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
85001 BAA01g45030 A01 30039615 G A downstream_gene_variant MODIFIER c.*4835G>A| S123
85002 BAA01g45030 A01 30039634 G A downstream_gene_variant MODIFIER c.*4854G>A| S158
85003 BAA01g45040 A01 30040295 G A downstream_gene_variant MODIFIER c.*723G>A| S61
85004 BAA01g45040 A01 30040496 C T downstream_gene_variant MODIFIER c.*924C>T| S57
85005 BAA01g45040 A01 30040725 C T downstream_gene_variant MODIFIER c.*1153C>T| S16
85006 BAA01g45050 A01 30040928 G A missense_variant MODERATE c.667C>T|p.Leu223Phe S246
85007 BAA01g45050 A01 30041081 C T missense_variant MODERATE c.582G>A|p.Met194Ile S166
85008 BAA01g45050 A01 30041448 G A synonymous_variant LOW c.312C>T|p.Thr104Thr S116
85009 BAA01g45050 A01 30041662 G A synonymous_variant LOW c.177C>T|p.Asn59Asn S228
85010 BAA01g45040 A01 30041742 C T downstream_gene_variant MODIFIER c.*2170C>T| S8
85011 BAA01g45050 A01 30043471 G A upstream_gene_variant MODIFIER c.-158C>T| S87
85012 BAA01g45050 A01 30043721 C T upstream_gene_variant MODIFIER c.-408G>A| S303
85013 BAA01g45050 A01 30043883 G A upstream_gene_variant MODIFIER c.-570C>T| S122
85014 BAA01g45060 A01 30044114 G A stop_gained HIGH c.3001C>T|p.Gln1001* S236
85015 BAA01g45060 A01 30044175 C T synonymous_variant LOW c.2940G>A|p.Thr980Thr S192
85016 BAA01g45060 A01 30044309 C T missense_variant MODERATE c.2906G>A|p.Cys969Tyr S239
85017 BAA01g45060 A01 30045662 C T missense_variant&splice_region_variant MODERATE c.1952G>A|p.Ser651Asn S92
85018 BAA01g45060 A01 30045796 C T synonymous_variant LOW c.1818G>A|p.Arg606Arg S279
85019 BAA01g45060 A01 30046371 G A splice_region_variant&intron_variant LOW c.1443+7C>T| S252
85020 BAA01g45060 A01 30046566 C T synonymous_variant LOW c.1332G>A|p.Gly444Gly S146
85021 BAA01g45060 A01 30047438 C T synonymous_variant LOW c.942G>A|p.Gly314Gly S12
85022 BAA01g45060 A01 30047491 C T missense_variant MODERATE c.889G>A|p.Ala297Thr S201
85023 BAA01g45060 A01 30047560 C T missense_variant MODERATE c.820G>A|p.Glu274Lys S251
85024 BAA01g45070 A01 30048550 C T upstream_gene_variant MODIFIER c.-2606C>T| S65
85025 BAA01g45060 A01 30049020 G A missense_variant MODERATE c.7C>T|p.Pro3Ser S250