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
166651 BAA02g12650 A02 5673094 G A upstream_gene_variant MODIFIER c.-336C>T| S263
166652 BAA02g12650 A02 5674006 G A upstream_gene_variant MODIFIER c.-1248C>T| S239
166653 BAA02g12650 A02 5675465 G A upstream_gene_variant MODIFIER c.-2707C>T| S302
166654 BAA02g12650 A02 5676573 G A upstream_gene_variant MODIFIER c.-3815C>T| S193
166655 BAA02g12650 A02 5677007 G A upstream_gene_variant MODIFIER c.-4249C>T| S197
166656 BAA02g12660 A02 5678891 G A downstream_gene_variant MODIFIER c.*3096C>T| S190
166657 BAA02g12660 A02 5679365 G A downstream_gene_variant MODIFIER c.*2622C>T| S237
166658 BAA02g12660 A02 5679725 G A downstream_gene_variant MODIFIER c.*2262C>T| S144
166659 BAA02g12660 A02 5680481 G A downstream_gene_variant MODIFIER c.*1506C>T| S287
166660 BAA02g12660 A02 5680853 G A downstream_gene_variant MODIFIER c.*1134C>T| S146
166661 BAA02g12660 A02 5682396 G A missense_variant MODERATE c.692C>T|p.Ser231Phe S129
166662 BAA02g12660 A02 5682680 G A synonymous_variant LOW c.408C>T|p.Thr136Thr S109
166663 BAA02g12660 A02 5683592 G A upstream_gene_variant MODIFIER c.-505C>T| S51
166664 BAA02g12670 A02 5685984 C T missense_variant MODERATE c.2671G>A|p.Asp891Asn S219
166665 BAA02g12660 A02 5686310 G A upstream_gene_variant MODIFIER c.-3223C>T| S260
166666 BAA02g12670 A02 5686857 G A synonymous_variant LOW c.2163C>T|p.Phe721Phe S72
S78
166667 BAA02g12670 A02 5687190 C T splice_region_variant&intron_variant LOW c.2027+8G>A| S33
166668 BAA02g12670 A02 5688435 C T synonymous_variant LOW c.1383G>A|p.Lys461Lys S245
166669 BAA02g12670 A02 5688516 C T splice_donor_variant&intron_variant HIGH c.1375+1G>A| S103
166670 BAA02g12680 A02 5688663 C T upstream_gene_variant MODIFIER c.-2738C>T| S255
166671 BAA02g12670 A02 5688770 C T missense_variant MODERATE c.1241G>A|p.Arg414His S100
166672 BAA02g12670 A02 5688801 C T missense_variant MODERATE c.1210G>A|p.Asp404Asn S158
166673 BAA02g12680 A02 5689503 A T upstream_gene_variant MODIFIER c.-1898A>T|
166674 BAA02g12680 A02 5691596 C T synonymous_variant LOW c.196C>T|p.Leu66Leu S157
S163
166675 BAA02g12680 A02 5691793 G A stop_gained HIGH c.393G>A|p.Trp131* S37