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
168901 BAA02g14070 A02 6604293 C T synonymous_variant LOW c.813C>T|p.Ile271Ile S209
168902 BAA02g14090 A02 6606262 C T upstream_gene_variant MODIFIER c.-3592C>T| S117
168903 BAA02g14080 A02 6606915 G A synonymous_variant LOW c.579C>T|p.Phe193Phe S205
168904 BAA02g14090 A02 6607407 C T upstream_gene_variant MODIFIER c.-2447C>T| S108
168905 BAA02g14080 A02 6609206 G A upstream_gene_variant MODIFIER c.-250C>T| S57
168906 BAA02g14090 A02 6610214 G A missense_variant MODERATE c.208G>A|p.Asp70Asn S303
168907 BAA02g14090 A02 6611419 G A synonymous_variant LOW c.1413G>A|p.Glu471Glu S155
S211
168908 BAA02g14090 A02 6611569 G A synonymous_variant LOW c.1563G>A|p.Glu521Glu S239
168909 BAA02g14090 A02 6611891 G A missense_variant MODERATE c.1885G>A|p.Asp629Asn S79
S91
168910 BAA02g14090 A02 6612037 G A synonymous_variant LOW c.2031G>A|p.Glu677Glu S172
S217
168911 BAA02g14080 A02 6612375 G A upstream_gene_variant MODIFIER c.-3419C>T| S57
168912 BAA02g14100 A02 6615128 C T upstream_gene_variant MODIFIER c.-1212G>A| S183
S198
168913 BAA02g14100 A02 6616426 C T upstream_gene_variant MODIFIER c.-2510G>A| S299
168914 BAA02g14110 A02 6616768 G A missense_variant MODERATE c.584G>A|p.Arg195Lys S298
168915 BAA02g14110 A02 6616786 G A missense_variant MODERATE c.602G>A|p.Gly201Glu S191
168916 BAA02g14110 A02 6616872 G A missense_variant MODERATE c.688G>A|p.Asp230Asn S35
168917 BAA02g14110 A02 6617022 C T synonymous_variant LOW c.747C>T|p.Asn249Asn S13
168918 BAA02g14120 A02 6617575 G A synonymous_variant LOW c.3174C>T|p.Asn1058Asn S228
168919 BAA02g14120 A02 6620320 C T missense_variant MODERATE c.1148G>A|p.Arg383Gln S212
168920 BAA02g14110 A02 6621163 C T downstream_gene_variant MODIFIER c.*4138C>T| S124
168921 BAA02g14110 A02 6621702 G A downstream_gene_variant MODIFIER c.*4677G>A| S282
168922 BAA02g14120 A02 6622252 G A intron_variant MODIFIER c.888-1575C>T| S265
168923 BAA02g14120 A02 6622364 A T intron_variant MODIFIER c.888-1687T>A| S228
168924 BAA02g14120 A02 6623633 G A intron_variant MODIFIER c.887+1243C>T| S225
168925 BAA02g14130 A02 6623731 G A upstream_gene_variant MODIFIER c.-4999G>A| S146