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
78601 BAA01g41320 A01 27481867 C T upstream_gene_variant MODIFIER c.-1969G>A| S239
78602 BAA01g41320 A01 27482041 G A upstream_gene_variant MODIFIER c.-2143C>T| S33
S70
78603 BAA01g41320 A01 27482696 G A upstream_gene_variant MODIFIER c.-2798C>T| S20
78604 BAA01g41320 A01 27482794 G A upstream_gene_variant MODIFIER c.-2896C>T| S259
78605 BAA01g41330 A01 27483070 C T missense_variant MODERATE c.775G>A|p.Glu259Lys S131
78606 BAA01g41330 A01 27483295 C T missense_variant MODERATE c.640G>A|p.Glu214Lys S17
78607 BAA01g41320 A01 27484626 C T upstream_gene_variant MODIFIER c.-4728G>A| S251
78608 BAA01g41330 A01 27485260 G A upstream_gene_variant MODIFIER c.-958C>T| S297
78609 BAA01g41330 A01 27485364 G A upstream_gene_variant MODIFIER c.-1062C>T| S36
78610 BAA01g41330 A01 27486236 C T upstream_gene_variant MODIFIER c.-1934G>A| S251
78611 BAA01g41340 A01 27486397 G A missense_variant MODERATE c.91G>A|p.Glu31Lys S245
78612 BAA01g41340 A01 27486434 C T missense_variant MODERATE c.128C>T|p.Ser43Phe S186
78613 BAA01g41350 A01 27487354 C T missense_variant MODERATE c.1925G>A|p.Arg642Lys S136
78614 BAA01g41350 A01 27489010 C T synonymous_variant LOW c.1179G>A|p.Lys393Lys S62
78615 BAA01g41340 A01 27489493 C T downstream_gene_variant MODIFIER c.*2599C>T| S37
78616 BAA01g41340 A01 27491153 G A downstream_gene_variant MODIFIER c.*4259G>A| S268
78617 BAA01g41360 A01 27492200 C T downstream_gene_variant MODIFIER c.*3299G>A| S279
78618 BAA01g41350 A01 27495110 G A upstream_gene_variant MODIFIER c.-1711C>T| S308
78619 BAA01g41360 A01 27495849 G A missense_variant MODERATE c.559C>T|p.Pro187Ser S86
78620 BAA01g41360 A01 27500275 C T upstream_gene_variant MODIFIER c.-3868G>A| S266
78621 BAA01g41370 A01 27501703 C T downstream_gene_variant MODIFIER c.*1035G>A| S190
78622 BAA01g41370 A01 27503439 C T intron_variant MODIFIER c.1817-466G>A| S16
78623 BAA01g41370 A01 27503494 G A intron_variant MODIFIER c.1817-521C>T| S86
78624 BAA01g41370 A01 27503749 C T intron_variant MODIFIER c.1817-776G>A| S205
78625 BAA01g41370 A01 27504021 C T intron_variant MODIFIER c.1817-1048G>A| S241