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
112901 BAA10g08670 A10 10624970 G A upstream_gene_variant MODIFIER c.-4290G>A| S71
112902 BAA10g08670 A10 10625273 G T upstream_gene_variant MODIFIER c.-3987G>T| S279
112903 BAA10g08670 A10 10625342 C T upstream_gene_variant MODIFIER c.-3918C>T| S37
112904 BAA10g08670 A10 10625863 G A upstream_gene_variant MODIFIER c.-3397G>A| S13
112905 BAA10g08670 A10 10626017 C T upstream_gene_variant MODIFIER c.-3243C>T| S183
112906 BAA10g08670 A10 10627357 C T upstream_gene_variant MODIFIER c.-1903C>T| S249
112907 BAA10g08670 A10 10628060 C T upstream_gene_variant MODIFIER c.-1200C>T| S114
112908 BAA10g08670 A10 10628091 G A upstream_gene_variant MODIFIER c.-1169G>A| S13
112909 BAA10g08670 A10 10628141 C A upstream_gene_variant MODIFIER c.-1119C>A| S278
112910 BAA10g08670 A10 10628286 C T upstream_gene_variant MODIFIER c.-974C>T| S10
S17
112911 BAA10g08670 A10 10628292 C T upstream_gene_variant MODIFIER c.-968C>T| S48
112912 BAA10g08670 A10 10628352 C T upstream_gene_variant MODIFIER c.-908C>T| S297
112913 BAA10g08670 A10 10628450 C T upstream_gene_variant MODIFIER c.-810C>T| S188
112914 BAA10g08670 A10 10629612 C T missense_variant MODERATE c.353C>T|p.Ser118Phe S86
112915 BAA10g08670 A10 10629844 G A synonymous_variant LOW c.585G>A|p.Ser195Ser S109
112916 BAA10g08670 A10 10629883 G A synonymous_variant LOW c.624G>A|p.Gln208Gln S53
112917 BAA10g08670 A10 10630010 C T splice_region_variant&intron_variant LOW c.744+7C>T| S42
112918 BAA10g08680 A10 10630199 G A downstream_gene_variant MODIFIER c.*2235C>T| S75
S81
112919 BAA10g08680 A10 10630847 C T downstream_gene_variant MODIFIER c.*1587G>A| S142
112920 BAA10g08680 A10 10631081 C T downstream_gene_variant MODIFIER c.*1353G>A| S98
112921 BAA10g08670 A10 10631158 C T synonymous_variant LOW c.1452C>T|p.His484His S200
112922 BAA10g08680 A10 10632650 C T synonymous_variant LOW c.1293G>A|p.Leu431Leu S272
112923 BAA10g08680 A10 10632654 C T missense_variant MODERATE c.1289G>A|p.Arg430Lys S294
112924 BAA10g08680 A10 10632870 G A missense_variant MODERATE c.1073C>T|p.Thr358Met S292
112925 BAA10g08680 A10 10633301 G A synonymous_variant LOW c.642C>T|p.Ile214Ile S271