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
135301 BAA10g21260 A10 18757791 C T intron_variant MODIFIER c.203+767G>A| S68
135302 BAA10g21260 A10 18758605 G A synonymous_variant LOW c.156C>T|p.Tyr52Tyr S178
135303 BAA10g21260 A10 18760594 G A upstream_gene_variant MODIFIER c.-1834C>T| S198
135304 BAA10g21260 A10 18760714 G A upstream_gene_variant MODIFIER c.-1954C>T| S283
135305 BAA10g21260 A10 18761701 C T upstream_gene_variant MODIFIER c.-2941G>A| S183
135306 BAA10g21260 A10 18761905 G A upstream_gene_variant MODIFIER c.-3145C>T| S71
135307 BAA10g21260 A10 18762230 C T upstream_gene_variant MODIFIER c.-3470G>A| S226
135308 BAA10g21260 A10 18762658 G A upstream_gene_variant MODIFIER c.-3898C>T| S298
135309 BAA10g21260 A10 18762842 C T upstream_gene_variant MODIFIER c.-4082G>A| S34
135310 BAA10g21270 A10 18763823 G A upstream_gene_variant MODIFIER c.-3084G>A| S295
135311 BAA10g21270 A10 18765893 G A upstream_gene_variant MODIFIER c.-1014G>A| S284
135312 BAA10g21270 A10 18766211 G A upstream_gene_variant MODIFIER c.-696G>A| S174
135313 BAA10g21270 A10 18766623 T G upstream_gene_variant MODIFIER c.-284T>G| S27
135314 BAA10g21270 A10 18767938 G A missense_variant MODERATE c.518G>A|p.Gly173Glu S198
135315 BAA10g21270 A10 18768665 C T synonymous_variant LOW c.1161C>T|p.Phe387Phe S77
S82
135316 BAA10g21280 A10 18770190 C T missense_variant MODERATE c.974G>A|p.Gly325Asp S275
135317 BAA10g21280 A10 18770393 C T synonymous_variant LOW c.771G>A|p.Thr257Thr S177
135318 BAA10g21280 A10 18771166 C T upstream_gene_variant MODIFIER c.-3G>A| S60
135319 BAA10g21280 A10 18772073 G A upstream_gene_variant MODIFIER c.-910C>T| S109
135320 BAA10g21280 A10 18772587 G A upstream_gene_variant MODIFIER c.-1424C>T| S90
135321 BAA10g21280 A10 18773844 C T upstream_gene_variant MODIFIER c.-2681G>A| S259
135322 BAA10g21280 A10 18774526 G A upstream_gene_variant MODIFIER c.-3363C>T| S295
135323 BAA10g21290 A10 18774615 G A missense_variant MODERATE c.38G>A|p.Arg13Lys S162
135324 BAA10g21290 A10 18774972 C T missense_variant MODERATE c.395C>T|p.Pro132Leu S91
135325 BAA10g21290 A10 18774998 C T missense_variant MODERATE c.421C>T|p.Leu141Phe S115