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
113501 BAA10g08900 A10 10907442 G A upstream_gene_variant MODIFIER c.-1446G>A| S192
113502 BAA10g08900 A10 10907766 G A upstream_gene_variant MODIFIER c.-1122G>A| S109
113503 BAA10g08900 A10 10908530 C T upstream_gene_variant MODIFIER c.-358C>T| S8
113504 BAA10g08900 A10 10909102 C T missense_variant MODERATE c.215C>T|p.Thr72Ile S44
113505 BAA10g08900 A10 10909381 C T intron_variant MODIFIER c.284-95C>T| S122
113506 BAA10g08900 A10 10909685 G A missense_variant MODERATE c.397G>A|p.Val133Ile S178
113507 BAA10g08900 A10 10909706 G A missense_variant MODERATE c.418G>A|p.Ala140Thr S45
113508 BAA10g08900 A10 10909743 G A missense_variant MODERATE c.455G>A|p.Gly152Asp S50
113509 BAA10g08910 A10 10910033 C T upstream_gene_variant MODIFIER c.-4768C>T| S166
113510 BAA10g08910 A10 10910071 C T upstream_gene_variant MODIFIER c.-4730C>T| S37
113511 BAA10g08910 A10 10910395 C T upstream_gene_variant MODIFIER c.-4406C>T| S143
113512 BAA10g08910 A10 10910425 C T upstream_gene_variant MODIFIER c.-4376C>T| S298
113513 BAA10g08910 A10 10915038 C T missense_variant MODERATE c.238C>T|p.Pro80Ser S177
113514 BAA10g08920 A10 10918424 C T upstream_gene_variant MODIFIER c.-1036G>A| S168
113515 BAA10g08920 A10 10918541 C T upstream_gene_variant MODIFIER c.-1153G>A| S25
113516 BAA10g08920 A10 10919610 G A upstream_gene_variant MODIFIER c.-2222C>T| S161
113517 BAA10g08920-BAA10g08930 A10 10928681 C T intergenic_region MODIFIER n.10928681C>T| S8
113518 BAA10g08920-BAA10g08930 A10 10929025 G A intergenic_region MODIFIER n.10929025G>A| S267
113519 BAA10g08930 A10 10941137 C T missense_variant MODERATE c.461G>A|p.Gly154Glu S84
S93
113520 BAA10g08930 A10 10941183 G A intron_variant MODIFIER c.427-12C>T| S286
113521 BAA10g08930 A10 10941727 G A synonymous_variant LOW c.366C>T|p.Arg122Arg S267
113522 BAA10g08930 A10 10941780 C T missense_variant MODERATE c.313G>A|p.Ala105Thr S44
113523 BAA10g08930 A10 10943579 C A upstream_gene_variant MODIFIER c.-1487G>T| S288
113524 BAA10g08930 A10 10944334 G A upstream_gene_variant MODIFIER c.-2242C>T| S296
113525 BAA10g08930 A10 10944969 C T upstream_gene_variant MODIFIER c.-2877G>A| S255