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
192951 BAA02g27200 A02 15255370 G A missense_variant MODERATE c.1774C>T|p.Pro592Ser S161
192952 BAA02g27200 A02 15255750 C T missense_variant MODERATE c.1394G>A|p.Arg465His S107
192953 BAA02g27210 A02 15256143 C T upstream_gene_variant MODIFIER c.-3940C>T| S14
192954 BAA02g27200 A02 15257000 C T missense_variant MODERATE c.436G>A|p.Asp146Asn S139
192955 BAA02g27200 A02 15257185 G A missense_variant MODERATE c.251C>T|p.Ser84Phe S188
192956 BAA02g27200 A02 15257930 G A upstream_gene_variant MODIFIER c.-414C>T| S294
192957 BAA02g27200 A02 15258270 C T upstream_gene_variant MODIFIER c.-754G>A| S42
192958 BAA02g27200 A02 15259232 G A upstream_gene_variant MODIFIER c.-1716C>T| S239
192959 BAA02g27200 A02 15259322 G A upstream_gene_variant MODIFIER c.-1806C>T| S35
192960 BAA02g27200 A02 15259833 G A upstream_gene_variant MODIFIER c.-2317C>T| S56
192961 BAA02g27200 A02 15261264 G A upstream_gene_variant MODIFIER c.-3748C>T| S139
192962 BAA02g27200 A02 15261281 G A upstream_gene_variant MODIFIER c.-3765C>T| S155
S211
192963 BAA02g27200 A02 15261320 C T upstream_gene_variant MODIFIER c.-3804G>A| S2
192964 BAA02g27200 A02 15261584 C T upstream_gene_variant MODIFIER c.-4068G>A| S179
192965 BAA02g27220 A02 15265658 C T missense_variant MODERATE c.1042C>T|p.Pro348Ser S193
192966 BAA02g27220 A02 15265873 G A missense_variant MODERATE c.1192G>A|p.Asp398Asn S139
192967 BAA02g27220 A02 15265903 G A missense_variant MODERATE c.1222G>A|p.Val408Ile S38
192968 BAA02g27230 A02 15267438 C T upstream_gene_variant MODIFIER c.-1699C>T| S276
192969 BAA02g27230 A02 15267864 C T upstream_gene_variant MODIFIER c.-1273C>T| S18
192970 BAA02g27230 A02 15268459 G A upstream_gene_variant MODIFIER c.-678G>A| S237
192971 BAA02g27230 A02 15268683 G A upstream_gene_variant MODIFIER c.-454G>A| S302
192972 BAA02g27230 A02 15268716 G A upstream_gene_variant MODIFIER c.-421G>A| S303
192973 BAA02g27230 A02 15269185 G A missense_variant MODERATE c.49G>A|p.Ala17Thr S251
192974 BAA02g27230 A02 15271444 C T downstream_gene_variant MODIFIER c.*532C>T| S124
192975 BAA02g27230 A02 15271751 G A downstream_gene_variant MODIFIER c.*839G>A| S10