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
61001 BAA01g32390 A01 21333921 G A downstream_gene_variant MODIFIER c.*4439G>A| S103
61002 BAA01g32400 A01 21336577 C T missense_variant MODERATE c.1052C>T|p.Ser351Phe S11
61003 BAA01g32400 A01 21337414 C T downstream_gene_variant MODIFIER c.*286C>T| S204
61004 BAA01g32400 A01 21337538 C T downstream_gene_variant MODIFIER c.*410C>T| S44
61005 BAA01g32400 A01 21337567 C T downstream_gene_variant MODIFIER c.*439C>T| S46
61006 BAA01g32400 A01 21337612 G A downstream_gene_variant MODIFIER c.*484G>A| S218
61007 BAA01g32400 A01 21338833 C T downstream_gene_variant MODIFIER c.*1705C>T| S148
S266
61008 BAA01g32400 A01 21339436 C T downstream_gene_variant MODIFIER c.*2308C>T| S249
61009 BAA01g32410 A01 21345526 C T upstream_gene_variant MODIFIER c.-1538G>A| S81
S85
61010 BAA01g32410 A01 21345910 G A upstream_gene_variant MODIFIER c.-1922C>T| S238
61011 BAA01g32410 A01 21346127 C T upstream_gene_variant MODIFIER c.-2139G>A| S216
61012 BAA01g32410 A01 21346802 G A upstream_gene_variant MODIFIER c.-2814C>T| S188
61013 BAA01g32410 A01 21348641 G A upstream_gene_variant MODIFIER c.-4653C>T| S202
61014 BAA01g32410 A01 21348685 G A upstream_gene_variant MODIFIER c.-4697C>T| S209
61015 BAA01g32420 A01 21349809 G A downstream_gene_variant MODIFIER c.*3503C>T| S124
61016 BAA01g32420 A01 21350221 C T downstream_gene_variant MODIFIER c.*3091G>A| S162
61017 BAA01g32420 A01 21350274 G A downstream_gene_variant MODIFIER c.*3038C>T| S151
61018 BAA01g32420 A01 21350988 C T downstream_gene_variant MODIFIER c.*2324G>A| S94
61019 BAA01g32420 A01 21351738 C T downstream_gene_variant MODIFIER c.*1574G>A| S242
61020 BAA01g32420 A01 21352148 G A downstream_gene_variant MODIFIER c.*1164C>T| S301
S304
61021 BAA01g32420 A01 21352802 C T downstream_gene_variant MODIFIER c.*510G>A| S54
61022 BAA01g32420 A01 21352822 G A downstream_gene_variant MODIFIER c.*490C>T| S187
61023 BAA01g32420 A01 21353659 G A intron_variant MODIFIER c.1194-42C>T| S12
61024 BAA01g32420 A01 21353987 C T missense_variant MODERATE c.994G>A|p.Glu332Lys S131
61025 BAA01g32420 A01 21355763 C T missense_variant MODERATE c.179G>A|p.Gly60Glu S211