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
101851 BAA10g07320-BAA10g07330 A10 4187977 C T intergenic_region MODIFIER n.4187977C>T| S139
101852 BAA10g07320-BAA10g07330 A10 4188043 C T intergenic_region MODIFIER n.4188043C>T| S297
101853 BAA10g07320-BAA10g07330 A10 4188121 C T intergenic_region MODIFIER n.4188121C>T| S40
101854 BAA10g07320-BAA10g07330 A10 4188127 C T intergenic_region MODIFIER n.4188127C>T| S41
101855 BAA10g07320-BAA10g07330 A10 4189120 C T intergenic_region MODIFIER n.4189120C>T| S10
101856 BAA10g07320-BAA10g07330 A10 4190502 G A intergenic_region MODIFIER n.4190502G>A| S125
101857 BAA10g07320-BAA10g07330 A10 4192363 G A intergenic_region MODIFIER n.4192363G>A| S295
101858 BAA10g07320-BAA10g07330 A10 4192565 G A intergenic_region MODIFIER n.4192565G>A| S302
101859 BAA10g07330 A10 4195278 C T upstream_gene_variant MODIFIER c.-4646C>T| S132
S137
S215
S89
101860 BAA10g07330 A10 4196356 C T upstream_gene_variant MODIFIER c.-3568C>T| S206
S26
101861 BAA10g07330 A10 4196566 G A upstream_gene_variant MODIFIER c.-3358G>A| S15
S3
101862 BAA10g07330 A10 4196634 C T upstream_gene_variant MODIFIER c.-3290C>T| S6
101863 BAA10g07330 A10 4197315 A T upstream_gene_variant MODIFIER c.-2609A>T| S94
101864 BAA10g07340 A10 4200935 G A missense_variant&splice_region_variant MODERATE c.2759C>T|p.Ala920Val S198
101865 BAA10g07330 A10 4201656 C T downstream_gene_variant MODIFIER c.*1291C>T| S9
101866 BAA10g07340 A10 4201971 C T missense_variant MODERATE c.2227G>A|p.Asp743Asn S116
101867 BAA10g07340 A10 4202172 C T missense_variant MODERATE c.2108G>A|p.Arg703Lys S44
101868 BAA10g07340 A10 4203351 C T synonymous_variant LOW c.1377G>A|p.Glu459Glu S235
101869 BAA10g07340 A10 4203561 G A synonymous_variant LOW c.1323C>T|p.Pro441Pro S251
101870 BAA10g07340 A10 4203779 C T missense_variant MODERATE c.1207G>A|p.Gly403Arg S35
101871 BAA10g07340 A10 4203824 C T missense_variant MODERATE c.1162G>A|p.Gly388Arg S188
101872 BAA10g07330 A10 4204386 G A downstream_gene_variant MODIFIER c.*4021G>A| S107
101873 BAA10g07330 A10 4204493 G A downstream_gene_variant MODIFIER c.*4128G>A| S223
101874 BAA10g07340 A10 4205458 C T intron_variant MODIFIER c.1149+663G>A| S84
S93
101875 BAA10g07340 A10 4205678 G A intron_variant MODIFIER c.1149+443C>T| S161