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
143001 BAA10g27840 A10 21556473 G A splice_region_variant&intron_variant LOW c.76+4G>A| S216
143002 BAA10g27840 A10 21556665 G A synonymous_variant LOW c.189G>A|p.Ala63Ala S142
143003 BAA10g27850 A10 21557292 G A upstream_gene_variant MODIFIER c.-1517G>A| S58
143004 BAA10g27850 A10 21557427 C T upstream_gene_variant MODIFIER c.-1382C>T| S229
143005 BAA10g27850 A10 21557513 C T upstream_gene_variant MODIFIER c.-1296C>T| S105
143006 BAA10g27850 A10 21557673 G A upstream_gene_variant MODIFIER c.-1136G>A| S74
143007 BAA10g27850 A10 21557877 G A upstream_gene_variant MODIFIER c.-932G>A| S18
143008 BAA10g27850 A10 21558002 C T upstream_gene_variant MODIFIER c.-807C>T| S182
143009 BAA10g27860 A10 21558981 C T upstream_gene_variant MODIFIER c.-1667C>T| S157
S163
143010 BAA10g27850 A10 21559046 C T missense_variant MODERATE c.137C>T|p.Ser46Phe S48
143011 BAA10g27850 A10 21559056 G A synonymous_variant LOW c.147G>A|p.Lys49Lys S271
143012 BAA10g27850 A10 21559290 G A synonymous_variant LOW c.381G>A|p.Glu127Glu S118
143013 BAA10g27860 A10 21559509 G A upstream_gene_variant MODIFIER c.-1139G>A| S219
S72
143014 BAA10g27860 A10 21559678 C T upstream_gene_variant MODIFIER c.-970C>T| S69
143015 BAA10g27860 A10 21561454 C T missense_variant MODERATE c.685C>T|p.Leu229Phe S238
143016 BAA10g27860 A10 21561757 C T synonymous_variant LOW c.988C>T|p.Leu330Leu S262
143017 BAA10g27870 A10 21562803 G A upstream_gene_variant MODIFIER c.-603G>A| S184
143018 BAA10g27870 A10 21563941 G A missense_variant MODERATE c.421G>A|p.Gly141Arg S240
143019 BAA10g27870 A10 21565099 G A missense_variant MODERATE c.1225G>A|p.Val409Ile S298
143020 BAA10g27880 A10 21565809 G A missense_variant MODERATE c.325G>A|p.Glu109Lys S298
143021 BAA10g27880 A10 21565987 C T missense_variant MODERATE c.503C>T|p.Ser168Phe S67
143022 BAA10g27880 A10 21567782 C T synonymous_variant LOW c.2298C>T|p.Cys766Cys S196
143023 BAA10g27890 A10 21568252 G A upstream_gene_variant MODIFIER c.-1160G>A| S139
143024 BAA10g27890 A10 21568798 C T upstream_gene_variant MODIFIER c.-614C>T| S250
143025 BAA10g27870 A10 21569513 C T downstream_gene_variant MODIFIER c.*4331C>T| S186