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
101351 BAA10g07210-BAA10g07220 A10 4022136 C T intergenic_region MODIFIER n.4022136C>T| S54
101352 BAA10g07210-BAA10g07220 A10 4022791 G A intergenic_region MODIFIER n.4022791G>A| S283
101353 BAA10g07210-BAA10g07220 A10 4031808 C T intergenic_region MODIFIER n.4031808C>T| S51
101354 BAA10g07210-BAA10g07220 A10 4032021 G A intergenic_region MODIFIER n.4032021G>A| S178
101355 BAA10g07210-BAA10g07220 A10 4032222 G A intergenic_region MODIFIER n.4032222G>A| S262
101356 BAA10g07210-BAA10g07220 A10 4032255 G A intergenic_region MODIFIER n.4032255G>A| S138
101357 BAA10g07210-BAA10g07220 A10 4032648 G A intergenic_region MODIFIER n.4032648G>A| S103
101358 BAA10g07220 A10 4033291 G A upstream_gene_variant MODIFIER c.-4727G>A| S103
101359 BAA10g07220 A10 4034298 G A upstream_gene_variant MODIFIER c.-3720G>A| S219
S72
101360 BAA10g07220 A10 4034343 G A upstream_gene_variant MODIFIER c.-3675G>A| S219
S72
101361 BAA10g07220 A10 4034653 C T upstream_gene_variant MODIFIER c.-3365C>T| S152
101362 BAA10g07220 A10 4035565 T C upstream_gene_variant MODIFIER c.-2453T>C| S140
101363 BAA10g07220 A10 4035887 C T upstream_gene_variant MODIFIER c.-2131C>T| S139
101364 BAA10g07220 A10 4036470 C T upstream_gene_variant MODIFIER c.-1548C>T| S15
S4
S6
101365 BAA10g07220 A10 4036607 C T upstream_gene_variant MODIFIER c.-1411C>T| S113
101366 BAA10g07220 A10 4037763 G A upstream_gene_variant MODIFIER c.-255G>A| S62
101367 BAA10g07220 A10 4038504 G A missense_variant MODERATE c.233G>A|p.Arg78Lys S255
101368 BAA10g07230 A10 4039185 G A upstream_gene_variant MODIFIER c.-1144G>A| S64
101369 BAA10g07230 A10 4039667 G A upstream_gene_variant MODIFIER c.-662G>A| S90
101370 BAA10g07230 A10 4040285 G A upstream_gene_variant MODIFIER c.-44G>A| S59
101371 BAA10g07230 A10 4040412 C T synonymous_variant LOW c.84C>T|p.Ser28Ser S256
101372 BAA10g07230 A10 4040625 C T synonymous_variant LOW c.297C>T|p.Asp99Asp S135
101373 BAA10g07230 A10 4040666 G A missense_variant MODERATE c.338G>A|p.Gly113Glu S16
101374 BAA10g07230 A10 4040776 C T missense_variant MODERATE c.448C>T|p.Pro150Ser S297
101375 BAA10g07230 A10 4041202 G A missense_variant MODERATE c.874G>A|p.Glu292Lys S39