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
10751 BAA01g08640 A01 3819317 G A missense_variant MODERATE c.1333G>A|p.Asp445Asn S281
10752 BAA01g08630 A01 3820123 C T downstream_gene_variant MODIFIER c.*3082C>T| S182
10753 BAA01g08650 A01 3820932 G A missense_variant MODERATE c.2878C>T|p.Leu960Phe S15
10754 BAA01g08630 A01 3821705 G A downstream_gene_variant MODIFIER c.*4664G>A| S95
10755 BAA01g08630 A01 3821756 C T downstream_gene_variant MODIFIER c.*4715C>T| S278
10756 BAA01g08640 A01 3824212 C T downstream_gene_variant MODIFIER c.*4407C>T| S185
10757 BAA01g08650 A01 3824815 G A missense_variant MODERATE c.830C>T|p.Ala277Val S262
10758 BAA01g08660 A01 3825312 C T downstream_gene_variant MODIFIER c.*3219G>A| S236
10759 BAA01g08650 A01 3825833 G A missense_variant MODERATE c.340C>T|p.Pro114Ser S259
10760 BAA01g08650 A01 3826276 C T upstream_gene_variant MODIFIER c.-104G>A| S136
10761 BAA01g08650 A01 3828521 G A upstream_gene_variant MODIFIER c.-2349C>T| S85
10762 BAA01g08660 A01 3828930 C T stop_gained HIGH c.1170G>A|p.Trp390* S100
10763 BAA01g08660 A01 3829193 G A missense_variant MODERATE c.907C>T|p.Pro303Ser S274
10764 BAA01g08660 A01 3829269 C T missense_variant MODERATE c.831G>A|p.Met277Ile S275
10765 BAA01g08660 A01 3829427 G A missense_variant MODERATE c.673C>T|p.Arg225Cys S190
10766 BAA01g08660 A01 3829515 G A synonymous_variant LOW c.585C>T|p.Phe195Phe S110
10767 BAA01g08660 A01 3829537 G A missense_variant MODERATE c.563C>T|p.Pro188Leu S229
10768 BAA01g08660 A01 3829714 G A missense_variant MODERATE c.386C>T|p.Pro129Leu S293
10769 BAA01g08660 A01 3830017 G A missense_variant MODERATE c.83C>T|p.Ser28Phe S207
10770 BAA01g08660 A01 3830074 G A missense_variant MODERATE c.26C>T|p.Pro9Leu S139
10771 BAA01g08650 A01 3830333 C T upstream_gene_variant MODIFIER c.-4161G>A| S118
10772 BAA01g08650 A01 3830986 C T upstream_gene_variant MODIFIER c.-4814G>A| S206
S26
10773 BAA01g08660 A01 3832671 C T upstream_gene_variant MODIFIER c.-2572G>A| S218
10774 BAA01g08660 A01 3833309 G A upstream_gene_variant MODIFIER c.-3210C>T| S202
10775 BAA01g08670 A01 3834400 G A missense_variant MODERATE c.587G>A|p.Gly196Glu S172
S217