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
157351 BAA02g05060 A02 2221511 C T upstream_gene_variant MODIFIER c.-398G>A| S242
157352 BAA02g05070 A02 2222570 G A missense_variant MODERATE c.446G>A|p.Arg149Lys S51
157353 BAA02g05070 A02 2222995 G A missense_variant MODERATE c.793G>A|p.Asp265Asn S125
157354 BAA02g05060 A02 2223278 C T upstream_gene_variant MODIFIER c.-2165G>A| S71
157355 BAA02g05060 A02 2223658 C T upstream_gene_variant MODIFIER c.-2545G>A| S181
157356 BAA02g05060 A02 2223807 G A upstream_gene_variant MODIFIER c.-2694C>T| S259
157357 BAA02g05060 A02 2225284 C T upstream_gene_variant MODIFIER c.-4171G>A| S195
157358 BAA02g05060 A02 2225995 C T upstream_gene_variant MODIFIER c.-4882G>A| S16
157359 BAA02g05080 A02 2226472 C T missense_variant MODERATE c.433C>T|p.Leu145Phe S58
157360 BAA02g05080 A02 2227096 C T missense_variant&splice_region_variant MODERATE c.496C>T|p.Leu166Phe S131
157361 BAA02g05080 A02 2227127 G A missense_variant MODERATE c.527G>A|p.Arg176Lys S223
157362 BAA02g05070 A02 2227647 G A downstream_gene_variant MODIFIER c.*4617G>A| S23
157363 BAA02g05080 A02 2228359 C T downstream_gene_variant MODIFIER c.*1204C>T| S71
157364 BAA02g05080 A02 2229920 G A downstream_gene_variant MODIFIER c.*2765G>A| S82
S92
157365 BAA02g05090 A02 2231560 C T upstream_gene_variant MODIFIER c.-3604C>T| S243
S299
157366 BAA02g05090 A02 2231832 G A upstream_gene_variant MODIFIER c.-3332G>A| S62
157367 BAA02g05090 A02 2232144 C T upstream_gene_variant MODIFIER c.-3020C>T| S255
157368 BAA02g05090 A02 2234829 G A upstream_gene_variant MODIFIER c.-335G>A| S34
157369 BAA02g05090 A02 2235155 G A upstream_gene_variant MODIFIER c.-9G>A| S209
157370 BAA02g05090 A02 2235458 G A missense_variant MODERATE c.295G>A|p.Asp99Asn S17
157371 BAA02g05090 A02 2235688 G A synonymous_variant LOW c.525G>A|p.Gly175Gly S189
157372 BAA02g05090 A02 2235744 C T missense_variant MODERATE c.581C>T|p.Ser194Phe S298
157373 BAA02g05090 A02 2235944 C T missense_variant MODERATE c.781C>T|p.Pro261Ser S124
157374 BAA02g05090 A02 2236090 G A intron_variant MODIFIER c.834-77G>A| S107
157375 BAA02g05100 A02 2239211 G A upstream_gene_variant MODIFIER c.-3929G>A| S273