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
33401 BAA01g22750 A01 11512623 G A upstream_gene_variant MODIFIER c.-4974C>T| S169
33402 BAA01g22760 A01 11512749 G A intron_variant MODIFIER c.1670+523C>T| S271
33403 BAA01g22760 A01 11512807 G A intron_variant MODIFIER c.1670+465C>T| S67
33404 BAA01g22760 A01 11513788 G A missense_variant MODERATE c.1373C>T|p.Ser458Phe S15
S3
33405 BAA01g22760 A01 11514212 C T missense_variant MODERATE c.1028G>A|p.Arg343Lys S182
33406 BAA01g22760 A01 11514396 C T splice_region_variant&intron_variant LOW c.912+4G>A| S184
33407 BAA01g22760 A01 11518705 C T upstream_gene_variant MODIFIER c.-2958G>A| S303
33408 BAA01g22770 A01 11520953 G A upstream_gene_variant MODIFIER c.-61C>T| S126
33409 BAA01g22770 A01 11521252 C T upstream_gene_variant MODIFIER c.-360G>A| S25
33410 BAA01g22780 A01 11521443 C T missense_variant MODERATE c.59C>T|p.Thr20Met S46
33411 BAA01g22780 A01 11521746 G A missense_variant MODERATE c.362G>A|p.Ser121Asn S195
33412 BAA01g22780 A01 11521992 G A missense_variant MODERATE c.608G>A|p.Arg203His S180
33413 BAA01g22780 A01 11522180 C T missense_variant MODERATE c.796C>T|p.Pro266Ser S289
S290
33414 BAA01g22780 A01 11522538 C T missense_variant MODERATE c.1154C>T|p.Thr385Ile S260
33415 BAA01g22780 A01 11524121 C T missense_variant MODERATE c.1834C>T|p.Pro612Ser S198
33416 BAA01g22780 A01 11526498 G A intron_variant MODIFIER c.2269-597G>A| S262
33417 BAA01g22780 A01 11527382 C T synonymous_variant LOW c.2556C>T|p.Pro852Pro S67
33418 BAA01g22780 A01 11527428 G A missense_variant MODERATE c.2602G>A|p.Glu868Lys S287
33419 BAA01g22780 A01 11528597 C T downstream_gene_variant MODIFIER c.*406C>T| S264
33420 BAA01g22780 A01 11528810 C T downstream_gene_variant MODIFIER c.*619C>T| S242
33421 BAA01g22780 A01 11529008 G A downstream_gene_variant MODIFIER c.*817G>A| S276
33422 BAA01g22780 A01 11529139 G A downstream_gene_variant MODIFIER c.*948G>A| S172
S217
33423 BAA01g22780 A01 11529473 G A downstream_gene_variant MODIFIER c.*1282G>A| S301
S304
33424 BAA01g22780 A01 11529517 T A downstream_gene_variant MODIFIER c.*1326T>A| S62
33425 BAA01g22780 A01 11529781 G A downstream_gene_variant MODIFIER c.*1590G>A| S298