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
157301 BAA02g05020 A02 2204689 G A downstream_gene_variant MODIFIER c.*2022G>A| S122
157302 BAA02g05020 A02 2205204 C T downstream_gene_variant MODIFIER c.*2537C>T| S218
157303 BAA02g05020 A02 2205553 G A downstream_gene_variant MODIFIER c.*2886G>A| S169
157304 BAA02g05020 A02 2205782 C T downstream_gene_variant MODIFIER c.*3115C>T| S240
157305 BAA02g05020 A02 2206404 C T downstream_gene_variant MODIFIER c.*3737C>T| S6
157306 BAA02g05030 A02 2208846 G A downstream_gene_variant MODIFIER c.*4078C>T| S136
157307 BAA02g05030 A02 2209545 C T downstream_gene_variant MODIFIER c.*3379G>A| S188
157308 BAA02g05030 A02 2210256 G A downstream_gene_variant MODIFIER c.*2668C>T| S52
157309 BAA02g05030 A02 2210597 G A downstream_gene_variant MODIFIER c.*2327C>T| S84
S93
157310 BAA02g05030 A02 2210918 C T downstream_gene_variant MODIFIER c.*2006G>A| S178
157311 BAA02g05030 A02 2211084 G A downstream_gene_variant MODIFIER c.*1840C>T| S170
157312 BAA02g05030 A02 2211136 G A downstream_gene_variant MODIFIER c.*1788C>T| S170
157313 BAA02g05030 A02 2211982 C T downstream_gene_variant MODIFIER c.*942G>A| S196
157314 BAA02g05030 A02 2212321 C T downstream_gene_variant MODIFIER c.*603G>A| S167
157315 BAA02g05030 A02 2212810 G A downstream_gene_variant MODIFIER c.*114C>T| S288
157316 BAA02g05040 A02 2213310 G A downstream_gene_variant MODIFIER c.*1388C>T| S62
157317 BAA02g05040 A02 2213392 C T downstream_gene_variant MODIFIER c.*1306G>A| S39
157318 BAA02g05040 A02 2214751 C T missense_variant MODERATE c.541G>A|p.Glu181Lys S156
S34
S4
S6
157319 BAA02g05040 A02 2215158 C T missense_variant MODERATE c.134G>A|p.Arg45Lys S167
157320 BAA02g05040 A02 2215289 C T start_lost HIGH c.3G>A|p.Met1? S293
157321 BAA02g05030 A02 2215360 C T upstream_gene_variant MODIFIER c.-1249G>A| S6
157322 BAA02g05030 A02 2217921 C T upstream_gene_variant MODIFIER c.-3810G>A| S284
157323 BAA02g05060 A02 2219988 C T missense_variant MODERATE c.1126G>A|p.Ala376Thr S263
157324 BAA02g05060 A02 2220690 G A missense_variant MODERATE c.424C>T|p.Leu142Phe S263
157325 BAA02g05060 A02 2220712 C A missense_variant MODERATE c.402G>T|p.Leu134Phe S298