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
130101 BAA10g17760 A10 16954948 G A upstream_gene_variant MODIFIER c.-2100G>A| S167
130102 BAA10g17760 A10 16955583 G A upstream_gene_variant MODIFIER c.-1465G>A| S131
130103 BAA10g17760 A10 16956009 G A upstream_gene_variant MODIFIER c.-1039G>A| S178
130104 BAA10g17760 A10 16956082 C T upstream_gene_variant MODIFIER c.-966C>T| S92
130105 BAA10g17760 A10 16956532 C T upstream_gene_variant MODIFIER c.-516C>T| S187
130106 BAA10g17760 A10 16956707 G A upstream_gene_variant MODIFIER c.-341G>A| S139
130107 BAA10g17760 A10 16957771 G A stop_gained HIGH c.534G>A|p.Trp178* S264
130108 BAA10g17750 A10 16958158 C T downstream_gene_variant MODIFIER c.*4932C>T| S48
130109 BAA10g17760 A10 16958304 C T synonymous_variant LOW c.762C>T|p.Val254Val S281
130110 BAA10g17760 A10 16958424 C T splice_region_variant&intron_variant LOW c.874+8C>T| S149
130111 BAA10g17760 A10 16958677 C T synonymous_variant LOW c.1038C>T|p.Val346Val S46
130112 BAA10g17760 A10 16958695 G A synonymous_variant LOW c.1056G>A|p.Leu352Leu S88
130113 BAA10g17760 A10 16958830 G A synonymous_variant LOW c.1101G>A|p.Arg367Arg S181
130114 BAA10g17760 A10 16958977 C T splice_region_variant&intron_variant LOW c.1162-4C>T| S173
130115 BAA10g17770 A10 16959453 C T downstream_gene_variant MODIFIER c.*3163G>A| S83
S88
130116 BAA10g17760 A10 16959548 C T missense_variant MODERATE c.1466C>T|p.Ser489Phe S203
130117 BAA10g17770 A10 16961501 G A downstream_gene_variant MODIFIER c.*1115C>T| S203
130118 BAA10g17760 A10 16962205 C T downstream_gene_variant MODIFIER c.*384C>T| S81
S85
130119 BAA10g17770 A10 16962635 G A missense_variant MODERATE c.1091C>T|p.Thr364Ile S3
130120 BAA10g17770 A10 16963012 C T missense_variant MODERATE c.799G>A|p.Val267Ile S283
130121 BAA10g17770 A10 16963280 G A synonymous_variant LOW c.531C>T|p.Ile177Ile S195
130122 BAA10g17770 A10 16963693 G A synonymous_variant LOW c.237C>T|p.Leu79Leu S286
130123 BAA10g17790 A10 16963993 C T upstream_gene_variant MODIFIER c.-4453C>T| S238
130124 BAA10g17770 A10 16964367 C T upstream_gene_variant MODIFIER c.-124G>A| S130
130125 BAA10g17770 A10 16964660 C T upstream_gene_variant MODIFIER c.-417G>A| S50