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
98601 BAA10g06020 A10 3107529 G A upstream_gene_variant MODIFIER c.-1953C>T| S306
S308
98602 BAA10g06020 A10 3107558 G A upstream_gene_variant MODIFIER c.-1982C>T| S212
98603 BAA10g06020 A10 3107617 C T upstream_gene_variant MODIFIER c.-2041G>A| S177
98604 BAA10g06020 A10 3108241 C T upstream_gene_variant MODIFIER c.-2665G>A| S19
98605 BAA10g06030 A10 3108674 G A missense_variant MODERATE c.356G>A|p.Gly119Asp S208
S219
98606 BAA10g06020 A10 3109732 C T upstream_gene_variant MODIFIER c.-4156G>A| S73
S91
98607 BAA10g06040 A10 3110068 C T missense_variant MODERATE c.1336G>A|p.Ala446Thr S143
98608 BAA10g06030 A10 3110965 G A downstream_gene_variant MODIFIER c.*1475G>A| S125
98609 BAA10g06040 A10 3111009 G A missense_variant MODERATE c.673C>T|p.Pro225Ser S292
98610 BAA10g06040 A10 3111396 G A splice_region_variant&intron_variant LOW c.350+8C>T| S278
98611 BAA10g06040 A10 3112490 C T upstream_gene_variant MODIFIER c.-397G>A| S260
98612 BAA10g06040 A10 3113116 C T upstream_gene_variant MODIFIER c.-1023G>A| S272
98613 BAA10g06050 A10 3113577 C T synonymous_variant LOW c.1539G>A|p.Thr513Thr S247
98614 BAA10g06050 A10 3113753 G A stop_gained HIGH c.1363C>T|p.Gln455* S216
98615 BAA10g06050 A10 3115182 C T missense_variant MODERATE c.308G>A|p.Arg103Gln S176
98616 BAA10g06040 A10 3115695 G A upstream_gene_variant MODIFIER c.-3602C>T| S212
98617 BAA10g06040 A10 3115857 G A upstream_gene_variant MODIFIER c.-3764C>T| S278
98618 BAA10g06040 A10 3116385 C T upstream_gene_variant MODIFIER c.-4292G>A|
98619 BAA10g06040 A10 3116819 G A upstream_gene_variant MODIFIER c.-4726C>T| S158
98620 BAA10g06040 A10 3116974 A C upstream_gene_variant MODIFIER c.-4881T>G| S116
S215
S228
S252
S275
98621 BAA10g06040 A10 3117079 C T upstream_gene_variant MODIFIER c.-4986G>A| S144
98622 BAA10g06060 A10 3117680 C T missense_variant MODERATE c.167C>T|p.Ser56Phe S170
98623 BAA10g06060 A10 3117872 G A missense_variant MODERATE c.359G>A|p.Gly120Glu S18
98624 BAA10g06060 A10 3117917 G A missense_variant MODERATE c.404G>A|p.Arg135His S136
98625 BAA10g06060 A10 3118548 G A stop_gained HIGH c.1035G>A|p.Trp345* S240