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
130601 BAA10g18140 A10 17120558 C T upstream_gene_variant MODIFIER c.-3984C>T| S12
130602 BAA10g18140 A10 17120719 G A upstream_gene_variant MODIFIER c.-3823G>A| S205
130603 BAA10g18140 A10 17120758 G A upstream_gene_variant MODIFIER c.-3784G>A| S166
130604 BAA10g18140 A10 17120896 G A upstream_gene_variant MODIFIER c.-3646G>A| S226
130605 BAA10g18140 A10 17120908 C T upstream_gene_variant MODIFIER c.-3634C>T| S113
130606 BAA10g18140 A10 17121072 G A upstream_gene_variant MODIFIER c.-3470G>A| S166
130607 BAA10g18140 A10 17121694 C T upstream_gene_variant MODIFIER c.-2848C>T| S210
130608 BAA10g18140 A10 17122293 G A upstream_gene_variant MODIFIER c.-2249G>A| S4
130609 BAA10g18140 A10 17123119 C T upstream_gene_variant MODIFIER c.-1423C>T| S153
S213
130610 BAA10g18130 A10 17123598 G A missense_variant MODERATE c.671C>T|p.Ala224Val S288
130611 BAA10g18130 A10 17123735 C T synonymous_variant LOW c.534G>A|p.Glu178Glu S299
130612 BAA10g18130 A10 17124207 G A missense_variant MODERATE c.62C>T|p.Ser21Leu S298
130613 BAA10g18140 A10 17124874 C T synonymous_variant LOW c.333C>T|p.Phe111Phe S148
S30
S31
130614 BAA10g18140 A10 17125233 C T missense_variant MODERATE c.692C>T|p.Thr231Met S23
130615 BAA10g18130 A10 17125981 G A upstream_gene_variant MODIFIER c.-1713C>T| S35
130616 BAA10g18130 A10 17126063 C T upstream_gene_variant MODIFIER c.-1795G>A| S197
130617 BAA10g18130 A10 17126777 C T upstream_gene_variant MODIFIER c.-2509G>A| S225
S73
130618 BAA10g18150 A10 17127804 G A missense_variant MODERATE c.961G>A|p.Glu321Lys S292
130619 BAA10g18150 A10 17128589 G A synonymous_variant LOW c.1746G>A|p.Glu582Glu S255
130620 BAA10g18170 A10 17130372 C T synonymous_variant LOW c.378G>A|p.Lys126Lys S256
130621 BAA10g18160 A10 17130578 G A upstream_gene_variant MODIFIER c.-719C>T| S151
S263
130622 BAA10g18170 A10 17130831 C T synonymous_variant LOW c.24G>A|p.Gln8Gln S251
130623 BAA10g18160 A10 17131151 C T upstream_gene_variant MODIFIER c.-1292G>A| S174
S216
S241
S265
130624 BAA10g18180 A10 17131487 C T missense_variant MODERATE c.481G>A|p.Asp161Asn S195
130625 BAA10g18180 A10 17132176 G A synonymous_variant LOW c.49C>T|p.Leu17Leu S65