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
197201 BAA02g29210 A02 16698902 G A downstream_gene_variant MODIFIER c.*4728G>A| S166
197202 BAA02g29220 A02 16699175 G A downstream_gene_variant MODIFIER c.*3708G>A| S19
197203 BAA02g29220 A02 16699803 C T downstream_gene_variant MODIFIER c.*4336C>T| S1
S90
197204 BAA02g29220 A02 16700160 C T downstream_gene_variant MODIFIER c.*4693C>T| S280
197205 BAA02g29230 A02 16700292 C T missense_variant MODERATE c.2368G>A|p.Gly790Ser S276
197206 BAA02g29230 A02 16700627 G A synonymous_variant LOW c.2115C>T|p.Ile705Ile S187
197207 BAA02g29230 A02 16700685 C T missense_variant MODERATE c.2057G>A|p.Cys686Tyr S40
S49
197208 BAA02g29230 A02 16700816 G A intron_variant MODIFIER c.2019-93C>T| S72
S78
197209 BAA02g29230 A02 16701202 G A intron_variant MODIFIER c.2019-479C>T| S113
S117
S122
S266
S297
S55
S65
S9
197210 BAA02g29230 A02 16701218 C T intron_variant MODIFIER c.2019-495G>A| S299
197211 BAA02g29230 A02 16702224 C T intron_variant MODIFIER c.2019-1501G>A| S219
197212 BAA02g29230 A02 16702704 C T intron_variant MODIFIER c.2019-1981G>A| S64
197213 BAA02g29230 A02 16704835 G A intron_variant MODIFIER c.2018+791C>T| S10
197214 BAA02g29230 A02 16704898 C T intron_variant MODIFIER c.2018+728G>A| S182
197215 BAA02g29230 A02 16704909 G A intron_variant MODIFIER c.2018+717C>T| S35
197216 BAA02g29230 A02 16704960 G A intron_variant MODIFIER c.2018+666C>T| S229
197217 BAA02g29230 A02 16706497 C T intron_variant MODIFIER c.1780-303G>A| S203
197218 BAA02g29240 A02 16707548 C T upstream_gene_variant MODIFIER c.-4017C>T| S182
197219 BAA02g29240 A02 16707550 G A upstream_gene_variant MODIFIER c.-4015G>A| S129
197220 BAA02g29240 A02 16707701 C T upstream_gene_variant MODIFIER c.-3864C>T| S135
197221 BAA02g29230 A02 16708246 C T missense_variant MODERATE c.1411G>A|p.Asp471Asn S11
197222 BAA02g29230 A02 16708394 C T synonymous_variant LOW c.1263G>A|p.Ser421Ser S212
197223 BAA02g29230 A02 16708541 C T synonymous_variant LOW c.1116G>A|p.Gln372Gln S308
197224 BAA02g29230 A02 16708724 G A synonymous_variant LOW c.933C>T|p.Leu311Leu S256
197225 BAA02g29230 A02 16708746 T A missense_variant MODERATE c.911A>T|p.Asp304Val S204