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
198151 BAA02g29650 A02 16991227 G A downstream_gene_variant MODIFIER c.*1015C>T| S116
198152 BAA02g29650 A02 16992503 G A missense_variant MODERATE c.647C>T|p.Ser216Leu S171
198153 BAA02g29650 A02 16993003 T A intron_variant MODIFIER c.604-457A>T| S188
198154 BAA02g29650 A02 16993625 G A stop_gained HIGH c.559C>T|p.Gln187* S286
198155 BAA02g29650 A02 16993685 G A missense_variant MODERATE c.499C>T|p.Pro167Ser S259
198156 BAA02g29650 A02 16993940 C T missense_variant MODERATE c.244G>A|p.Glu82Lys S108
198157 BAA02g29650 A02 16994146 C T synonymous_variant LOW c.78G>A|p.Arg26Arg S54
198158 BAA02g29650 A02 16994252 G A upstream_gene_variant MODIFIER c.-29C>T| S5
198159 BAA02g29650 A02 16994400 C T upstream_gene_variant MODIFIER c.-177G>A| S183
S198
198160 BAA02g29650 A02 16994654 G A upstream_gene_variant MODIFIER c.-431C>T| S139
S19
198161 BAA02g29650 A02 16995621 G A upstream_gene_variant MODIFIER c.-1398C>T| S298
198162 BAA02g29650 A02 16995652 G A upstream_gene_variant MODIFIER c.-1429C>T| S157
S166
S167
198163 BAA02g29650 A02 16996020 C T upstream_gene_variant MODIFIER c.-1797G>A| S108
198164 BAA02g29650 A02 16997201 G A upstream_gene_variant MODIFIER c.-2978C>T| S148
S210
198165 BAA02g29650 A02 16997391 G A upstream_gene_variant MODIFIER c.-3168C>T| S209
198166 BAA02g29650 A02 16998218 G A upstream_gene_variant MODIFIER c.-3995C>T| S155
S211
198167 BAA02g29650 A02 16998242 G A upstream_gene_variant MODIFIER c.-4019C>T| S259
198168 BAA02g29650 A02 16998587 C T upstream_gene_variant MODIFIER c.-4364G>A| S112
198169 BAA02g29660 A02 16998997 C T missense_variant MODERATE c.1102G>A|p.Ala368Thr S181
198170 BAA02g29660 A02 16999083 C T splice_region_variant&intron_variant LOW c.1024-8G>A| S157
S163
198171 BAA02g29660 A02 16999442 C T intron_variant MODIFIER c.1024-367G>A| S66
198172 BAA02g29660 A02 17000090 C T intron_variant MODIFIER c.1024-1015G>A| S167
198173 BAA02g29660 A02 17002581 C T missense_variant MODERATE c.449G>A|p.Gly150Glu S303
198174 BAA02g29660 A02 17003341 C T synonymous_variant LOW c.87G>A|p.Val29Val S159
S188
S243
S276
S298
S299
198175 BAA02g29660 A02 17003831 G A upstream_gene_variant MODIFIER c.-404C>T| S161