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
129251 BAA10g17140 A10 16655329 G A synonymous_variant LOW c.1395G>A|p.Thr465Thr S179
129252 BAA10g17150 A10 16655888 C T upstream_gene_variant MODIFIER c.-1607C>T| S203
129253 BAA10g17150 A10 16656138 G A upstream_gene_variant MODIFIER c.-1357G>A| S160
129254 BAA10g17150 A10 16658399 G A synonymous_variant LOW c.747G>A|p.Ala249Ala S88
129255 BAA10g17150 A10 16658728 G A missense_variant MODERATE c.913G>A|p.Glu305Lys S57
129256 BAA10g17160 A10 16660113 C T upstream_gene_variant MODIFIER c.-761C>T| S246
129257 BAA10g17160 A10 16660467 G A upstream_gene_variant MODIFIER c.-407G>A| S303
129258 BAA10g17160 A10 16662040 C T missense_variant MODERATE c.652C>T|p.Leu218Phe S177
129259 BAA10g17170 A10 16663031 C T upstream_gene_variant MODIFIER c.-151C>T| S152
129260 BAA10g17170 A10 16663196 G A synonymous_variant LOW c.15G>A|p.Lys5Lys S15
S3
129261 BAA10g17170 A10 16664687 G A missense_variant MODERATE c.758G>A|p.Gly253Glu S192
129262 BAA10g17170 A10 16665124 C T synonymous_variant LOW c.996C>T|p.His332His S25
129263 BAA10g17170 A10 16665169 C T synonymous_variant LOW c.1041C>T|p.Leu347Leu S275
129264 BAA10g17170 A10 16665514 C T synonymous_variant LOW c.1299C>T|p.Ser433Ser S87
129265 BAA10g17180 A10 16665637 G A upstream_gene_variant MODIFIER c.-1025G>A| S112
129266 BAA10g17180 A10 16666614 G A upstream_gene_variant MODIFIER c.-48G>A| S36
129267 BAA10g17190 A10 16666922 G A upstream_gene_variant MODIFIER c.-1950G>A| S289
S290
129268 BAA10g17180 A10 16667731 C T synonymous_variant LOW c.705C>T|p.Phe235Phe S277
129269 BAA10g17190 A10 16669261 G A missense_variant MODERATE c.226G>A|p.Glu76Lys S157
S163
129270 BAA10g17170 A10 16670399 C T downstream_gene_variant MODIFIER c.*4810C>T| S244
129271 BAA10g17180 A10 16670685 G A downstream_gene_variant MODIFIER c.*2945G>A| S16
129272 BAA10g17180 A10 16671796 G A downstream_gene_variant MODIFIER c.*4056G>A| S7
129273 BAA10g17180 A10 16672072 C T downstream_gene_variant MODIFIER c.*4332C>T| S54
129274 BAA10g17180 A10 16672170 G A downstream_gene_variant MODIFIER c.*4430G>A| S252
129275 BAA10g17200 A10 16675321 C T upstream_gene_variant MODIFIER c.-2482C>T| S149