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
144351 BAA10g29040 A10 22016592 C T upstream_gene_variant MODIFIER c.-2680G>A| S177
144352 BAA10g29060 A10 22017107 C T synonymous_variant LOW c.1260G>A|p.Gly420Gly S168
144353 BAA10g29060 A10 22017411 C T missense_variant MODERATE c.956G>A|p.Gly319Glu S243
144354 BAA10g29060 A10 22018895 C T missense_variant MODERATE c.4G>A|p.Gly2Ser S286
144355 BAA10g29060 A10 22019682 G A upstream_gene_variant MODIFIER c.-784C>T| S219
S72
144356 BAA10g29060 A10 22020698 C T upstream_gene_variant MODIFIER c.-1800G>A| S47
144357 BAA10g29060 A10 22021054 G A upstream_gene_variant MODIFIER c.-2156C>T| S240
144358 BAA10g29060 A10 22021394 C A upstream_gene_variant MODIFIER c.-2496G>T| S158
144359 BAA10g29060 A10 22021838 C T upstream_gene_variant MODIFIER c.-2940G>A| S204
144360 BAA10g29060 A10 22023298 C T upstream_gene_variant MODIFIER c.-4400G>A| S286
144361 BAA10g29060 A10 22023454 G A upstream_gene_variant MODIFIER c.-4556C>T| S32
144362 BAA10g29060 A10 22023601 G A upstream_gene_variant MODIFIER c.-4703C>T| S79
S84
144363 BAA10g29070 A10 22024013 C T upstream_gene_variant MODIFIER c.-2049C>T| S204
144364 BAA10g29070 A10 22024186 C T upstream_gene_variant MODIFIER c.-1876C>T| S250
144365 BAA10g29070 A10 22024221 G A upstream_gene_variant MODIFIER c.-1841G>A| S289
S290
S80
144366 BAA10g29070 A10 22024479 C T upstream_gene_variant MODIFIER c.-1583C>T| S44
144367 BAA10g29070 A10 22024955 C T upstream_gene_variant MODIFIER c.-1107C>T| S260
144368 BAA10g29070 A10 22025035 G A upstream_gene_variant MODIFIER c.-1027G>A| S88
144369 BAA10g29070 A10 22025042 G A upstream_gene_variant MODIFIER c.-1020G>A| S18
144370 BAA10g29070 A10 22026352 G A synonymous_variant LOW c.216G>A|p.Lys72Lys S197
144371 BAA10g29070 A10 22026411 G A missense_variant MODERATE c.275G>A|p.Gly92Glu S231
144372 BAA10g29070 A10 22027044 G A stop_gained HIGH c.816G>A|p.Trp272* S115
144373 BAA10g29080 A10 22028536 C T missense_variant MODERATE c.220G>A|p.Gly74Ser S142
144374 BAA10g29080 A10 22028661 G A missense_variant MODERATE c.176C>T|p.Ser59Phe S77
S82
144375 BAA10g29080 A10 22029208 G A upstream_gene_variant MODIFIER c.-214C>T| S219
S72