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
151751 BAA02g00390 A02 220812 C T downstream_gene_variant MODIFIER c.*2164C>T| S115
151752 BAA02g00400 A02 221016 G A splice_region_variant&intron_variant LOW c.340-8C>T| S62
151753 BAA02g00410 A02 221888 C T upstream_gene_variant MODIFIER c.-4841C>T| S255
151754 BAA02g00400 A02 222752 G A upstream_gene_variant MODIFIER c.-691C>T| S235
151755 BAA02g00400 A02 223884 G A upstream_gene_variant MODIFIER c.-1823C>T| S286
151756 BAA02g00400 A02 224219 G A upstream_gene_variant MODIFIER c.-2158C>T| S246
151757 BAA02g00400 A02 225465 C T upstream_gene_variant MODIFIER c.-3404G>A| S270
151758 BAA02g00400 A02 225659 G A upstream_gene_variant MODIFIER c.-3598C>T| S107
151759 BAA02g00400 A02 226264 A C upstream_gene_variant MODIFIER c.-4203T>G| S153
S213
151760 BAA02g00410 A02 227440 G A missense_variant MODERATE c.712G>A|p.Asp238Asn S172
S202
S217
151761 BAA02g00410 A02 228433 C T synonymous_variant LOW c.985C>T|p.Leu329Leu S193
151762 BAA02g00410 A02 228639 C T intron_variant MODIFIER c.1112+79C>T| S224
151763 BAA02g00410 A02 228986 C T missense_variant MODERATE c.1117C>T|p.Pro373Ser S47
151764 BAA02g00410 A02 229930 G A synonymous_variant LOW c.1650G>A|p.Glu550Glu S122
151765 BAA02g00420 A02 230265 G A upstream_gene_variant MODIFIER c.-3877G>A| S166
151766 BAA02g00420 A02 231133 G A upstream_gene_variant MODIFIER c.-3009G>A| S132
S137
S89
151767 BAA02g00420 A02 231327 G A upstream_gene_variant MODIFIER c.-2815G>A| S69
151768 BAA02g00420 A02 233605 G A upstream_gene_variant MODIFIER c.-537G>A| S271
151769 BAA02g00420 A02 233826 C T upstream_gene_variant MODIFIER c.-316C>T| S281
151770 BAA02g00420 A02 233929 G A upstream_gene_variant MODIFIER c.-213G>A| S48
151771 BAA02g00420 A02 234512 G A splice_region_variant&synonymous_variant LOW c.291G>A|p.Arg97Arg S247
151772 BAA02g00420 A02 235091 C T missense_variant MODERATE c.554C>T|p.Ala185Val S121
151773 BAA02g00420 A02 235285 C T missense_variant MODERATE c.661C>T|p.Leu221Phe S195
151774 BAA02g00420 A02 235528 G A missense_variant MODERATE c.817G>A|p.Glu273Lys S148
S210
S30
S31
151775 BAA02g00430 A02 235779 G A upstream_gene_variant MODIFIER c.-1889G>A| S247