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
84751 BAA01g44890 A01 29892667 C T downstream_gene_variant MODIFIER c.*1960G>A| S186
84752 BAA01g44890 A01 29892741 G A downstream_gene_variant MODIFIER c.*1886C>T| S176
84753 BAA01g44890 A01 29893115 C T downstream_gene_variant MODIFIER c.*1512G>A| S63
84754 BAA01g44890 A01 29894636 G A synonymous_variant LOW c.594C>T|p.Phe198Phe S265
84755 BAA01g44890 A01 29894802 G A missense_variant MODERATE c.428C>T|p.Pro143Leu S135
S68
84756 BAA01g44890 A01 29895457 C T missense_variant MODERATE c.92G>A|p.Gly31Glu S161
84757 BAA01g44890 A01 29895870 G A upstream_gene_variant MODIFIER c.-233C>T| S151
84758 BAA01g44890 A01 29896294 G A upstream_gene_variant MODIFIER c.-657C>T| S262
84759 BAA01g44890 A01 29897624 G A upstream_gene_variant MODIFIER c.-1987C>T| S202
84760 BAA01g44900 A01 29902333 C T intron_variant MODIFIER c.182+1719C>T| S234
84761 BAA01g44910 A01 29903828 G A upstream_gene_variant MODIFIER c.-4996G>A| S105
S106
84762 BAA01g44900 A01 29904793 C T missense_variant MODERATE c.233C>T|p.Ser78Phe S232
84763 BAA01g44900 A01 29904807 G A missense_variant MODERATE c.247G>A|p.Gly83Arg S61
84764 BAA01g44900 A01 29905351 C T missense_variant MODERATE c.593C>T|p.Ser198Phe S69
84765 BAA01g44910 A01 29906076 C T upstream_gene_variant MODIFIER c.-2748C>T| S223
84766 BAA01g44910 A01 29906448 G A upstream_gene_variant MODIFIER c.-2376G>A| S293
84767 BAA01g44910 A01 29907104 G A upstream_gene_variant MODIFIER c.-1720G>A| S151
84768 BAA01g44910 A01 29907412 C T upstream_gene_variant MODIFIER c.-1412C>T| S52
84769 BAA01g44910 A01 29908531 C T upstream_gene_variant MODIFIER c.-293C>T| S305
84770 BAA01g44910 A01 29908534 G A upstream_gene_variant MODIFIER c.-290G>A| S117
84771 BAA01g44900 A01 29909490 C T downstream_gene_variant MODIFIER c.*3435C>T| S171
84772 BAA01g44900 A01 29910130 G A downstream_gene_variant MODIFIER c.*4075G>A| S247
84773 BAA01g44930 A01 29910921 C T upstream_gene_variant MODIFIER c.-4441C>T| S267
84774 BAA01g44920 A01 29914093 G A upstream_gene_variant MODIFIER c.-111C>T| S276
84775 BAA01g44920 A01 29914753 C T upstream_gene_variant MODIFIER c.-771G>A| S134