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
163451 BAA02g10160 A02 4509498 G A missense_variant MODERATE c.1001G>A|p.Ser334Asn S197
163452 BAA02g10160 A02 4509527 C T stop_gained HIGH c.1030C>T|p.Gln344* S240
163453 BAA02g10160 A02 4511180 G A intron_variant MODIFIER c.1680+1003G>A| S302
163454 BAA02g10160 A02 4511296 C T intron_variant MODIFIER c.1681-1045C>T| S224
163455 BAA02g10160 A02 4511347 G A intron_variant MODIFIER c.1681-994G>A| S166
163456 BAA02g10160 A02 4511426 C T intron_variant MODIFIER c.1681-915C>T| S73
S91
163457 BAA02g10160 A02 4511456 G A intron_variant MODIFIER c.1681-885G>A| S303
163458 BAA02g10160 A02 4511464 C T intron_variant MODIFIER c.1681-877C>T| S240
163459 BAA02g10170 A02 4511859 C T upstream_gene_variant MODIFIER c.-4995C>T| S55
163460 BAA02g10170 A02 4511991 G A upstream_gene_variant MODIFIER c.-4863G>A| S287
163461 BAA02g10160 A02 4514982 C T synonymous_variant LOW c.2686C>T|p.Leu896Leu S175
163462 BAA02g10160 A02 4515233 G A missense_variant MODERATE c.2937G>A|p.Met979Ile S283
163463 BAA02g10160 A02 4516948 C T downstream_gene_variant MODIFIER c.*1067C>T| S25
S264
163464 BAA02g10170 A02 4517062 G A missense_variant MODERATE c.13G>A|p.Gly5Arg S45
163465 BAA02g10160 A02 4520509 G A downstream_gene_variant MODIFIER c.*4628G>A| S192
163466 BAA02g10180 A02 4520651 G A missense_variant MODERATE c.2369C>T|p.Ala790Val S164
163467 BAA02g10170 A02 4521315 G A downstream_gene_variant MODIFIER c.*2379G>A| S131
163468 BAA02g10170 A02 4522540 C T downstream_gene_variant MODIFIER c.*3604C>T| S178
163469 BAA02g10170 A02 4522596 G A downstream_gene_variant MODIFIER c.*3660G>A| S87
163470 BAA02g10170 A02 4523097 G A downstream_gene_variant MODIFIER c.*4161G>A| S289
S290
163471 BAA02g10170 A02 4523107 G A downstream_gene_variant MODIFIER c.*4171G>A| S207
163472 BAA02g10180 A02 4523395 G A synonymous_variant LOW c.1620C>T|p.Pro540Pro S48
163473 BAA02g10180 A02 4524169 C T splice_region_variant&synonymous_variant LOW c.1113G>A|p.Ser371Ser S178
163474 BAA02g10180 A02 4524542 C T missense_variant MODERATE c.908G>A|p.Ser303Asn S25
163475 BAA02g10180 A02 4525364 G A missense_variant MODERATE c.404C>T|p.Ala135Val S125