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
42601 BAA01g26340 A01 14661371 G A downstream_gene_variant MODIFIER c.*3131G>A| S188
42602 BAA01g26340 A01 14662097 G A downstream_gene_variant MODIFIER c.*3857G>A| S63
42603 BAA01g26340 A01 14662347 C T downstream_gene_variant MODIFIER c.*4107C>T| S134
S259
42604 BAA01g26340 A01 14662841 A T downstream_gene_variant MODIFIER c.*4601A>T| S270
S92
42605 BAA01g26340 A01 14663158 C T downstream_gene_variant MODIFIER c.*4918C>T| S117
42606 BAA01g26350 A01 14663678 G A missense_variant MODERATE c.2438C>T|p.Thr813Ile S245
42607 BAA01g26350 A01 14663851 C T intron_variant MODIFIER c.2335-70G>A| S183
42608 BAA01g26350 A01 14664102 G A synonymous_variant LOW c.2280C>T|p.Ser760Ser S14
42609 BAA01g26350 A01 14666658 G A synonymous_variant LOW c.753C>T|p.Phe251Phe S299
42610 BAA01g26350 A01 14666990 C T missense_variant MODERATE c.626G>A|p.Cys209Tyr S96
42611 BAA01g26350 A01 14667840 C T synonymous_variant LOW c.33G>A|p.Thr11Thr S296
42612 BAA01g26350 A01 14667899 C T upstream_gene_variant MODIFIER c.-27G>A| S150
42613 BAA01g26350 A01 14667913 C T upstream_gene_variant MODIFIER c.-41G>A| S177
42614 BAA01g26350 A01 14667979 C T upstream_gene_variant MODIFIER c.-107G>A| S182
42615 BAA01g26350 A01 14668640 G A upstream_gene_variant MODIFIER c.-768C>T| S1
S161
S90
42616 BAA01g26350 A01 14668643 G A upstream_gene_variant MODIFIER c.-771C>T| S187
42617 BAA01g26350 A01 14669177 C T upstream_gene_variant MODIFIER c.-1305G>A| S97
42618 BAA01g26350 A01 14669436 G A upstream_gene_variant MODIFIER c.-1564C>T| S110
42619 BAA01g26350 A01 14669649 G A upstream_gene_variant MODIFIER c.-1777C>T| S298
42620 BAA01g26350 A01 14670249 G A upstream_gene_variant MODIFIER c.-2377C>T| S236
42621 BAA01g26350 A01 14670299 C T upstream_gene_variant MODIFIER c.-2427G>A| S134
42622 BAA01g26360 A01 14671323 C T missense_variant MODERATE c.2644G>A|p.Gly882Ser S25
42623 BAA01g26360 A01 14671660 C T missense_variant MODERATE c.2588G>A|p.Ser863Asn S295
42624 BAA01g26360 A01 14672279 G A synonymous_variant LOW c.2256C>T|p.Asn752Asn S96
42625 BAA01g26360 A01 14672724 C T missense_variant MODERATE c.2039G>A|p.Arg680Lys S273