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
76601 BAA01g40470 A01 26815356 C T synonymous_variant LOW c.2958G>A|p.Gln986Gln S89
76602 BAA01g40470 A01 26815948 C T missense_variant MODERATE c.2575G>A|p.Glu859Lys S90
76603 BAA01g40470 A01 26816555 A C missense_variant MODERATE c.1968T>G|p.His656Gln S46
76604 BAA01g40470 A01 26816825 A G synonymous_variant LOW c.1698T>C|p.Val566Val S28
76605 BAA01g40470 A01 26816892 C T missense_variant MODERATE c.1631G>A|p.Arg544Lys S298
76606 BAA01g40470 A01 26816969 C T synonymous_variant LOW c.1554G>A|p.Gln518Gln S294
S79
76607 BAA01g40470 A01 26817451 G A synonymous_variant LOW c.1072C>T|p.Leu358Leu S255
76608 BAA01g40470 A01 26818305 C T stop_gained HIGH c.396G>A|p.Trp132* S166
76609 BAA01g40470 A01 26819211 C T upstream_gene_variant MODIFIER c.-79G>A| S115
76610 BAA01g40470 A01 26819787 C T upstream_gene_variant MODIFIER c.-655G>A| S65
76611 BAA01g40470 A01 26819795 G A upstream_gene_variant MODIFIER c.-663C>T| S20
76612 BAA01g40470 A01 26819920 G A upstream_gene_variant MODIFIER c.-788C>T| S212
76613 BAA01g40470 A01 26820313 C T upstream_gene_variant MODIFIER c.-1181G>A| S198
76614 BAA01g40470 A01 26820721 G A upstream_gene_variant MODIFIER c.-1589C>T| S190
76615 BAA01g40470 A01 26821204 C T upstream_gene_variant MODIFIER c.-2072G>A| S92
76616 BAA01g40470 A01 26821729 C T upstream_gene_variant MODIFIER c.-2597G>A| S167
76617 BAA01g40480 A01 26822834 G A synonymous_variant LOW c.237C>T|p.Pro79Pro S150
S202
76618 BAA01g40470 A01 26823349 C T upstream_gene_variant MODIFIER c.-4217G>A| S120
76619 BAA01g40490 A01 26823884 C T missense_variant MODERATE c.422C>T|p.Pro141Leu S210
76620 BAA01g40480 A01 26824217 G A upstream_gene_variant MODIFIER c.-1147C>T| S84
S93
76621 BAA01g40480 A01 26824407 G A upstream_gene_variant MODIFIER c.-1337C>T| S110
76622 BAA01g40500 A01 26825115 C T synonymous_variant LOW c.207C>T|p.Leu69Leu S115
76623 BAA01g40500 A01 26825499 C T missense_variant MODERATE c.512C>T|p.Ser171Phe S135
S262
76624 BAA01g40480 A01 26825847 C T upstream_gene_variant MODIFIER c.-2777G>A| S19
76625 BAA01g40500 A01 26825917 G A missense_variant MODERATE c.596G>A|p.Gly199Glu S121