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
31151 BAA01g21690 A01 10781689 G A upstream_gene_variant MODIFIER c.-2840C>T| S302
31152 BAA01g21690 A01 10781999 G A upstream_gene_variant MODIFIER c.-3150C>T| S88
31153 BAA01g21690-BAA01g21700 A01 10784018 C T intergenic_region MODIFIER n.10784018C>T| S185
31154 BAA01g21690-BAA01g21700 A01 10784895 C T intergenic_region MODIFIER n.10784895C>T| S121
31155 BAA01g21690-BAA01g21700 A01 10785123 G A intergenic_region MODIFIER n.10785123G>A| S139
31156 BAA01g21700 A01 10786418 G A downstream_gene_variant MODIFIER c.*3942C>T| S280
31157 BAA01g21700 A01 10786569 G A downstream_gene_variant MODIFIER c.*3791C>T| S116
31158 BAA01g21700 A01 10786634 G A downstream_gene_variant MODIFIER c.*3726C>T| S237
31159 BAA01g21700 A01 10787767 C T downstream_gene_variant MODIFIER c.*2593G>A| S148
S210
S30
S31
31160 BAA01g21700 A01 10789602 C T downstream_gene_variant MODIFIER c.*758G>A| S264
31161 BAA01g21700 A01 10789818 C T downstream_gene_variant MODIFIER c.*542G>A| S255
31162 BAA01g21700 A01 10790475 C T missense_variant MODERATE c.206G>A|p.Gly69Glu S63
31163 BAA01g21720 A01 10790574 G A upstream_gene_variant MODIFIER c.-4809G>A| S209
31164 BAA01g21700 A01 10790720 C T synonymous_variant LOW c.27G>A|p.Glu9Glu S210
S225
31165 BAA01g21700 A01 10792613 G A upstream_gene_variant MODIFIER c.-1867C>T| S268
31166 BAA01g21700 A01 10793615 C T upstream_gene_variant MODIFIER c.-2869G>A| S135
31167 BAA01g21700 A01 10794056 C T upstream_gene_variant MODIFIER c.-3310G>A| S41
31168 BAA01g21700 A01 10794163 C T upstream_gene_variant MODIFIER c.-3417G>A| S65
31169 BAA01g21700 A01 10794760 G A upstream_gene_variant MODIFIER c.-4014C>T| S193
31170 BAA01g21720 A01 10795654 T A missense_variant MODERATE c.272T>A|p.Met91Lys S40
S49
31171 BAA01g21720 A01 10795726 C T missense_variant MODERATE c.344C>T|p.Thr115Ile S114
31172 BAA01g21720 A01 10795755 C T missense_variant MODERATE c.373C>T|p.Leu125Phe S279
31173 BAA01g21720 A01 10796017 C T synonymous_variant LOW c.490C>T|p.Leu164Leu S99
31174 BAA01g21710 A01 10796262 C T upstream_gene_variant MODIFIER c.-3164G>A| S155
S211
31175 BAA01g21730 A01 10797912 G A stop_gained HIGH c.36G>A|p.Trp12* S245