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
134001 BAA10g20300 A10 18316987 C T upstream_gene_variant MODIFIER c.-2856G>A| S185
134002 BAA10g20310 A10 18320075 G A missense_variant MODERATE c.149C>T|p.Ala50Val S61
134003 BAA10g20310 A10 18320980 G A upstream_gene_variant MODIFIER c.-668C>T| S69
134004 BAA10g20310 A10 18323171 G A upstream_gene_variant MODIFIER c.-2859C>T| S223
134005 BAA10g20320 A10 18323634 G A missense_variant MODERATE c.824G>A|p.Gly275Glu S278
134006 BAA10g20310 A10 18323835 C T upstream_gene_variant MODIFIER c.-3523G>A| S268
134007 BAA10g20310 A10 18325106 C T upstream_gene_variant MODIFIER c.-4794G>A| S27
S39
134008 BAA10g20320 A10 18326805 C T downstream_gene_variant MODIFIER c.*3080C>T| S308
134009 BAA10g20320 A10 18327606 G A downstream_gene_variant MODIFIER c.*3881G>A| S139
134010 BAA10g20320 A10 18327745 C T downstream_gene_variant MODIFIER c.*4020C>T| S255
134011 BAA10g20330 A10 18330495 C T upstream_gene_variant MODIFIER c.-2358C>T| S244
134012 BAA10g20330 A10 18330572 C T upstream_gene_variant MODIFIER c.-2281C>T| S221
134013 BAA10g20330 A10 18331567 G A upstream_gene_variant MODIFIER c.-1286G>A| S160
134014 BAA10g20330 A10 18333226 G A missense_variant MODERATE c.163G>A|p.Glu55Lys S42
134015 BAA10g20330 A10 18333906 C T intron_variant MODIFIER c.582+33C>T| S122
134016 BAA10g20330 A10 18334345 G A intron_variant MODIFIER c.656-28G>A| S9
134017 BAA10g20330 A10 18335328 C T intron_variant MODIFIER c.999+238C>T| S157
S163
134018 BAA10g20330 A10 18335920 G A synonymous_variant LOW c.1134G>A|p.Glu378Glu S33
134019 BAA10g20330 A10 18336253 G A intron_variant MODIFIER c.1226+241G>A| S298
134020 BAA10g20330 A10 18336655 G A stop_gained HIGH c.1326G>A|p.Trp442* S212
134021 BAA10g20330 A10 18337707 G A synonymous_variant LOW c.1995G>A|p.Pro665Pro S46
134022 BAA10g20330 A10 18339261 C T missense_variant MODERATE c.3062C>T|p.Ala1021Val S161
134023 BAA10g20330 A10 18339385 C T synonymous_variant LOW c.3096C>T|p.Leu1032Leu S77
134024 BAA10g20330 A10 18339404 G A missense_variant MODERATE c.3115G>A|p.Glu1039Lys S272
134025 BAA10g20330 A10 18340012 C T missense_variant MODERATE c.3482C>T|p.Ala1161Val S26