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
91001 BAA10g00980 A10 471984 C T upstream_gene_variant MODIFIER c.-934G>A| S84
S93
91002 BAA10g00980 A10 472766 G A upstream_gene_variant MODIFIER c.-1716C>T| S251
91003 BAA10g00980 A10 472826 G A upstream_gene_variant MODIFIER c.-1776C>T| S136
91004 BAA10g00980 A10 473170 C T upstream_gene_variant MODIFIER c.-2120G>A| S87
91005 BAA10g00990 A10 475093 G A missense_variant&splice_region_variant MODERATE c.152C>T|p.Pro51Leu S50
91006 BAA10g01010 A10 490819 C T upstream_gene_variant MODIFIER c.-4102G>A| S131
91007 BAA10g01010 A10 491087 C T upstream_gene_variant MODIFIER c.-4370G>A| S44
91008 BAA10g01010 A10 491129 C T upstream_gene_variant MODIFIER c.-4412G>A| S202
91009 BAA10g01010 A10 491145 C T upstream_gene_variant MODIFIER c.-4428G>A| S114
91010 BAA10g01010 A10 491167 C T upstream_gene_variant MODIFIER c.-4450G>A| S225
S73
91011 BAA10g01020 A10 491811 G A upstream_gene_variant MODIFIER c.-1570C>T| S69
91012 BAA10g01020 A10 492754 A T upstream_gene_variant MODIFIER c.-2513T>A| S179
S193
S255
91013 BAA10g01020-BAA10g01030 A10 495787 C T intergenic_region MODIFIER n.495787C>T| S203
91014 BAA10g01020-BAA10g01030 A10 495890 C T intergenic_region MODIFIER n.495890C>T| S117
91015 BAA10g01030 A10 499568 C T downstream_gene_variant MODIFIER c.*2155G>A| S233
91016 BAA10g01060 A10 519490 C T upstream_gene_variant MODIFIER c.-789C>T| S17
S218
S269
91017 BAA10g01060 A10 519816 C A upstream_gene_variant MODIFIER c.-463C>A| S278
91018 BAA10g01060 A10 519972 G A upstream_gene_variant MODIFIER c.-307G>A| S134
91019 BAA10g01060 A10 522322 C T downstream_gene_variant MODIFIER c.*510C>T| S270
91020 BAA10g01070 A10 529377 C T missense_variant MODERATE c.479G>A|p.Gly160Asp S116
91021 BAA10g01070 A10 529766 G A missense_variant MODERATE c.179C>T|p.Pro60Leu S38
91022 BAA10g01070 A10 529802 C T missense_variant MODERATE c.143G>A|p.Arg48Lys S162
91023 BAA10g01070 A10 529979 C T missense_variant MODERATE c.37G>A|p.Ala13Thr S282
91024 BAA10g01070 A10 530144 C T upstream_gene_variant MODIFIER c.-129G>A| S84
S93
91025 BAA10g01080 A10 537492 C T downstream_gene_variant MODIFIER c.*1932G>A| S237