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
82601 BAA01g43860 A01 29042387 G A upstream_gene_variant MODIFIER c.-2154C>T| S129
82602 BAA01g43860 A01 29042469 C T upstream_gene_variant MODIFIER c.-2236G>A| S216
82603 BAA01g43860 A01 29045062 C T upstream_gene_variant MODIFIER c.-4829G>A| S208
S93
82604 BAA01g43870 A01 29045689 G A missense_variant MODERATE c.637C>T|p.Pro213Ser S143
82605 BAA01g43870 A01 29045882 C T synonymous_variant LOW c.444G>A|p.Ala148Ala S35
82606 BAA01g43870 A01 29046146 G A synonymous_variant LOW c.180C>T|p.Thr60Thr S143
82607 BAA01g43870 A01 29048903 G A upstream_gene_variant MODIFIER c.-2578C>T| S293
82608 BAA01g43870 A01 29049053 G A upstream_gene_variant MODIFIER c.-2728C>T| S143
82609 BAA01g43880 A01 29051590 G A upstream_gene_variant MODIFIER c.-254G>A| S259
82610 BAA01g43880 A01 29051883 C T missense_variant MODERATE c.40C>T|p.Leu14Phe S206
S26
82611 BAA01g43880 A01 29052175 C T missense_variant MODERATE c.332C>T|p.Ser111Phe S170
82612 BAA01g43880 A01 29052583 G A missense_variant MODERATE c.400G>A|p.Asp134Asn S244
82613 BAA01g43880 A01 29053117 C T synonymous_variant LOW c.934C>T|p.Leu312Leu S182
82614 BAA01g43880 A01 29053842 C T downstream_gene_variant MODIFIER c.*603C>T| S256
82615 BAA01g43880 A01 29054144 C T downstream_gene_variant MODIFIER c.*905C>T| S247
82616 BAA01g43890 A01 29054514 G A upstream_gene_variant MODIFIER c.-4772G>A| S169
82617 BAA01g43890 A01 29055213 C T upstream_gene_variant MODIFIER c.-4073C>T| S126
82618 BAA01g43890 A01 29057471 T C upstream_gene_variant MODIFIER c.-1815T>C| S163
82619 BAA01g43890 A01 29059794 G A synonymous_variant LOW c.360G>A|p.Gly120Gly S294
82620 BAA01g43890 A01 29059910 G A missense_variant MODERATE c.476G>A|p.Gly159Asp S36
82621 BAA01g43890 A01 29060495 C T splice_region_variant&intron_variant LOW c.626+4C>T| S146
82622 BAA01g43900 A01 29060973 C T upstream_gene_variant MODIFIER c.-1141C>T| S1
82623 BAA01g43890 A01 29061049 G A missense_variant MODERATE c.874G>A|p.Gly292Arg S87
82624 BAA01g43900 A01 29061938 G A upstream_gene_variant MODIFIER c.-176G>A| S138
82625 BAA01g43900 A01 29062269 G A stop_gained HIGH c.156G>A|p.Trp52* S229