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
163201 BAA02g10010 A02 4421927 G A upstream_gene_variant MODIFIER c.-186C>T| S203
163202 BAA02g10010 A02 4422990 G A upstream_gene_variant MODIFIER c.-1249C>T| S203
163203 BAA02g10010 A02 4425891 C T upstream_gene_variant MODIFIER c.-4150G>A| S182
163204 BAA02g10010 A02 4426480 G A upstream_gene_variant MODIFIER c.-4739C>T| S132
S137
S215
S89
163205 BAA02g10010 A02 4426563 C T upstream_gene_variant MODIFIER c.-4822G>A| S100
163206 BAA02g10010 A02 4426625 C T upstream_gene_variant MODIFIER c.-4884G>A| S131
163207 BAA02g10020 A02 4426932 G A upstream_gene_variant MODIFIER c.-2720C>T| S187
163208 BAA02g10020 A02 4426936 C T upstream_gene_variant MODIFIER c.-2724G>A| S83
S88
163209 BAA02g10030 A02 4427184 G A synonymous_variant LOW c.135G>A|p.Lys45Lys S298
163210 BAA02g10020 A02 4427580 C T upstream_gene_variant MODIFIER c.-3368G>A| S33
163211 BAA02g10030 A02 4427736 C T missense_variant MODERATE c.470C>T|p.Ser157Phe S204
163212 BAA02g10020 A02 4427924 C T upstream_gene_variant MODIFIER c.-3712G>A| S90
163213 BAA02g10020 A02 4429103 C T upstream_gene_variant MODIFIER c.-4891G>A| S238
163214 BAA02g10040 A02 4429423 C T missense_variant MODERATE c.505G>A|p.Asp169Asn S78
S83
163215 BAA02g10040 A02 4429493 G A synonymous_variant LOW c.435C>T|p.Phe145Phe S85
163216 BAA02g10040 A02 4431298 G A upstream_gene_variant MODIFIER c.-242C>T| S209
163217 BAA02g10040 A02 4431827 G A upstream_gene_variant MODIFIER c.-771C>T| S225
163218 BAA02g10050 A02 4433108 G A synonymous_variant LOW c.24G>A|p.Ala8Ala S110
163219 BAA02g10050 A02 4433472 G A synonymous_variant LOW c.285G>A|p.Gln95Gln S259
163220 BAA02g10050 A02 4433584 G A missense_variant MODERATE c.397G>A|p.Asp133Asn S61
163221 BAA02g10050 A02 4434256 G A synonymous_variant LOW c.831G>A|p.Gln277Gln S60
163222 BAA02g10050 A02 4434686 C T missense_variant MODERATE c.1105C>T|p.Arg369Cys S71
163223 BAA02g10040 A02 4434983 G A upstream_gene_variant MODIFIER c.-3927C>T| S191
163224 BAA02g10050 A02 4435258 G A splice_donor_variant&intron_variant HIGH c.1416+1G>A| S43
163225 BAA02g10050 A02 4435450 G A splice_region_variant&intron_variant LOW c.1530+5G>A| S35