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
136001 BAA10g21730 A10 19002162 G A synonymous_variant LOW c.693C>T|p.Phe231Phe S202
136002 BAA10g21730 A10 19002320 C T missense_variant MODERATE c.535G>A|p.Glu179Lys S48
136003 BAA10g21720 A10 19003231 G A downstream_gene_variant MODIFIER c.*2756G>A| S62
136004 BAA10g21730 A10 19003624 C T upstream_gene_variant MODIFIER c.-189G>A| S153
136005 BAA10g21730 A10 19005982 C T upstream_gene_variant MODIFIER c.-2547G>A| S51
136006 BAA10g21730 A10 19006502 C T upstream_gene_variant MODIFIER c.-3067G>A| S25
136007 BAA10g21730 A10 19007869 G A upstream_gene_variant MODIFIER c.-4434C>T| S263
S80
136008 BAA10g21730 A10 19008061 C T upstream_gene_variant MODIFIER c.-4626G>A| S76
136009 BAA10g21730 A10 19008340 G A upstream_gene_variant MODIFIER c.-4905C>T| S195
136010 BAA10g21730-BAA10g21740 A10 19009840 G A intergenic_region MODIFIER n.19009840G>A| S163
136011 BAA10g21730-BAA10g21740 A10 19009853 C T intergenic_region MODIFIER n.19009853C>T| S194
136012 BAA10g21740 A10 19010090 C T upstream_gene_variant MODIFIER c.-4780C>T| S23
136013 BAA10g21740 A10 19011788 C T upstream_gene_variant MODIFIER c.-3082C>T| S200
136014 BAA10g21740 A10 19011902 G A upstream_gene_variant MODIFIER c.-2968G>A| S127
136015 BAA10g21740 A10 19013287 C T upstream_gene_variant MODIFIER c.-1583C>T| S37
136016 BAA10g21740 A10 19013446 G A upstream_gene_variant MODIFIER c.-1424G>A| S270
136017 BAA10g21740 A10 19014012 G A upstream_gene_variant MODIFIER c.-858G>A| S223
136018 BAA10g21740 A10 19014723 C G upstream_gene_variant MODIFIER c.-147C>G| S119
136019 BAA10g21740 A10 19014829 G A upstream_gene_variant MODIFIER c.-41G>A| S202
136020 BAA10g21750 A10 19015477 C T upstream_gene_variant MODIFIER c.-1007C>T| S183
136021 BAA10g21750 A10 19016178 C T upstream_gene_variant MODIFIER c.-306C>T| S52
136022 BAA10g21750 A10 19017091 C T synonymous_variant LOW c.237C>T|p.Arg79Arg S10
136023 BAA10g21750 A10 19017883 G A synonymous_variant LOW c.630G>A|p.Lys210Lys S263
136024 BAA10g21760 A10 19020427 C T missense_variant MODERATE c.1275G>A|p.Met425Ile S188
136025 BAA10g21750 A10 19020712 C T downstream_gene_variant MODIFIER c.*802C>T| S28