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
162301 BAA02g09230 A02 4085371 G A missense_variant MODERATE c.1061G>A|p.Gly354Glu S68
162302 BAA02g09220 A02 4085469 C T upstream_gene_variant MODIFIER c.-2748G>A| S94
162303 BAA02g09230 A02 4085650 G A synonymous_variant LOW c.1257G>A|p.Lys419Lys S110
162304 BAA02g09220 A02 4086288 C T upstream_gene_variant MODIFIER c.-3567G>A| S127
162305 BAA02g09240 A02 4086409 G A missense_variant MODERATE c.65G>A|p.Gly22Glu S237
162306 BAA02g09220 A02 4086552 C T upstream_gene_variant MODIFIER c.-3831G>A| S278
162307 BAA02g09240 A02 4086795 G A missense_variant MODERATE c.140G>A|p.Gly47Asp S247
162308 BAA02g09240 A02 4086893 G A missense_variant MODERATE c.238G>A|p.Asp80Asn S244
162309 BAA02g09220 A02 4086975 C T upstream_gene_variant MODIFIER c.-4254G>A| S283
162310 BAA02g09220 A02 4086981 G A upstream_gene_variant MODIFIER c.-4260C>T| S132
S137
S215
162311 BAA02g09220 A02 4087011 C T upstream_gene_variant MODIFIER c.-4290G>A| S54
162312 BAA02g09220 A02 4087199 G A upstream_gene_variant MODIFIER c.-4478C>T| S114
162313 BAA02g09240 A02 4087583 G A missense_variant MODERATE c.604G>A|p.Ala202Thr S303
162314 BAA02g09240 A02 4087619 G A missense_variant MODERATE c.640G>A|p.Asp214Asn S98
162315 BAA02g09250 A02 4089770 G A upstream_gene_variant MODIFIER c.-424C>T| S289
S290
162316 BAA02g09250 A02 4089847 G A upstream_gene_variant MODIFIER c.-501C>T| S59
162317 BAA02g09250 A02 4090601 C T upstream_gene_variant MODIFIER c.-1255G>A| S186
162318 BAA02g09260 A02 4091091 G A missense_variant MODERATE c.1216C>T|p.Leu406Phe S37
162319 BAA02g09260 A02 4091589 G A splice_region_variant&intron_variant LOW c.975+8C>T| S53
S81
162320 BAA02g09260 A02 4092015 C T splice_region_variant&intron_variant LOW c.652-4G>A| S284
162321 BAA02g09260 A02 4093419 G A synonymous_variant LOW c.174C>T|p.Ala58Ala S79
S91
162322 BAA02g09260 A02 4093502 C T missense_variant MODERATE c.91G>A|p.Gly31Arg S262
162323 BAA02g09260 A02 4095243 C T upstream_gene_variant MODIFIER c.-1651G>A| S273
162324 BAA02g09260 A02 4095808 C T upstream_gene_variant MODIFIER c.-2216G>A| S255
162325 BAA02g09270 A02 4097323 G A missense_variant MODERATE c.289G>A|p.Asp97Asn S72