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
137001 BAA10g22680 A10 19403619 G A upstream_gene_variant MODIFIER c.-4463C>T| S178
137002 BAA10g22710 A10 19404467 C T upstream_gene_variant MODIFIER c.-761C>T| S292
137003 BAA10g22720 A10 19405431 G A upstream_gene_variant MODIFIER c.-3031G>A| S202
137004 BAA10g22710 A10 19405607 G A synonymous_variant LOW c.204G>A|p.Glu68Glu S113
137005 BAA10g22720 A10 19405945 C T upstream_gene_variant MODIFIER c.-2517C>T| S187
137006 BAA10g22720 A10 19407442 C T upstream_gene_variant MODIFIER c.-1020C>T| S107
137007 BAA10g22710 A10 19409062 C T downstream_gene_variant MODIFIER c.*2770C>T| S257
137008 BAA10g22730 A10 19409759 C T stop_gained HIGH c.1389G>A|p.Trp463* S297
137009 BAA10g22730 A10 19410109 C T missense_variant MODERATE c.1039G>A|p.Glu347Lys S234
137010 BAA10g22730 A10 19410739 C T missense_variant MODERATE c.409G>A|p.Asp137Asn S23
137011 BAA10g22730 A10 19411053 C T missense_variant MODERATE c.95G>A|p.Arg32Lys S54
137012 BAA10g22710 A10 19411249 C T downstream_gene_variant MODIFIER c.*4957C>T| S294
137013 BAA10g22730 A10 19411504 G A upstream_gene_variant MODIFIER c.-173C>T| S279
137014 BAA10g22740 A10 19411943 G A synonymous_variant LOW c.898C>T|p.Leu300Leu S163
137015 BAA10g22740 A10 19412518 C T synonymous_variant LOW c.489G>A|p.Glu163Glu S170
137016 BAA10g22740 A10 19412552 C T missense_variant MODERATE c.455G>A|p.Gly152Glu S189
137017 BAA10g22740 A10 19413040 G A missense_variant MODERATE c.206C>T|p.Ala69Val S42
137018 BAA10g22730 A10 19414118 G A upstream_gene_variant MODIFIER c.-2787C>T| S163
137019 BAA10g22730 A10 19414667 C T upstream_gene_variant MODIFIER c.-3336G>A| S46
137020 BAA10g22750 A10 19416119 C T splice_donor_variant&intron_variant HIGH c.392+1G>A| S42
137021 BAA10g22750 A10 19416442 G A missense_variant MODERATE c.311C>T|p.Ser104Phe S132
S137
S215
137022 BAA10g22750 A10 19416625 G A missense_variant MODERATE c.128C>T|p.Ser43Phe S207
137023 BAA10g22750 A10 19416663 C T synonymous_variant LOW c.90G>A|p.Ser30Ser S13
S168
S219
137024 BAA10g22740 A10 19417276 G A upstream_gene_variant MODIFIER c.-3873C>T| S279
137025 BAA10g22760 A10 19417807 G A splice_donor_variant&intron_variant HIGH c.86+1G>A| S62