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
168351 BAA02g13660 A02 6369741 G C upstream_gene_variant MODIFIER c.-2087C>G| S240
168352 BAA02g13670 A02 6370057 C T stop_gained HIGH c.1107G>A|p.Trp369* S44
168353 BAA02g13670 A02 6370912 G A synonymous_variant LOW c.342C>T|p.Ile114Ile S189
168354 BAA02g13680 A02 6375266 G A missense_variant MODERATE c.25G>A|p.Glu9Lys S294
168355 BAA02g13670 A02 6375396 C T upstream_gene_variant MODIFIER c.-3881G>A| S181
168356 BAA02g13690 A02 6377591 G A synonymous_variant LOW c.186G>A|p.Lys62Lys S302
168357 BAA02g13700 A02 6378560 G A upstream_gene_variant MODIFIER c.-1155G>A| S259
168358 BAA02g13700 A02 6378995 C T upstream_gene_variant MODIFIER c.-720C>T| S306
168359 BAA02g13700 A02 6380743 C T stop_gained HIGH c.499C>T|p.Gln167* S233
168360 BAA02g13690 A02 6381217 C T downstream_gene_variant MODIFIER c.*3623C>T| S165
168361 BAA02g13690 A02 6381252 C T downstream_gene_variant MODIFIER c.*3658C>T| S70
168362 BAA02g13700 A02 6381682 C T missense_variant MODERATE c.908C>T|p.Ser303Phe S135
168363 BAA02g13690 A02 6382260 C T downstream_gene_variant MODIFIER c.*4666C>T| S292
168364 BAA02g13700 A02 6383317 G A downstream_gene_variant MODIFIER c.*1583G>A| S193
168365 BAA02g13710 A02 6383991 C T missense_variant MODERATE c.1199G>A|p.Gly400Asp S299
168366 BAA02g13700 A02 6384563 C T downstream_gene_variant MODIFIER c.*2829C>T| S128
168367 BAA02g13700 A02 6384614 G A downstream_gene_variant MODIFIER c.*2880G>A| S52
168368 BAA02g13710 A02 6384805 C T missense_variant MODERATE c.925G>A|p.Glu309Lys S266
168369 BAA02g13710 A02 6385190 C T missense_variant MODERATE c.620G>A|p.Gly207Glu S201
S94
168370 BAA02g13710 A02 6385209 C T missense_variant MODERATE c.601G>A|p.Glu201Lys S212
168371 BAA02g13700 A02 6385432 G A downstream_gene_variant MODIFIER c.*3698G>A| S217
S248
168372 BAA02g13700 A02 6385882 G A downstream_gene_variant MODIFIER c.*4148G>A| S296
168373 BAA02g13710 A02 6386581 C T upstream_gene_variant MODIFIER c.-321G>A| S116
168374 BAA02g13710 A02 6387124 G A upstream_gene_variant MODIFIER c.-864C>T| S48
168375 BAA02g13710 A02 6387617 C T upstream_gene_variant MODIFIER c.-1357G>A| S169