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
164351 BAA02g10880 A02 4870617 G A upstream_gene_variant MODIFIER c.-3058C>T| S146
164352 BAA02g10880 A02 4870701 C T upstream_gene_variant MODIFIER c.-3142G>A| S172
S217
164353 BAA02g10880 A02 4871089 G A upstream_gene_variant MODIFIER c.-3530C>T| S9
164354 BAA02g10880 A02 4871197 C T upstream_gene_variant MODIFIER c.-3638G>A| S289
S290
164355 BAA02g10880 A02 4871834 G A upstream_gene_variant MODIFIER c.-4275C>T| S192
164356 BAA02g10890 A02 4872508 C T synonymous_variant LOW c.831G>A|p.Pro277Pro S100
164357 BAA02g10890 A02 4872630 G A missense_variant MODERATE c.709C>T|p.Leu237Phe S162
164358 BAA02g10900 A02 4873206 C T downstream_gene_variant MODIFIER c.*1723G>A| S179
164359 BAA02g10890 A02 4873833 C T synonymous_variant LOW c.189G>A|p.Glu63Glu S182
164360 BAA02g10890 A02 4874162 G A upstream_gene_variant MODIFIER c.-14C>T| S286
164361 BAA02g10890 A02 4874266 G A upstream_gene_variant MODIFIER c.-118C>T| S265
164362 BAA02g10900 A02 4874991 G A synonymous_variant LOW c.1114C>T|p.Leu372Leu S287
164363 BAA02g10890 A02 4876307 C T upstream_gene_variant MODIFIER c.-2159G>A| S75
S81
164364 BAA02g10900 A02 4876545 G A missense_variant MODERATE c.289C>T|p.Pro97Ser S245
164365 BAA02g10890 A02 4877178 G A upstream_gene_variant MODIFIER c.-3030C>T| S166
164366 BAA02g10890 A02 4877549 G A upstream_gene_variant MODIFIER c.-3401C>T| S271
164367 BAA02g10890 A02 4877694 G A upstream_gene_variant MODIFIER c.-3546C>T| S209
164368 BAA02g10890 A02 4878538 C T upstream_gene_variant MODIFIER c.-4390G>A| S115
164369 BAA02g10900 A02 4881374 C T upstream_gene_variant MODIFIER c.-4204G>A| S15
S3
164370 BAA02g10900 A02 4882071 G A upstream_gene_variant MODIFIER c.-4901C>T| S79
S91
164371 BAA02g10910 A02 4882241 G A upstream_gene_variant MODIFIER c.-2733G>A| S282
164372 BAA02g10910 A02 4884886 G A upstream_gene_variant MODIFIER c.-88G>A| S163
164373 BAA02g10910 A02 4885086 C T missense_variant MODERATE c.113C>T|p.Ser38Phe S99
164374 BAA02g10910 A02 4885214 T C intron_variant MODIFIER c.201+40T>C| S289
S290
164375 BAA02g10910 A02 4886086 C T intron_variant MODIFIER c.202-686C>T| S117