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
177901 BAA02g19050 A02 9867738 G A downstream_gene_variant MODIFIER c.*1604C>T| S247
177902 BAA02g19050 A02 9867863 C T downstream_gene_variant MODIFIER c.*1479G>A| S246
177903 BAA02g19050 A02 9867999 G A downstream_gene_variant MODIFIER c.*1343C>T| S13
177904 BAA02g19050 A02 9869003 G A downstream_gene_variant MODIFIER c.*339C>T| S278
177905 BAA02g19050 A02 9869247 C T downstream_gene_variant MODIFIER c.*95G>A| S233
177906 BAA02g19050 A02 9869398 C T missense_variant MODERATE c.1810G>A|p.Glu604Lys S77
S82
177907 BAA02g19050 A02 9870774 G A missense_variant MODERATE c.1097C>T|p.Ser366Phe S76
177908 BAA02g19060 A02 9871212 G A downstream_gene_variant MODIFIER c.*4263C>T| S296
177909 BAA02g19050 A02 9872302 C T missense_variant MODERATE c.247G>A|p.Glu83Lys S178
177910 BAA02g19050 A02 9872313 G A missense_variant MODERATE c.236C>T|p.Ser79Phe S238
177911 BAA02g19050 A02 9873544 C T upstream_gene_variant MODIFIER c.-731G>A| S202
177912 BAA02g19060 A02 9876222 C T missense_variant MODERATE c.857G>A|p.Gly286Glu S275
177913 BAA02g19060 A02 9877062 C T synonymous_variant LOW c.252G>A|p.Glu84Glu S177
177914 BAA02g19050 A02 9877401 T C upstream_gene_variant MODIFIER c.-4588A>G| S179
177915 BAA02g19050 A02 9877732 C T upstream_gene_variant MODIFIER c.-4919G>A| S233
177916 BAA02g19060 A02 9879000 C T upstream_gene_variant MODIFIER c.-1305G>A| S270
177917 BAA02g19060 A02 9879183 G A upstream_gene_variant MODIFIER c.-1488C>T| S76
177918 BAA02g19060 A02 9879251 G A upstream_gene_variant MODIFIER c.-1556C>T| S34
177919 BAA02g19060 A02 9879360 G A upstream_gene_variant MODIFIER c.-1665C>T| S231
177920 BAA02g19060 A02 9879489 G A upstream_gene_variant MODIFIER c.-1794C>T| S282
177921 BAA02g19060 A02 9879812 G A upstream_gene_variant MODIFIER c.-2117C>T| S125
177922 BAA02g19060 A02 9880168 G A upstream_gene_variant MODIFIER c.-2473C>T| S50
177923 BAA02g19060 A02 9880503 G A upstream_gene_variant MODIFIER c.-2808C>T| S153
S213
177924 BAA02g19060 A02 9880823 G A upstream_gene_variant MODIFIER c.-3128C>T| S34
177925 BAA02g19060 A02 9880884 G A upstream_gene_variant MODIFIER c.-3189C>T| S296