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
451 BAA01g00320 A01 161861 G A missense_variant MODERATE c.782C>T|p.Pro261Leu S44
452 BAA01g00320 A01 161979 C T intron_variant MODIFIER c.769-105G>A| S260
453 BAA01g00320 A01 162153 C T intron_variant MODIFIER c.769-279G>A| S203
454 BAA01g00320 A01 162159 C T intron_variant MODIFIER c.769-285G>A| S100
455 BAA01g00320 A01 162358 G A intron_variant MODIFIER c.769-484C>T| S83
S88
456 BAA01g00320 A01 162410 G A intron_variant MODIFIER c.769-536C>T| S244
457 BAA01g00320 A01 162495 C T intron_variant MODIFIER c.769-621G>A| S64
458 BAA01g00320 A01 162560 G A intron_variant MODIFIER c.769-686C>T| S75
459 BAA01g00330 A01 163036 G A downstream_gene_variant MODIFIER c.*4742C>T| S245
460 BAA01g00330 A01 163177 G A downstream_gene_variant MODIFIER c.*4601C>T| S185
461 BAA01g00330 A01 163323 G A downstream_gene_variant MODIFIER c.*4455C>T| S251
462 BAA01g00330 A01 163765 G A downstream_gene_variant MODIFIER c.*4013C>T| S162
463 BAA01g00330 A01 163777 C T downstream_gene_variant MODIFIER c.*4001G>A| S41
464 BAA01g00330 A01 163909 C T downstream_gene_variant MODIFIER c.*3869G>A| S140
465 BAA01g00330 A01 163989 C T downstream_gene_variant MODIFIER c.*3789G>A| S282
466 BAA01g00330 A01 164105 C T downstream_gene_variant MODIFIER c.*3673G>A| S192
467 BAA01g00320 A01 164616 C T missense_variant MODERATE c.536G>A|p.Cys179Tyr S246
468 BAA01g00320 A01 164618 C T synonymous_variant LOW c.534G>A|p.Ser178Ser S128
469 BAA01g00320 A01 164622 G A missense_variant MODERATE c.530C>T|p.Pro177Leu S296
470 BAA01g00320 A01 164856 G A missense_variant MODERATE c.296C>T|p.Pro99Leu S89
471 BAA01g00330 A01 165002 A G downstream_gene_variant MODIFIER c.*2776T>C| S194
472 BAA01g00330 A01 165104 C T downstream_gene_variant MODIFIER c.*2674G>A| S278
473 BAA01g00330 A01 165289 G T downstream_gene_variant MODIFIER c.*2489C>A| S134
S152
S186
S192
S196
S199
S215
S47
S58
S95
474 BAA01g00330 A01 168087 C T synonymous_variant LOW c.2889G>A|p.Lys963Lys S111
475 BAA01g00330 A01 168171 C T stop_gained HIGH c.2805G>A|p.Trp935* S107