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
13651 BAA01g10690 A01 4911290 C T upstream_gene_variant MODIFIER c.-2984C>T| S305
13652 BAA01g10680 A01 4912193 G A splice_acceptor_variant&intron_variant HIGH c.928-1G>A| S159
S243
13653 BAA01g10680 A01 4912327 G A missense_variant MODERATE c.1061G>A|p.Gly354Asp S33
13654 BAA01g10680 A01 4912929 C T synonymous_variant LOW c.1402C>T|p.Leu468Leu S53
13655 BAA01g10690 A01 4913858 C T upstream_gene_variant MODIFIER c.-416C>T| S303
13656 BAA01g10690 A01 4914789 G A splice_region_variant&stop_retained_variant LOW c.516G>A|p.Ter172Ter S177
13657 BAA01g10700 A01 4915844 G A missense_variant MODERATE c.1139C>T|p.Thr380Met S45
13658 BAA01g10680 A01 4916806 G A downstream_gene_variant MODIFIER c.*3010G>A| S162
13659 BAA01g10700 A01 4916964 G A missense_variant MODERATE c.398C>T|p.Ser133Phe S195
13660 BAA01g10700 A01 4917004 C T missense_variant MODERATE c.358G>A|p.Gly120Arg S44
13661 BAA01g10700 A01 4917109 C T missense_variant MODERATE c.253G>A|p.Val85Ile S210
S225
13662 BAA01g10680 A01 4917417 C T downstream_gene_variant MODIFIER c.*3621C>T| S42
13663 BAA01g10700 A01 4917496 G A synonymous_variant LOW c.63C>T|p.Leu21Leu S297
13664 BAA01g10700 A01 4920841 G A upstream_gene_variant MODIFIER c.-3283C>T| S149
13665 BAA01g10700 A01 4921836 G A upstream_gene_variant MODIFIER c.-4278C>T| S13
13666 BAA01g10700 A01 4922040 G A upstream_gene_variant MODIFIER c.-4482C>T| S9
13667 BAA01g10710 A01 4923543 G A upstream_gene_variant MODIFIER c.-4382G>A| S95
13668 BAA01g10710 A01 4927996 G A synonymous_variant LOW c.72G>A|p.Gln24Gln S201
13669 BAA01g10710 A01 4928012 G A missense_variant MODERATE c.88G>A|p.Asp30Asn S232
13670 BAA01g10710 A01 4928053 G A synonymous_variant LOW c.129G>A|p.Pro43Pro S95
13671 BAA01g10710 A01 4928100 C T missense_variant MODERATE c.176C>T|p.Ser59Phe S157
S166
S167
S262
S263
13672 BAA01g10710 A01 4928153 C T synonymous_variant LOW c.229C>T|p.Leu77Leu S268
13673 BAA01g10710 A01 4928238 G A intron_variant MODIFIER c.288+26G>A| S204
13674 BAA01g10710 A01 4928518 G A missense_variant MODERATE c.493G>A|p.Glu165Lys S73
S91
13675 BAA01g10710 A01 4929002 C T intron_variant MODIFIER c.609+368C>T| S90