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
127251 BAA10g15710 A10 15974041 C T missense_variant MODERATE c.2602G>A|p.Asp868Asn S85
127252 BAA10g15710 A10 15974763 C T missense_variant MODERATE c.1978G>A|p.Asp660Asn S162
127253 BAA10g15710 A10 15975321 C T missense_variant MODERATE c.1420G>A|p.Asp474Asn S297
127254 BAA10g15710 A10 15975349 G A synonymous_variant LOW c.1392C>T|p.Cys464Cys S130
127255 BAA10g15710 A10 15976627 C T missense_variant MODERATE c.475G>A|p.Val159Ile S247
127256 BAA10g15710 A10 15976682 C T synonymous_variant LOW c.420G>A|p.Arg140Arg S173
127257 BAA10g15710 A10 15981719 G A upstream_gene_variant MODIFIER c.-4452C>T| S226
127258 BAA10g15710 A10 15981783 G A upstream_gene_variant MODIFIER c.-4516C>T| S57
127259 BAA10g15710 A10 15982000 C T upstream_gene_variant MODIFIER c.-4733G>A| S28
127260 BAA10g15730 A10 15982320 C T upstream_gene_variant MODIFIER c.-1094C>T| S257
127261 BAA10g15730 A10 15983666 C T splice_region_variant&intron_variant LOW c.8-7C>T| S281
127262 BAA10g15720 A10 15984598 C T downstream_gene_variant MODIFIER c.*3386C>T| S260
127263 BAA10g15740 A10 15984876 C T synonymous_variant LOW c.519C>T|p.Pro173Pro S305
127264 BAA10g15740 A10 15985243 G A splice_donor_variant&intron_variant HIGH c.885+1G>A| S111
127265 BAA10g15740 A10 15985516 C T missense_variant MODERATE c.1073C>T|p.Pro358Leu S242
127266 BAA10g15740 A10 15985577 C T synonymous_variant LOW c.1134C>T|p.Ser378Ser S298
127267 BAA10g15740 A10 15986035 C T synonymous_variant LOW c.1515C>T|p.Thr505Thr S210
S225
127268 BAA10g15740 A10 15986288 C T missense_variant MODERATE c.1702C>T|p.Pro568Ser S19
127269 BAA10g15740 A10 15986438 C T splice_region_variant&intron_variant LOW c.1755-5C>T| S199
127270 BAA10g15740 A10 15986492 G A missense_variant MODERATE c.1804G>A|p.Glu602Lys S69
127271 BAA10g15740 A10 15986679 G A synonymous_variant LOW c.1884G>A|p.Glu628Glu S291
127272 BAA10g15740 A10 15986698 C T missense_variant MODERATE c.1903C>T|p.Leu635Phe S60
127273 BAA10g15740 A10 15986775 C T synonymous_variant LOW c.1980C>T|p.Asp660Asp S124
127274 BAA10g15740 A10 15987168 C T synonymous_variant LOW c.2373C>T|p.Pro791Pro S301
S304
127275 BAA10g15750 A10 15988928 C T synonymous_variant LOW c.1692G>A|p.Glu564Glu S44