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
143101 BAA10g27910 A10 21582653 G A upstream_gene_variant MODIFIER c.-744C>T| S240
143102 BAA10g27910 A10 21582798 G A upstream_gene_variant MODIFIER c.-889C>T| S43
143103 BAA10g27920 A10 21584456 C T missense_variant MODERATE c.722C>T|p.Pro241Leu S111
143104 BAA10g27930 A10 21586755 C T synonymous_variant LOW c.1173G>A|p.Glu391Glu S20
143105 BAA10g27930 A10 21586892 C T missense_variant MODERATE c.1036G>A|p.Ala346Thr S206
S26
143106 BAA10g27930 A10 21587777 G A synonymous_variant LOW c.333C>T|p.Ala111Ala S69
143107 BAA10g27930 A10 21588322 G A upstream_gene_variant MODIFIER c.-213C>T| S240
143108 BAA10g27930 A10 21588709 C T upstream_gene_variant MODIFIER c.-600G>A| S187
143109 BAA10g27930 A10 21589283 G A upstream_gene_variant MODIFIER c.-1174C>T| S239
143110 BAA10g27930 A10 21591627 G A upstream_gene_variant MODIFIER c.-3518C>T| S173
143111 BAA10g27950 A10 21593701 G A synonymous_variant LOW c.129C>T|p.Phe43Phe S245
143112 BAA10g27960 A10 21594416 G A missense_variant MODERATE c.1034C>T|p.Thr345Ile S42
143113 BAA10g27960 A10 21594514 C T synonymous_variant LOW c.936G>A|p.Lys312Lys S295
143114 BAA10g27960 A10 21594555 C T missense_variant MODERATE c.895G>A|p.Glu299Lys S166
143115 BAA10g27950 A10 21597010 G A upstream_gene_variant MODIFIER c.-3181C>T| S261
143116 BAA10g27950 A10 21597116 G A upstream_gene_variant MODIFIER c.-3287C>T| S128
143117 BAA10g27950 A10 21597135 C T upstream_gene_variant MODIFIER c.-3306G>A| S107
143118 BAA10g27950 A10 21597992 C T upstream_gene_variant MODIFIER c.-4163G>A| S232
143119 BAA10g27950 A10 21598113 C T upstream_gene_variant MODIFIER c.-4284G>A| S153
S213
143120 BAA10g27960 A10 21598834 G A upstream_gene_variant MODIFIER c.-3385C>T| S42
143121 BAA10g27970 A10 21599369 G A missense_variant MODERATE c.434G>A|p.Gly145Glu S270
143122 BAA10g27970 A10 21599503 C T synonymous_variant LOW c.568C>T|p.Leu190Leu S8
143123 BAA10g27970 A10 21599573 C T missense_variant MODERATE c.638C>T|p.Ser213Phe S28
143124 BAA10g27970 A10 21599795 G A missense_variant MODERATE c.860G>A|p.Gly287Glu S251
143125 BAA10g27960 A10 21600088 G A upstream_gene_variant MODIFIER c.-4639C>T| S158