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
161801 BAA02g08800 A02 3901941 C T missense_variant MODERATE c.1006G>A|p.Gly336Arg S167
161802 BAA02g08790 A02 3902010 G A upstream_gene_variant MODIFIER c.-2070C>T| S111
161803 BAA02g08800 A02 3902151 C T missense_variant MODERATE c.881G>A|p.Ser294Asn S274
161804 BAA02g08800 A02 3902405 G A missense_variant MODERATE c.716C>T|p.Pro239Leu S295
161805 BAA02g08800 A02 3902917 G A synonymous_variant LOW c.486C>T|p.Cys162Cys S105
S106
161806 BAA02g08790 A02 3903369 C T upstream_gene_variant MODIFIER c.-3429G>A| S179
161807 BAA02g08800 A02 3903826 G A splice_region_variant&intron_variant LOW c.162+7C>T| S293
161808 BAA02g08800 A02 3904074 C T missense_variant MODERATE c.4G>A|p.Asp2Asn S25
161809 BAA02g08810 A02 3904648 C T missense_variant MODERATE c.724G>A|p.Ala242Thr S18
161810 BAA02g08810 A02 3904851 G A missense_variant MODERATE c.521C>T|p.Ala174Val S35
161811 BAA02g08800 A02 3905297 G A upstream_gene_variant MODIFIER c.-1220C>T| S187
161812 BAA02g08800 A02 3905326 G A upstream_gene_variant MODIFIER c.-1249C>T| S119
161813 BAA02g08800 A02 3905632 G A upstream_gene_variant MODIFIER c.-1555C>T| S237
161814 BAA02g08800 A02 3906672 G A upstream_gene_variant MODIFIER c.-2595C>T| S156
161815 BAA02g08800 A02 3907380 G A upstream_gene_variant MODIFIER c.-3303C>T| S295
161816 BAA02g08820 A02 3907526 C T missense_variant MODERATE c.124C>T|p.Arg42Cys S128
161817 BAA02g08820 A02 3908431 C T missense_variant MODERATE c.626C>T|p.Ser209Phe S103
161818 BAA02g08820 A02 3909779 G A missense_variant MODERATE c.1325G>A|p.Gly442Glu S85
161819 BAA02g08810 A02 3910019 C T upstream_gene_variant MODIFIER c.-3987G>A| S1
161820 BAA02g08810 A02 3910054 G A upstream_gene_variant MODIFIER c.-4022C>T| S150
161821 BAA02g08830 A02 3911214 G A missense_variant MODERATE c.155C>T|p.Pro52Leu S36
161822 BAA02g08830 A02 3911897 G A upstream_gene_variant MODIFIER c.-449C>T| S125
161823 BAA02g08830 A02 3912530 T A upstream_gene_variant MODIFIER c.-1082A>T| S177
161824 BAA02g08830 A02 3912566 C T upstream_gene_variant MODIFIER c.-1118G>A| S40
S49
161825 BAA02g08830 A02 3913020 G A upstream_gene_variant MODIFIER c.-1572C>T| S162