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
194501 BAA02g27970 A02 15755024 C T upstream_gene_variant MODIFIER c.-1273C>T| S167
194502 BAA02g27970 A02 15755669 G A upstream_gene_variant MODIFIER c.-628G>A| S251
194503 BAA02g27970 A02 15755726 G A upstream_gene_variant MODIFIER c.-571G>A| S260
194504 BAA02g27970 A02 15755745 C T upstream_gene_variant MODIFIER c.-552C>T| S110
S162
194505 BAA02g27970 A02 15755764 C T upstream_gene_variant MODIFIER c.-533C>T| S226
194506 BAA02g27970 A02 15755998 C T upstream_gene_variant MODIFIER c.-299C>T| S52
194507 BAA02g27970 A02 15756568 G A synonymous_variant LOW c.192G>A|p.Ser64Ser S125
194508 BAA02g27980 A02 15757552 G A upstream_gene_variant MODIFIER c.-764G>A| S38
194509 BAA02g27970 A02 15757607 C T synonymous_variant LOW c.804C>T|p.Arg268Arg S63
194510 BAA02g27970 A02 15757624 G A missense_variant MODERATE c.821G>A|p.Gly274Glu S302
194511 BAA02g27980 A02 15759591 C T synonymous_variant LOW c.261C>T|p.Tyr87Tyr S289
S290
194512 BAA02g27980 A02 15759631 C T stop_gained HIGH c.301C>T|p.Arg101* S51
194513 BAA02g27980 A02 15759649 G A missense_variant MODERATE c.319G>A|p.Asp107Asn S189
194514 BAA02g27980 A02 15760512 C T splice_region_variant&intron_variant LOW c.586-4C>T| S142
194515 BAA02g27980 A02 15760576 G A missense_variant MODERATE c.646G>A|p.Glu216Lys S126
194516 BAA02g27970 A02 15761983 C T downstream_gene_variant MODIFIER c.*4115C>T| S164
194517 BAA02g27970 A02 15762022 C T downstream_gene_variant MODIFIER c.*4154C>T| S180
194518 BAA02g27980 A02 15764636 C T synonymous_variant LOW c.2616C>T|p.Asp872Asp S185
194519 BAA02g27980 A02 15765254 C T downstream_gene_variant MODIFIER c.*537C>T| S264
194520 BAA02g27990 A02 15765452 C T missense_variant MODERATE c.1055G>A|p.Cys352Tyr S299
194521 BAA02g27990 A02 15765693 C T missense_variant MODERATE c.901G>A|p.Gly301Arg S177
194522 BAA02g27990 A02 15765714 C T missense_variant MODERATE c.880G>A|p.Glu294Lys S8
194523 BAA02g27990 A02 15766256 C T missense_variant MODERATE c.503G>A|p.Ser168Asn S308
194524 BAA02g27990 A02 15766359 C T missense_variant MODERATE c.400G>A|p.Val134Ile S87
194525 BAA02g27990 A02 15766395 C T missense_variant MODERATE c.364G>A|p.Asp122Asn S250