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
170551 BAA02g15120 A02 7240697 G A upstream_gene_variant MODIFIER c.-51C>T| S2
170552 BAA02g15120 A02 7240807 G A upstream_gene_variant MODIFIER c.-161C>T| S188
170553 BAA02g15120 A02 7240838 G A upstream_gene_variant MODIFIER c.-192C>T| S256
170554 BAA02g15120 A02 7242978 G A upstream_gene_variant MODIFIER c.-2332C>T| S245
170555 BAA02g15120 A02 7243052 C T upstream_gene_variant MODIFIER c.-2406G>A| S63
170556 BAA02g15120 A02 7243498 C T upstream_gene_variant MODIFIER c.-2852G>A| S244
170557 BAA02g15120 A02 7245382 C T upstream_gene_variant MODIFIER c.-4736G>A| S124
170558 BAA02g15130 A02 7248106 G A upstream_gene_variant MODIFIER c.-408C>T| S183
S198
170559 BAA02g15130 A02 7248800 G A upstream_gene_variant MODIFIER c.-1102C>T| S183
S198
170560 BAA02g15130-BAA02g15140 A02 7253989 G A intergenic_region MODIFIER n.7253989G>A| S56
170561 BAA02g15130-BAA02g15140 A02 7254636 G A intergenic_region MODIFIER n.7254636G>A| S159
S243
170562 BAA02g15130-BAA02g15140 A02 7257198 C T intergenic_region MODIFIER n.7257198C>T| S108
170563 BAA02g15130-BAA02g15140 A02 7257315 G A intergenic_region MODIFIER n.7257315G>A| S11
170564 BAA02g15130-BAA02g15140 A02 7258381 A T intergenic_region MODIFIER n.7258381A>T| S156
170565 BAA02g15130-BAA02g15140 A02 7258476 C T intergenic_region MODIFIER n.7258476C>T| S167
170566 BAA02g15130-BAA02g15140 A02 7259232 C T intergenic_region MODIFIER n.7259232C>T| S203
S224
170567 BAA02g15130-BAA02g15140 A02 7260361 G A intergenic_region MODIFIER n.7260361G>A| S11
170568 BAA02g15130-BAA02g15140 A02 7260675 C T intergenic_region MODIFIER n.7260675C>T| S262
170569 BAA02g15140 A02 7265266 G A downstream_gene_variant MODIFIER c.*1389C>T| S125
170570 BAA02g15140 A02 7265871 G A downstream_gene_variant MODIFIER c.*784C>T| S69
170571 BAA02g15140 A02 7265997 G A downstream_gene_variant MODIFIER c.*658C>T| S7
170572 BAA02g15140 A02 7266460 C T downstream_gene_variant MODIFIER c.*195G>A| S234
170573 BAA02g15140 A02 7267114 C T missense_variant MODERATE c.1045G>A|p.Gly349Ser S262
170574 BAA02g15140 A02 7267123 C T missense_variant MODERATE c.1036G>A|p.Asp346Asn S163
170575 BAA02g15140 A02 7267412 G A intron_variant MODIFIER c.853-15C>T| S169