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
200701 BAA02g30480 A02 17873551 G A missense_variant MODERATE c.3014G>A|p.Arg1005Lys S81
S85
200702 BAA02g30480 A02 17874366 G A downstream_gene_variant MODIFIER c.*787G>A| S174
S216
200703 BAA02g30480 A02 17874961 C T downstream_gene_variant MODIFIER c.*1382C>T| S270
200704 BAA02g30480 A02 17876811 C T downstream_gene_variant MODIFIER c.*3232C>T| S18
200705 BAA02g30500 A02 17879095 C T missense_variant MODERATE c.562G>A|p.Glu188Lys S168
S219
S278
S72
200706 BAA02g30500 A02 17879277 G A missense_variant MODERATE c.470C>T|p.Ser157Phe S59
200707 BAA02g30490 A02 17879945 C T downstream_gene_variant MODIFIER c.*4878C>T| S142
200708 BAA02g30490 A02 17880063 C T downstream_gene_variant MODIFIER c.*4996C>T| S92
200709 BAA02g30500 A02 17880868 C T upstream_gene_variant MODIFIER c.-654G>A| S121
200710 BAA02g30500 A02 17881095 G A upstream_gene_variant MODIFIER c.-881C>T| S232
200711 BAA02g30500 A02 17881437 G A upstream_gene_variant MODIFIER c.-1223C>T| S111
200712 BAA02g30500 A02 17881791 C T upstream_gene_variant MODIFIER c.-1577G>A| S135
200713 BAA02g30510 A02 17882014 C T synonymous_variant LOW c.639G>A|p.Leu213Leu S264
200714 BAA02g30510 A02 17882243 A G missense_variant MODERATE c.410T>C|p.Val137Ala S80
200715 BAA02g30510 A02 17882277 G A missense_variant MODERATE c.376C>T|p.Pro126Ser S278
200716 BAA02g30510 A02 17882522 C T missense_variant MODERATE c.230G>A|p.Arg77Lys
200717 BAA02g30500 A02 17883197 G A upstream_gene_variant MODIFIER c.-2983C>T| S217
S248
200718 BAA02g30500 A02 17883206 G A upstream_gene_variant MODIFIER c.-2992C>T| S217
S248
200719 BAA02g30500 A02 17883257 G A upstream_gene_variant MODIFIER c.-3043C>T| S274
S302
200720 BAA02g30510 A02 17883530 C T missense_variant MODERATE c.139G>A|p.Glu47Lys S87
200721 BAA02g30500 A02 17883630 C T upstream_gene_variant MODIFIER c.-3416G>A| S273
200722 BAA02g30500 A02 17884766 C T upstream_gene_variant MODIFIER c.-4552G>A| S183
S198
200723 BAA02g30500 A02 17884787 G A upstream_gene_variant MODIFIER c.-4573C>T| S153
S213
200724 BAA02g30500 A02 17885199 C T upstream_gene_variant MODIFIER c.-4985G>A| S178
200725 BAA02g30510 A02 17885470 C T intron_variant MODIFIER c.39+805G>A| S15
S3