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
86451 BAA01g45970 A01 30622034 C T downstream_gene_variant MODIFIER c.*2C>T| S174
86452 BAA01g45970 A01 30623385 G T downstream_gene_variant MODIFIER c.*1353G>T| S95
86453 BAA01g45970 A01 30623870 C T downstream_gene_variant MODIFIER c.*1838C>T| S1
S90
86454 BAA01g45970 A01 30624119 C T downstream_gene_variant MODIFIER c.*2087C>T| S118
86455 BAA01g45970 A01 30624372 G A downstream_gene_variant MODIFIER c.*2340G>A|
86456 BAA01g45970 A01 30625273 C T downstream_gene_variant MODIFIER c.*3241C>T| S240
86457 BAA01g45970 A01 30625286 G A downstream_gene_variant MODIFIER c.*3254G>A| S202
86458 BAA01g45980 A01 30626090 C T synonymous_variant LOW c.1305G>A|p.Lys435Lys S47
86459 BAA01g45990 A01 30627115 T C upstream_gene_variant MODIFIER c.-3349T>C| S190
86460 BAA01g45990 A01 30627245 C T upstream_gene_variant MODIFIER c.-3219C>T| S183
S198
86461 BAA01g45980 A01 30627563 C T synonymous_variant LOW c.540G>A|p.Ala180Ala S201
86462 BAA01g45980 A01 30627835 C T splice_donor_variant&intron_variant HIGH c.430+1G>A| S148
S210
S30
S31
86463 BAA01g45980 A01 30628080 C T missense_variant&splice_region_variant MODERATE c.277G>A|p.Glu93Lys S54
86464 BAA01g45980 A01 30629093 G A upstream_gene_variant MODIFIER c.-123C>T| S151
86465 BAA01g45980 A01 30629754 G A upstream_gene_variant MODIFIER c.-784C>T| S57
86466 BAA01g45980 A01 30631824 C T upstream_gene_variant MODIFIER c.-2854G>A| S221
86467 BAA01g45980 A01 30632734 G A upstream_gene_variant MODIFIER c.-3764C>T| S43
86468 BAA01g45980 A01 30633269 C T upstream_gene_variant MODIFIER c.-4299G>A| S205
86469 BAA01g45990 A01 30634447 G A downstream_gene_variant MODIFIER c.*2089G>A| S158
86470 BAA01g46010 A01 30637693 C T upstream_gene_variant MODIFIER c.-1768C>T| S261
86471 BAA01g46010 A01 30639218 C T upstream_gene_variant MODIFIER c.-243C>T| S37
86472 BAA01g46010 A01 30639862 G A stop_gained HIGH c.402G>A|p.Trp134* S179
86473 BAA01g46010 A01 30639886 G A synonymous_variant LOW c.426G>A|p.Val142Val S295
86474 BAA01g46010 A01 30640255 C T intron_variant MODIFIER c.623+11C>T| S182
86475 BAA01g46010 A01 30640647 G A synonymous_variant LOW c.840G>A|p.Glu280Glu S99