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
160701 BAA02g07860 A02 3386472 C T missense_variant MODERATE c.616G>A|p.Glu206Lys S203
S273
S68
160702 BAA02g07860 A02 3386558 G A missense_variant MODERATE c.530C>T|p.Ser177Phe S169
160703 BAA02g07860 A02 3387499 C T upstream_gene_variant MODIFIER c.-236G>A| S257
160704 BAA02g07860 A02 3388144 G A upstream_gene_variant MODIFIER c.-881C>T| S82
S92
160705 BAA02g07870 A02 3388786 G A missense_variant MODERATE c.1442C>T|p.Ala481Val S95
160706 BAA02g07860 A02 3390680 C T upstream_gene_variant MODIFIER c.-3417G>A| S16
160707 BAA02g07880 A02 3391317 C T missense_variant MODERATE c.2314G>A|p.Asp772Asn S287
160708 BAA02g07880 A02 3392783 C T missense_variant MODERATE c.1105G>A|p.Gly369Arg S46
160709 BAA02g07880 A02 3393167 G A missense_variant MODERATE c.721C>T|p.Leu241Phe S174
160710 BAA02g07880 A02 3393236 C T missense_variant MODERATE c.652G>A|p.Gly218Ser S15
S3
160711 BAA02g07880 A02 3393280 G A missense_variant MODERATE c.608C>T|p.Thr203Ile S50
160712 BAA02g07870 A02 3393515 C T upstream_gene_variant MODIFIER c.-2909G>A| S94
160713 BAA02g07880 A02 3393679 G A synonymous_variant LOW c.444C>T|p.Ala148Ala S105
S106
160714 BAA02g07880 A02 3393821 G A missense_variant MODERATE c.302C>T|p.Pro101Leu S158
160715 BAA02g07880 A02 3393889 C T synonymous_variant LOW c.234G>A|p.Ser78Ser S206
160716 BAA02g07880 A02 3394096 C T synonymous_variant LOW c.27G>A|p.Arg9Arg S174
S216
S265
S39
160717 BAA02g07870 A02 3394946 C T upstream_gene_variant MODIFIER c.-4340G>A| S299
160718 BAA02g07880 A02 3395613 G A upstream_gene_variant MODIFIER c.-1491C>T| S202
160719 BAA02g07890 A02 3396378 C T missense_variant MODERATE c.2588G>A|p.Arg863His S212
160720 BAA02g07890 A02 3396467 G A synonymous_variant LOW c.2499C>T|p.Phe833Phe S282
160721 BAA02g07880 A02 3398112 G A upstream_gene_variant MODIFIER c.-3990C>T| S244
160722 BAA02g07890 A02 3399434 C T splice_donor_variant&intron_variant HIGH c.1437+1G>A| S42
160723 BAA02g07890 A02 3400328 C T missense_variant MODERATE c.544G>A|p.Asp182Asn S6
160724 BAA02g07900 A02 3401454 C T downstream_gene_variant MODIFIER c.*2503G>A| S76
160725 BAA02g07890 A02 3401714 G A missense_variant MODERATE c.377C>T|p.Ala126Val S271