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
148901 BAA10g33110 A10 23643387 C T missense_variant MODERATE c.176G>A|p.Gly59Glu S44
148902 BAA10g33110 A10 23645541 G A upstream_gene_variant MODIFIER c.-1979C>T| S171
148903 BAA10g33110 A10 23647699 G A upstream_gene_variant MODIFIER c.-4137C>T| S71
148904 BAA10g33120 A10 23649206 G A upstream_gene_variant MODIFIER c.-4380G>A| S271
148905 BAA10g33120 A10 23649209 C A upstream_gene_variant MODIFIER c.-4377C>A| S192
148906 BAA10g33120 A10 23653282 C T upstream_gene_variant MODIFIER c.-304C>T| S295
148907 BAA10g33120 A10 23653498 T A upstream_gene_variant MODIFIER c.-88T>A| S186
148908 BAA10g33130 A10 23654023 C T upstream_gene_variant MODIFIER c.-1631C>T| S262
148909 BAA10g33130 A10 23654135 C T upstream_gene_variant MODIFIER c.-1519C>T| S238
148910 BAA10g33130 A10 23656252 G A synonymous_variant LOW c.405G>A|p.Val135Val S139
148911 BAA10g33120 A10 23657405 C T downstream_gene_variant MODIFIER c.*2040C>T| S236
148912 BAA10g33120 A10 23657451 G A downstream_gene_variant MODIFIER c.*2086G>A| S228
148913 BAA10g33140 A10 23657473 C T stop_gained&splice_region_variant HIGH c.866G>A|p.Trp289* S297
148914 BAA10g33120 A10 23658022 C T downstream_gene_variant MODIFIER c.*2657C>T| S272
148915 BAA10g33140 A10 23658756 C T stop_gained HIGH c.42G>A|p.Trp14* S177
148916 BAA10g33140 A10 23659360 C T upstream_gene_variant MODIFIER c.-563G>A| S210
148917 BAA10g33150 A10 23660266 C T missense_variant MODERATE c.3379G>A|p.Val1127Ile S152
148918 BAA10g33150 A10 23660421 C T missense_variant MODERATE c.3224G>A|p.Arg1075Lys S234
148919 BAA10g33150 A10 23661012 C T missense_variant MODERATE c.2633G>A|p.Arg878Lys S287
148920 BAA10g33150 A10 23661218 C T synonymous_variant LOW c.2427G>A|p.Ser809Ser S200
148921 BAA10g33150 A10 23661793 C T missense_variant MODERATE c.1931G>A|p.Arg644Lys S266
148922 BAA10g33150 A10 23661893 C T missense_variant MODERATE c.1831G>A|p.Glu611Lys S234
148923 BAA10g33150 A10 23662215 C T missense_variant MODERATE c.1585G>A|p.Glu529Lys S262
148924 BAA10g33140 A10 23662538 C T upstream_gene_variant MODIFIER c.-3741G>A| S11
148925 BAA10g33150 A10 23663720 C T missense_variant MODERATE c.740G>A|p.Ser247Asn S292