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
201301 BAA02g30740 A02 18102870 C T upstream_gene_variant MODIFIER c.-4639C>T| S224
201302 BAA02g30740 A02 18103054 C T upstream_gene_variant MODIFIER c.-4455C>T| S18
201303 BAA02g30740 A02 18103828 C T upstream_gene_variant MODIFIER c.-3681C>T| S139
201304 BAA02g30740 A02 18104297 C T upstream_gene_variant MODIFIER c.-3212C>T| S112
201305 BAA02g30740 A02 18104432 G A upstream_gene_variant MODIFIER c.-3077G>A| S125
201306 BAA02g30740 A02 18104452 C T upstream_gene_variant MODIFIER c.-3057C>T| S63
201307 BAA02g30740 A02 18104788 C T upstream_gene_variant MODIFIER c.-2721C>T| S87
201308 BAA02g30740 A02 18105428 C T upstream_gene_variant MODIFIER c.-2081C>T| S23
201309 BAA02g30740 A02 18105594 G A upstream_gene_variant MODIFIER c.-1915G>A| S12
201310 BAA02g30740 A02 18105947 C T upstream_gene_variant MODIFIER c.-1562C>T| S139
201311 BAA02g30740 A02 18106081 G A upstream_gene_variant MODIFIER c.-1428G>A| S293
201312 BAA02g30740 A02 18107011 G A upstream_gene_variant MODIFIER c.-498G>A| S125
201313 BAA02g30740 A02 18108132 C T synonymous_variant LOW c.624C>T|p.Asp208Asp S18
201314 BAA02g30740 A02 18108572 C T missense_variant MODERATE c.1064C>T|p.Ser355Leu S301
S304
201315 BAA02g30740 A02 18108871 G A missense_variant MODERATE c.1363G>A|p.Glu455Lys S159
S243
201316 BAA02g30750 A02 18109424 G A upstream_gene_variant MODIFIER c.-4867G>A|
201317 BAA02g30750 A02 18111684 C T upstream_gene_variant MODIFIER c.-2607C>T| S19
201318 BAA02g30750 A02 18113287 C T upstream_gene_variant MODIFIER c.-1004C>T| S262
201319 BAA02g30750 A02 18113958 C T upstream_gene_variant MODIFIER c.-333C>T| S206
201320 BAA02g30750 A02 18114065 T G upstream_gene_variant MODIFIER c.-226T>G| S89
201321 BAA02g30750 A02 18114570 G A missense_variant MODERATE c.280G>A|p.Asp94Asn S168
201322 BAA02g30750 A02 18115497 C T stop_gained HIGH c.1207C>T|p.Gln403* S32
201323 BAA02g30750 A02 18116193 G A missense_variant MODERATE c.1798G>A|p.Asp600Asn S13
201324 BAA02g30760 A02 18117580 C T splice_donor_variant&intron_variant HIGH c.1041+1G>A| S303
201325 BAA02g30760 A02 18118610 C T synonymous_variant LOW c.258G>A|p.Lys86Lys S189