10g07000-BAA10g07010 A10 3814452 C T intergenic_region MODIFIER n.3814452C>T| S143
100709 BAA10g07000-BAA10g07010 A10 3817189 C T intergenic_region MODIFIER n.3817189C>T| S6
100710 BAA10g07000-BAA10g07010 A10 3817979 G A intergenic_region MODIFIER n.3817979G>A| S168
S279
S64
100711 BAA10g07000-BAA10g07010 A10 3818994 C T intergenic_region MODIFIER n.3818994C>T| S247
100712 BAA10g07000-BAA10g07010 A10 3819006 C T intergenic_region MODIFIER n.3819006C>T| S70
100713 BAA10g07010 A10 3819354 G A downstream_gene_variant MODIFIER c.*4939C>T| S209
100714 BAA10g07010 A10 3820695 C T downstream_gene_variant MODIFIER c.*3598G>A| S195
100715 BAA10g07010 A10 3820938 C T downstream_gene_variant MODIFIER c.*3355G>A| S200
100716 BAA10g07010 A10 3821789 G A downstream_gene_variant MODIFIER c.*2504C>T| S55
100717 BAA10g07010 A10 3821822 G A downstream_gene_variant MODIFIER c.*2471C>T| S51
100718 BAA10g07010 A10 3823905 C T downstream_gene_variant MODIFIER c.*388G>A| S297
100719 BAA10g07010 A10 3824161 C T downstream_gene_variant MODIFIER c.*132G>A| S206
S26
100720 BAA10g07010 A10 3824358 C T missense_variant MODERATE c.2935G>A|p.Ala979Thr S193
100721 BAA10g07010 A10 3824489 C T missense_variant MODERATE c.2804G>A|p.Gly935Glu S70
100722 BAA10g07010 A10 3824692 C T synonymous_variant LOW c.2601G>A|p.Gly867Gly S88
100723 BAA10g07010 A10 3825272 C T missense_variant MODERATE c.2509G>A|p.Gly837Arg S166
100724 BAA10g07010 A10 3825304 C T missense_variant MODERATE c.2477G>A|p.Arg826Lys S37
100725 BAA10g07010 A10 3825535 G A intron_variant MODIFIER c.2274-28C>T| S219
S72