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
127401 BAA10g15830 A10 16024306 G A upstream_gene_variant MODIFIER c.-3845C>T| S129
127402 BAA10g15830 A10 16024425 G A upstream_gene_variant MODIFIER c.-3964C>T| S125
127403 BAA10g15830 A10 16024513 G T upstream_gene_variant MODIFIER c.-4052C>A| S53
127404 BAA10g15870 A10 16026149 C T missense_variant MODERATE c.1166G>A|p.Gly389Glu S232
127405 BAA10g15870 A10 16026567 G A missense_variant MODERATE c.748C>T|p.Leu250Phe S292
127406 BAA10g15870 A10 16026951 G A synonymous_variant LOW c.364C>T|p.Leu122Leu S35
127407 BAA10g15870 A10 16027833 C T missense_variant MODERATE c.175G>A|p.Glu59Lys S135
127408 BAA10g15850 A10 16028237 G A upstream_gene_variant MODIFIER c.-4849C>T| S286
127409 BAA10g15860 A10 16028991 C T upstream_gene_variant MODIFIER c.-3145G>A| S23
127410 BAA10g15860 A10 16030318 G A upstream_gene_variant MODIFIER c.-4472C>T| S164
127411 BAA10g15860 A10 16030370 C T upstream_gene_variant MODIFIER c.-4524G>A| S116
127412 BAA10g15860 A10 16030447 C T upstream_gene_variant MODIFIER c.-4601G>A| S161
127413 BAA10g15880 A10 16030886 G A synonymous_variant LOW c.78G>A|p.Leu26Leu S197
127414 BAA10g15880 A10 16031993 G A missense_variant MODERATE c.386G>A|p.Ser129Asn S67
127415 BAA10g15880 A10 16032244 G A synonymous_variant LOW c.543G>A|p.Gly181Gly S65
127416 BAA10g15870 A10 16032904 G A upstream_gene_variant MODIFIER c.-4897C>T| S234
127417 BAA10g15890 A10 16034556 G A upstream_gene_variant MODIFIER c.-4014G>A| S209
127418 BAA10g15880 A10 16035048 G A synonymous_variant LOW c.1491G>A|p.Gln497Gln S293
127419 BAA10g15890 A10 16035585 G A upstream_gene_variant MODIFIER c.-2985G>A| S165
127420 BAA10g15880 A10 16036145 G A synonymous_variant LOW c.1950G>A|p.Arg650Arg S18
127421 BAA10g15890 A10 16036526 G A upstream_gene_variant MODIFIER c.-2044G>A| S9
127422 BAA10g15890 A10 16036708 C T upstream_gene_variant MODIFIER c.-1862C>T| S13
127423 BAA10g15880 A10 16036958 C T missense_variant MODERATE c.2203C>T|p.Leu735Phe S200
S274
S303
127424 BAA10g15890 A10 16036997 C T upstream_gene_variant MODIFIER c.-1573C>T| S8
127425 BAA10g15890 A10 16037534 G A upstream_gene_variant MODIFIER c.-1036G>A| S25