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
148851 BAA10g33100 A10 23628994 C T upstream_gene_variant MODIFIER c.-3064C>T| S129
148852 BAA10g33100 A10 23629877 C T upstream_gene_variant MODIFIER c.-2181C>T| S54
148853 BAA10g33090 A10 23630735 C T upstream_gene_variant MODIFIER c.-756G>A| S143
148854 BAA10g33090 A10 23630751 G A upstream_gene_variant MODIFIER c.-772C>T| S50
148855 BAA10g33090 A10 23632308 G A upstream_gene_variant MODIFIER c.-2329C>T| S293
148856 BAA10g33100 A10 23632462 G A missense_variant MODERATE c.227G>A|p.Arg76Lys S165
148857 BAA10g33100 A10 23632691 G A synonymous_variant LOW c.456G>A|p.Ala152Ala S1
S38
S90
148858 BAA10g33090 A10 23633730 G A upstream_gene_variant MODIFIER c.-3751C>T| S125
148859 BAA10g33090 A10 23634650 C T upstream_gene_variant MODIFIER c.-4671G>A| S204
148860 BAA10g33110 A10 23637304 C T missense_variant MODERATE c.4234G>A|p.Glu1412Lys S156
148861 BAA10g33110 A10 23637915 C T missense_variant MODERATE c.3623G>A|p.Ser1208Asn S108
148862 BAA10g33110 A10 23638184 C T synonymous_variant LOW c.3354G>A|p.Gln1118Gln S204
148863 BAA10g33100 A10 23638346 G A downstream_gene_variant MODIFIER c.*2181G>A| S289
S290
148864 BAA10g33110 A10 23638555 C T synonymous_variant LOW c.3066G>A|p.Gly1022Gly S105
148865 BAA10g33110 A10 23639081 C T missense_variant MODERATE c.2540G>A|p.Gly847Glu S255
148866 BAA10g33100 A10 23640039 G A downstream_gene_variant MODIFIER c.*3874G>A| S15
S3
148867 BAA10g33110 A10 23640134 G A missense_variant MODERATE c.1870C>T|p.Arg624Cys S249
148868 BAA10g33100 A10 23640286 C T downstream_gene_variant MODIFIER c.*4121C>T| S218
148869 BAA10g33110 A10 23640385 C T missense_variant MODERATE c.1706G>A|p.Gly569Glu S80
148870 BAA10g33110 A10 23641333 C T missense_variant MODERATE c.1090G>A|p.Glu364Lys S25
148871 BAA10g33110 A10 23641563 G A missense_variant MODERATE c.937C>T|p.Leu313Phe S226
148872 BAA10g33110 A10 23642238 C T missense_variant MODERATE c.523G>A|p.Glu175Lys S292
148873 BAA10g33110 A10 23642725 G A intron_variant MODIFIER c.221-97C>T| S68
148874 BAA10g33110 A10 23642812 G A intron_variant MODIFIER c.221-184C>T| S37
148875 BAA10g33110 A10 23643235 C T intron_variant MODIFIER c.220+108G>A| S82
S92