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
173601 BAA02g16840 A02 8323074 G A downstream_gene_variant MODIFIER c.*236G>A| S23
173602 BAA02g16840 A02 8324347 C T downstream_gene_variant MODIFIER c.*1509C>T| S84
S93
173603 BAA02g16840 A02 8324991 G A downstream_gene_variant MODIFIER c.*2153G>A| S149
S190
173604 BAA02g16840 A02 8327340 G A downstream_gene_variant MODIFIER c.*4502G>A| S69
173605 BAA02g16840 A02 8327655 C T downstream_gene_variant MODIFIER c.*4817C>T| S100
173606 BAA02g16850 A02 8328014 C T downstream_gene_variant MODIFIER c.*1137G>A| S32
173607 BAA02g16850 A02 8328020 G A downstream_gene_variant MODIFIER c.*1131C>T| S41
173608 BAA02g16850 A02 8328199 C T downstream_gene_variant MODIFIER c.*952G>A| S206
S26
173609 BAA02g16850 A02 8328325 G A downstream_gene_variant MODIFIER c.*826C>T| S289
S290
173610 BAA02g16860 A02 8335929 G A upstream_gene_variant MODIFIER c.-1646C>T| S203
173611 BAA02g16860 A02 8335930 A G upstream_gene_variant MODIFIER c.-1647T>C| S182
173612 BAA02g16870 A02 8337890 G A synonymous_variant LOW c.294C>T|p.Phe98Phe S298
173613 BAA02g16870 A02 8339744 G A upstream_gene_variant MODIFIER c.-1561C>T| S56
173614 BAA02g16870 A02 8339878 C T upstream_gene_variant MODIFIER c.-1695G>A| S13
173615 BAA02g16870 A02 8341084 C T upstream_gene_variant MODIFIER c.-2901G>A| S262
173616 BAA02g16880 A02 8343010 G A missense_variant MODERATE c.26G>A|p.Gly9Glu S191
173617 BAA02g16880 A02 8343035 C T synonymous_variant LOW c.51C>T|p.Asn17Asn S18
173618 BAA02g16880 A02 8343091 G A missense_variant&splice_region_variant MODERATE c.107G>A|p.Arg36Gln S50
173619 BAA02g16900 A02 8343953 G A upstream_gene_variant MODIFIER c.-2959G>A| S150
173620 BAA02g16890 A02 8344682 C T missense_variant MODERATE c.791G>A|p.Cys264Tyr S63
173621 BAA02g16890 A02 8344825 C T synonymous_variant LOW c.648G>A|p.Val216Val S281
173622 BAA02g16890 A02 8344879 G A synonymous_variant LOW c.594C>T|p.Ile198Ile S125
173623 BAA02g16890 A02 8346703 G A upstream_gene_variant MODIFIER c.-1231C>T| S276
173624 BAA02g16900 A02 8346926 G A synonymous_variant LOW c.15G>A|p.Gly5Gly S232
173625 BAA02g16900 A02 8347528 C T synonymous_variant LOW c.579C>T|p.Ala193Ala S267