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
194651 BAA02g28050 A02 15799711 G A upstream_gene_variant MODIFIER c.-321G>A| S37
194652 BAA02g28050 A02 15800086 C T missense_variant MODERATE c.55C>T|p.Leu19Phe S142
194653 BAA02g28050 A02 15800322 G A synonymous_variant LOW c.291G>A|p.Glu97Glu S251
194654 BAA02g28050 A02 15800470 C T missense_variant MODERATE c.439C>T|p.Arg147Cys S216
194655 BAA02g28060 A02 15801469 C T synonymous_variant LOW c.939G>A|p.Gln313Gln S64
194656 BAA02g28060 A02 15801851 G A missense_variant MODERATE c.638C>T|p.Thr213Ile S95
194657 BAA02g28060 A02 15804111 G A upstream_gene_variant MODIFIER c.-1562C>T| S174
S27
194658 BAA02g28060 A02 15804385 C T upstream_gene_variant MODIFIER c.-1836G>A| S207
194659 BAA02g28060 A02 15805030 G A upstream_gene_variant MODIFIER c.-2481C>T| S99
194660 BAA02g28060 A02 15805105 C T upstream_gene_variant MODIFIER c.-2556G>A| S164
194661 BAA02g28060 A02 15805494 G A upstream_gene_variant MODIFIER c.-2945C>T| S256
194662 BAA02g28060 A02 15805502 G A upstream_gene_variant MODIFIER c.-2953C>T| S270
194663 BAA02g28060 A02 15805505 C T upstream_gene_variant MODIFIER c.-2956G>A| S201
194664 BAA02g28060 A02 15805979 C T upstream_gene_variant MODIFIER c.-3430G>A| S81
S85
194665 BAA02g28060 A02 15806279 G A upstream_gene_variant MODIFIER c.-3730C>T| S215
194666 BAA02g28060 A02 15806727 C T upstream_gene_variant MODIFIER c.-4178G>A| S79
194667 BAA02g28060 A02 15806758 C T upstream_gene_variant MODIFIER c.-4209G>A| S242
194668 BAA02g28080 A02 15806855 G A missense_variant MODERATE c.29G>A|p.Arg10Lys S286
194669 BAA02g28080 A02 15806912 C T missense_variant MODERATE c.86C>T|p.Ser29Phe S252
194670 BAA02g28060 A02 15807099 C T upstream_gene_variant MODIFIER c.-4550G>A| S181
194671 BAA02g28080 A02 15807462 G A missense_variant MODERATE c.548G>A|p.Arg183Lys S97
194672 BAA02g28080 A02 15807482 G A splice_donor_variant&intron_variant HIGH c.567+1G>A| S10
S297
194673 BAA02g28080 A02 15807948 C T synonymous_variant LOW c.954C>T|p.Leu318Leu S180
194674 BAA02g28080 A02 15808001 C T missense_variant MODERATE c.1007C>T|p.Thr336Ile S2
194675 BAA02g28080 A02 15808659 C T missense_variant MODERATE c.1576C>T|p.Arg526Cys S51