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
192251 BAA02g26820 A02 15028991 G A synonymous_variant LOW c.141G>A|p.Leu47Leu S161
192252 BAA02g26820 A02 15029335 C T synonymous_variant LOW c.396C>T|p.Ile132Ile S138
192253 BAA02g26820 A02 15030307 C T splice_region_variant&intron_variant LOW c.739-3C>T| S144
192254 BAA02g26830 A02 15031413 C T upstream_gene_variant MODIFIER c.-341C>T| S165
S211
S227
192255 BAA02g26820 A02 15033574 C T downstream_gene_variant MODIFIER c.*2716C>T| S2
192256 BAA02g26820 A02 15033923 G A downstream_gene_variant MODIFIER c.*3065G>A| S44
192257 BAA02g26820 A02 15034221 G A downstream_gene_variant MODIFIER c.*3363G>A| S92
192258 BAA02g26830 A02 15036474 A G downstream_gene_variant MODIFIER c.*3330A>G| S165
S211
S227
192259 BAA02g26840 A02 15037789 G A upstream_gene_variant MODIFIER c.-4544G>A| S306
192260 BAA02g26840 A02 15039340 G A upstream_gene_variant MODIFIER c.-2993G>A| S37
192261 BAA02g26840 A02 15040699 C T upstream_gene_variant MODIFIER c.-1634C>T| S277
192262 BAA02g26840 A02 15042317 C T upstream_gene_variant MODIFIER c.-16C>T| S9
192263 BAA02g26850 A02 15042579 G A downstream_gene_variant MODIFIER c.*2455C>T| S241
192264 BAA02g26840 A02 15043670 C T synonymous_variant LOW c.432C>T|p.Ser144Ser S233
192265 BAA02g26840 A02 15043758 C T missense_variant MODERATE c.520C>T|p.Pro174Ser S40
S49
192266 BAA02g26840 A02 15043792 C T missense_variant MODERATE c.554C>T|p.Ser185Phe S18
192267 BAA02g26850 A02 15045547 C T missense_variant MODERATE c.302G>A|p.Ser101Asn S16
192268 BAA02g26850 A02 15046357 G A upstream_gene_variant MODIFIER c.-327C>T| S80
192269 BAA02g26850 A02 15046656 G A upstream_gene_variant MODIFIER c.-626C>T| S291
192270 BAA02g26850 A02 15046728 G A upstream_gene_variant MODIFIER c.-698C>T| S240
192271 BAA02g26860 A02 15047345 C T missense_variant MODERATE c.1130G>A|p.Arg377Lys S170
192272 BAA02g26860 A02 15047387 C T missense_variant MODERATE c.1088G>A|p.Gly363Glu S140
192273 BAA02g26850 A02 15047827 G A upstream_gene_variant MODIFIER c.-1797C>T| S165
192274 BAA02g26850 A02 15048167 C T upstream_gene_variant MODIFIER c.-2137G>A| S117
192275 BAA02g26860 A02 15048404 C T missense_variant MODERATE c.683G>A|p.Gly228Glu S107