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
129001 BAA10g16990-BAA10g17000 A10 16569900 C T intergenic_region MODIFIER n.16569900C>T| S277
129002 BAA10g16990-BAA10g17000 A10 16570272 G A intergenic_region MODIFIER n.16570272G>A| S192
129003 BAA10g16990-BAA10g17000 A10 16570417 G A intergenic_region MODIFIER n.16570417G>A| S62
129004 BAA10g16990-BAA10g17000 A10 16570472 G A intergenic_region MODIFIER n.16570472G>A| S64
129005 BAA10g16990-BAA10g17000 A10 16570484 G A intergenic_region MODIFIER n.16570484G>A| S198
129006 BAA10g17000 A10 16574582 G A upstream_gene_variant MODIFIER c.-2216G>A| S163
129007 BAA10g17000 A10 16576899 G A synonymous_variant LOW c.102G>A|p.Arg34Arg S166
129008 BAA10g17000 A10 16576953 T C synonymous_variant LOW c.156T>C|p.Asp52Asp S26
129009 BAA10g17010 A10 16579180 G A upstream_gene_variant MODIFIER c.-102C>T| S186
129010 BAA10g17010 A10 16579872 C T upstream_gene_variant MODIFIER c.-794G>A| S2
S213
S3
S4
S6
129011 BAA10g17010 A10 16580269 C T upstream_gene_variant MODIFIER c.-1191G>A| S48
129012 BAA10g17010 A10 16581849 C T upstream_gene_variant MODIFIER c.-2771G>A| S235
129013 BAA10g17020 A10 16583621 G A missense_variant MODERATE c.1064C>T|p.Ser355Phe S148
S30
S31
129014 BAA10g17020 A10 16583663 C T missense_variant MODERATE c.1022G>A|p.Arg341Lys S23
129015 BAA10g17020 A10 16583727 G A missense_variant MODERATE c.958C>T|p.Pro320Ser S127
129016 BAA10g17020 A10 16583814 G A missense_variant MODERATE c.871C>T|p.Pro291Ser S155
129017 BAA10g17020 A10 16583864 C T missense_variant MODERATE c.821G>A|p.Ser274Asn S133
129018 BAA10g17020 A10 16585827 G A intron_variant MODIFIER c.598-1660C>T| S16
129019 BAA10g17020 A10 16586009 G C intron_variant MODIFIER c.598-1842C>G| S182
S292
S36
129020 BAA10g17020 A10 16586360 T A intron_variant MODIFIER c.598-2193A>T| S153
S236
S257
129021 BAA10g17020 A10 16586568 G A intron_variant MODIFIER c.598-2401C>T| S180
129022 BAA10g17020 A10 16587162 G A intron_variant MODIFIER c.598-2995C>T| S166
129023 BAA10g17020 A10 16587740 C T intron_variant MODIFIER c.597+2785G>A| S297
129024 BAA10g17020 A10 16587743 C T intron_variant MODIFIER c.597+2782G>A| S48
129025 BAA10g17020 A10 16588601 C T intron_variant MODIFIER c.597+1924G>A| S193